Skip to main content
International Journal of Biological Sciences logoLink to International Journal of Biological Sciences
. 2020 Mar 15;16(10):1708–1717. doi: 10.7150/ijbs.45538

Traditional Chinese Medicine in the Treatment of Patients Infected with 2019-New Coronavirus (SARS-CoV-2): A Review and Perspective

Yang Yang 1,*, Md Sahidul Islam 1,*, Jin Wang 1, Yuan Li 1, Xin Chen 1,
PMCID: PMC7098036  PMID: 32226288

Abstract

Currently, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2, formerly known as 2019-nCoV, the causative pathogen of Coronavirus Disease 2019 (COVID-19)) has rapidly spread across China and around the world, causing an outbreak of acute infectious pneumonia. No specific anti-virus drugs or vaccines are available for the treatment of this sudden and lethal disease. The supportive care and non-specific treatment to ameliorate the symptoms of the patient are the only options currently. At the top of these conventional therapies, greater than 85% of SARS-CoV-2 infected patients in China are receiving Traditional Chinese Medicine (TCM) treatment. In this article, relevant published literatures are thoroughly reviewed and current applications of TCM in the treatment of COVID-19 patients are analyzed. Due to the homology in epidemiology, genomics, and pathogenesis of the SARS-CoV-2 and SARS-CoV, and the widely use of TCM in the treatment of SARS-CoV, the clinical evidence showing the beneficial effect of TCM in the treatment of patients with SARS coronaviral infections are discussed. Current experiment studies that provide an insight into the mechanism underlying the therapeutic effect of TCM, and those studies identified novel naturally occurring compounds with anti-coronaviral activity are also introduced.

Keywords: SARS-CoV-2, Traditional Chinese Medicine (TCM), coronavirus pneumonia

Introduction

In December 2019, there was an outbreak of unexplainable pneumonia in Wuhan city, Hubei province, China 1. By Jan 7, 2020, it was confirmed that a new type of coronavirus named SARS-CoV-2 (formerly named as 2019-nCoV) had emerged 2. The World Health Organization (WHO) named the Wuhan pneumonia as Coronavirus Disease-2019 (COVID-19) on Feb 11, 2020 3. The COVID-19 patients showed typical respiratory symptom (such as cough, fever, and lung damage) and some other symptoms such as fatigue, myalgia, and diarrhea 4, 5. As of February 17, 2020, a total of 73,332 cases of the SARS-CoV-2 infected pneumonia has been reported in China and 25 other countries, of which 72,528 cases was found in China 6. Due to the rapid spread of SARS-CoV-2 through human-to-human transmission, the cases currently continue to rise. SARS-CoV-2 extracted from patients with pneumonia in Wuhan is an enveloped single stranded RNA-type beta-coronavirus 7. The genome sequences of SARS-CoV-2 shared 79.5% sequence identity to severe acute respiratory syndrome-related coronaviruses (SARS-CoV) 8, 9. In addition, the spike (S) protein of SARS-CoV-2 and SARS-CoV enters human alveolar epithelial cells through binding angiotensin- converting enzyme 2 (ACE2) receptor 8.

COVID-19 can be diagnosed by either chest CT radiography or a laboratory testing. Unfortunately, specific antiviral drugs or vaccines currently have not been available for the treatment 10, 11. According to the current clinical guideline in China and the experiences in the treatment of SARS or Middle East Respiratory Syndrome (MERS) patients, both conventional medicine and traditional Chinese medicine (TCM) are used for the treatment of patients with infection of SARS-CoV-2 in China 12-14. This review mainly focuses on the discussion of TCM usage in the treatment of COVID-19 patients, in the context of current conventional management. Due to the homology in epidemiology, genomics, and pathogenesis of the SARS-CoV-2 and SARS-CoV 8, 9, and widely usage of TCM in the treatment of patients infected with SARS-CoV in 2002-2003 15, the clinical evidence showing the efficacy and safety of TCM in the treatment of patients with the emerging coronaviral will be summarized and analyzed, including the laboratory studies that provide an insight into molecular basis of therapeutic benefits.

Conventional treatment of SARS-CoV-2: is there a room for Chinese medicine?

Due to the absence of a specific antiviral therapeutics and vaccine, main treatment strategy for COVID-19 is supportive care, which is supplemented by the combination of broad-spectrum antibiotics, antivirals, corticosteroids and convalescent plasma 16 (Table 1). HIV protease inhibitors ritonavir and lopinavir have been used, typically in combination with appropriate antibiotics or with IFNα-2b, in the treatment of SARS-CoV-2 infected patients 7, 17. Nucleoside analogs such as ribavirin 12 may be potentially beneficial for the treatment of COVID-19, since ribavirin was approved for treating respiratory syncytial virus (RSV) infection 18 and used extensively during the SARS and MERS outbreak 10. However, ribavirin had severe side effects such as anemia 18 and whether it had sufficient antiviral activity against SARS-CoV-2 is unclear. Nucleoside analogs favipiravir (T-705) can effectively inhibit the activity of RNA polymerase of RNA viruses such as influenza 19. A recent in vitro study found that it had the anti-SARS-CoV-2 activity 20, but the in vivo effect remains elusive. Remdesivir may be the most promising antiviral drug for treating COVID-19. It has in vitro and in vivo antiviral activity against a wide array of RNA viruses including SARS and MERS 21, and could decrease viral loads and pathology of lungs in animal models 22. A study showed remdesivir markedly inhibited the infection of SARS-CoV-2 in Vero E6 cells 20, and most symptoms of the first US patient infected with SARS-CoV-2 had resolved swiftly after intravenous administration with remdesivir 23. Currently, it is under clinical trial to evaluate the safety and efficacy of intravenous remdesivir for patients with SARS-CoV-2 infection 24. Oral oseltamivir has been used for the treatment of the cases with SARS-CoV-2 7, while its efficacy currently remains uncertain.

Table 1.

Conventional treatment of patients with SARS-CoV-2 infection

Type of treatment Therapeutic agent or device Reference
Oxygen therapy

Nasal cannula
Non-invasive mechanical ventilation
Invasive mechanical ventilation
ECMO*
16
Antibiotics combination Amoxicillin
Azithromycin
Fluoroquinolones
16
Antivirals


Lopinavir/ ritonavir 16, 17
Ribavirin 16, 18
Favipiravir (T-705) 19, 20
Remdesivir 20-23
Oseltamivir 7
Chloroquine 20, 36
Interferon 7, 17
Corticosteroids Methylprednisolone 7
Convalescent plasma Convalescent plasma 22

*ECMO, extracorporeal membrane oxygenation.

Host-targeted small molecules approved for other human diseases may modulate the virus-host interactions of SARS-CoV-2. Chloroquine, a potential broad-spectrum antiviral drug 25, 26, was shown by a recent study had anti-SARS-CoV-2 activity 20. Its clinical efficacy is under study in an open-label trial (ChiCTR2000029609) 12. IFNα (5 million U) atomization inhalation was recommended as antiviral therapy to treat SARS-CoV-2 16. A trial testing IFNα-2b combination of the approved anti-HCV inhibitors has been initiated 17, however, whether it could act synergistically against SARS-CoV-2 is unclear.

Corticosteroids were frequently used to suppress the elevated cytokine levels in patients with SARS-CoV 27, 28 and MERS-CoV 29, 30. However, there are no evidence showing that the mortality of SARS and MERS patients was reduced by the treatment with corticosteroids, while the clearance of viral was delayed by such treatment 31-33. Consequently, corticosteroids are not suggested to systemically use in SARS-CoV-2 infected patients 34, 35.

Previously, it was shown that, either in severe influenza or SARS-CoV infection, convalescent plasma treatment could significantly decrease viral load and reduce the mortality 31, 36. Convalescent plasma has been used for severe SARS-CoV-2 infection in China 22, although promising, the efficacy and safety need to be carefully further evaluated.

Consistent with previous analysis, WHO also concluded "to date, there is no specific medicine recommended to prevent or treat SARS-CoV-2" 37. TCM has been used in control of infectious diseases for thousands of years. There is a clear room for the intervention of TCM as a complementary therapy for COVID-19 patients. It is reported that the patients with SARS-CoV infection have benefited from TCM treatment 38, including amelioration of side effect of conventional therapeutics 39, 40. Based on these factors, there is a general expectation that TCM would be a valuable weapon in the armory against SARS-CoV-2.

Traditional Chinese Medicine in the treatment of patients infected with SARS-CoV: clinical evidence

Application of TCM in the treatment of SARS-CoV-2 is largely inspired by the treatment of SARS caused by outbreak of SARS coronavirus (SARS-CoV) in the late of 2002 in the Guangdong Province of China which spread rapidly during the 2003, with the cumulative number worldwide of over 8,000 41-43. Ranging from case reports, case series, controlled observational studies and randomized clinical trials, clinical studies aiming to examine the effect of TCM on SARS have been carried out and reported. There are quite compelling evidences support the notion that TCM has beneficial effect in the treatment or prevention of SARS. For example, the rate of fatality in Hong Kong and Singapore was approximately 18%, while the rate for Beijing was initially more than 52% until the 5th of May and decreased gradually to 4%-1% after the 20th of May in 2003. The dramatic reduced fatality from late May in Beijing was believed to be associated with the use of TCM as a supplement to the conventional therapy 44. Lau and colleagues reported that, during SARS outbreak, 1063 volunteers including 926 hospital workers and 37 laboratory technicians working in high-risk virus laboratories used a TCM herbal extract, namely Sang Ju Yin plus Yu Ping Feng San. Compared with the 0.4% of infection in the control group, none of TCM users infected. Furthermore, there was some evidence that Sang Ju Yin plus Yu Ping Feng San could modulate T cells in a manner to enhance host defense capacity 45, 46. In a controlled clinical study, the supplementary treatment with TCM resulted in marked improvement of symptoms and shortened the disease course 47. The clinical beneficial effect of TCM appears to be supported by laboratory studies. For example, a high-profile research published in the Lancet reported that glycyrrhizin, a major active constituent liquorice root which is the most frequently used Chinese herb, potently inhibited the replication of clinical isolates of SARS virus 48. Another independent study confirmed the antivirus activity of glycyrrhizin by plaque reduction assays and this study found that another Chinese herbal compound baicalin also had the anti-SARS activity 49. Furthermore, Wang et al. found MOL376, a compound derived from TCM, may become a lead compound for SARS therapy by inhibition of cathepsin L, a target for the treatment of SARS 50.

There is a myriad of literature on TCM treatments for SARS published after the SARS epidemic in China. A critical analysis of these publications would be useful to confirm the beneficial effect of TCM. Liu et al. systematically reviewed eight randomized controlled trials, and concluded that, by combination with conventional medicine, TCM showed the beneficial effects such as decrease of mortality and relief of symptom, as well as control of fungal infections in patients with SARS. However, the evidence is not sufficient enough due to the poor quality of methodology used in the trials 13. Leung analyzed 90 peer-reviewed papers with reasonable quality from 130 publications and concluded that TCM used together with conventional treatment had some positive effects, including better control of fever, quicker clearance of chest infection and other symptoms. However, such beneficial effect of TCM is not conclusive and more high-quality clinical studies are required 15. In another thorough literature analysis, Liu and colleagues concluded that there was no benefit of adjuvant treatment with TCM in terms of mortality 39. Due to the lack of high quality TCM trials and biases that influenced the validity of results, Wu and colleagues suggested to re-run clinical trials of TCM for the treatment of acute respiratory tract infections (ARTIs) 51.

Identification of anti-novel coronaviral compound from Traditional Chinese Medicine

Natural products used in TCM remains to be a wealthy source for the identification of novel therapeutic agents for the treatment of human diseases 52. In the past decade, scientists have made a considerable effort to identify multiple component herbal formulae in TCM with anti-SARS-CoV activity (Table 2). Further identification of chemical entities contained in TCM herbs responsible for the anti-SARS- CoV effect was also pursued (Table 3). Due to the homology of SARS-CoV and SARS-CoV-2, these previous studies may shed light on the naturally occurring compounds with the capacity to inhibit SARS-CoV-2.

Table 2.

TCM herb formulae used for the Treatment of SARS-CoV infection

TCM Formula Composition Therapeutics effect Reference
Yin Qiao San Fructus Forsythiae, Flos Lonicerae, Radix Platycodonis, Herba Menthae, Herba Lophatheri, Radix Glycyrrhizae, Herba Schizonepetae, Fermented soybean, Fructus arctii, and Rhizoma Phragmitis “Disperses wind-heat, clears heat, and relieves toxicity”, according to TCM theory
Treatment of upper respiratory tract infection.
Improvement of the function of upper respiratory mucosal immune system
111, 112
Yu Ping Feng San Astragali radix, Astragalus membranaceus, Atractylodes macrocephala, and Saposhnikoviae Radix “Tonifying qi” to protect from external pathogens”, according to TCM theory
Reportedly have antiviral, anti-inflammatory and immunoregulatory effects
113-115
Sang Ju Yin and Yu Ping Feng San Sang Ju Yin [made with chrysanthemum, mulberry leaf, and 6 other herbs] and Yu Ping Feng San Reportedly have anti-viral and immunoregulatory effects 46
Lian Hua Qing Wen Capsule
Forsythia suspensa, Ephedra sinica, Lonicera japonica, Isatis indigotica, Mentha haplocalyx, Dryopteris crassirhizoma, Rhodiola rosea, Gypsum Fibrosum, Pogostemon cablin, Rheum palmatum , Houttuynia cordata, Glycyrrhizae, uralensis, and Armeniaca sibirica “Clear heat and detoxify, removes lung hotness”, according to TCM theory
Reportedly have antiviral, anti-inflammatory and immunoregulatory effects.
82, 83
Shuang Huang Lian Lonicera japonica, Scutellaria baicalensis, and Forsythia suspensa “Clear heat and detoxify, remove lung hotness”, according to TCM theory
Reportedly has anti-SARS-CoV-2 activity
Reportedly has immunosuppressive effects
78, 80, 116
Ma Xin Gan Shi Tang
Ephedrae herba, Armeniacae semenamarum), Glycyrrhizae radix et rhizome, Gypsum fibrosum, and Da Yuan Yin [Arecae semen, Magnoliae officinalis cortex, Tsaoko fructus,Anemarrhenae rhizoma, Dioscoreae rhizoma, Scutellariae radix, and Glycyrrhizae raadix et rhizome] “Facilitate the flow of the lung “qi” and clear away heat”, according to TCM theory
Reportedly have anti-SARS-CoV activity
117, 118

Table 3.

TCM herbal extracts or TCM-derived Compounds with anti-HCoV Activity

TCM Compound (s) Mode of action Reference
Plant-derived phenolic compounds and Root extract of Isatis indigotica Inhibit the cleavage activity of SARS-3CLpro enzyme 57
Water extract of Houttuynia cordata Inhibit the viral SARS-3CLpro activity
Block viral RNA‑dependent RNA polymerase activity (RdRp)
Immunomodulation
54, 55
Scutellarein and myricetin Inhibit nsP13 by affecting the ATPase activity 61
Glycyrrhizin from Glycyrrhizae radix Inhibit viral adsorption and penetration 48, 75
Herbacetin, quercetin, isobavaschalcone, 3‐β‐D‐glucoside and helichrysetin Inhibit cleavage activity of MERS-3CLpro enzyme 60
Tetrandrine, fangchinoline, and cepharanthine Inhibit the expression of HCoV- OC43 spike and nucleocapsid protein.
Immunomodulation
106, 119
Chinese Rhubarb extracts Inhibit SARS-3CLpro activity 53
Flavonoids (For example: extracted from litchi seeds, herbacetin, rhoifolin, pectolinarin, quercetin, epigallocatechin gallate, and gallocatechin gallate) Inhibit SARS-3CLpro activity 56, 58, 59
Quercetin and TSL-1 from Toona sinensis Roem Inhibit the cellular entry of SARS-CoV 76
Emodin derived from genus Rheum and Polygonum Inhibit interaction of SARS-CoV Spike protein and ACE2
Inhibit the 3a ion channel of coronavirus SARS‐CoV and HCoV‐OC43
67, 72
Kaempferol derivatives Inhibit 3a ion channel of coronavirus 73
Baicalin from Scutellaria baicalensis Inhibit Angiotensin-converting enzyme (ACE) 44, 68
Saikosaponins Prevent the early stage of HCoV‑22E9 infection, including viral attachment and penetration 74
Tetra-O-galloyl-β-D-glucose and luteolin, from Galla chinensis and Veronicalina riifolia respectively Avidly binds with surface spike protein of SARS-CoV 71

3- chymotrypsin-like protease (3CLpro) is vital for replication of virus, and thus represents a promising drug target for the development of therapeutics agents for SARS-CoV as well as other human coronaviruses including SARS-CoV-2. It was reported that following TCM herbal extracts had the capacity to inhibit the enzymatic activity of SARS 3CLpro: Chinese Rhubarb extracts (IC50: 13.76 ± 0.03 μg/mL) 53, water extract of Houttuynia cordata 54, 55, flavonoid extracted from litchi seeds 56 and beta-sitosterol (IC50: 1210µM) extracted from the root extract of Isatis indigotica 57. Further, following herb-derived naturally occurring compounds including sinigrin (IC50: 217µM), indigo (IC50: 752µM), aloe-emodin (IC50: 366 µM), hesperetin (IC50:8.3 µM) 57, quercetin (IC50: 73µM), epigallocatechin gallate (IC50: 73µM), gallocatechin gallate (IC50: 47 µM) 58, herbacetin, rhoifolin and pectolinarin 59 were able to inhibit the SARS 3CLpro activity. Moreover, the flavonoids namely herbacetin, isobavaschalcone, quercetin 3‐β‐D‐glucoside, and helichrysetin had the potential to block the enzymatic activity of MERS‐CoV 3CL protease 60.

The helicase protein is also considered as a potential target for the development of anti-HCoV (human coronavirus) agents. Yu et al. reported scutellarein and myricetin potently inhibited the nsP13 (SARS-CoV helicase protein) in vitro by affecting the ATPase activity 61. The RNA- dependent RNA polymerase (RdRp), a key enzyme responsible for both positive and negative-strand RNA synthesis, also represents another potential druggable target. It was shown that the extracts of Kang Du Bu Fei Tang (IC50:471.3 µg/mL), Sinomenium acutum (IC50:198.6 µg/mL), Coriolus versicolor (IC50:108.4 µg/mL) and Ganoderma lucidum (IC50:41.9 µg/mL) inhibited SARS-CoV RdRp in a dose- dependent manner 54. Wu et al. performed large- scale screening of existing drugs, natural products, and synthetic compounds (>10000 compounds) to identify effective anti-SARS-CoV agents through a cell-based assay with SARS virus and Vero E6 cells 62. They found that ginsenoside-Rb1 isolated from Panax ginseng, aescin isolated from the horse chestnut tree, reserpine contained in the genus Rauwolfia and extracts of eucalyptus and Lonicera japonica inhibited SARS-CoV replication at non-toxic concentrations 62.

Same as SARS-CoV and HCoV-NL63, SARS-CoV-2 uses host receptor ACE2 for the cellular entrance 63-66. Therefore, TCM with the capacity to target ACE2 holds the promise to prevent the infection of SARS-CoV-2. Emodin from genus Rheum and Polygonum 67, baicalin from in Scutellaria baicalensis 44, 68, nicotianamine from foodstuff (especially “soybean ACE2 inhibitor (ACE2iSB)”) 69, scutellarin 70, tetra-O-galloyl-β-D-glucose (TGG) from Galla chinensis and luteolin from Veronicalina riifolia 71 markedly inhibited the interaction of SARS-CoV S-protein and ACE2. However, the anti-SARS-CoV activity of these compounds remain to be evaluated. In addition, inhibition of the 3a ion channel by emodin 72 or kaempferol derivatives- juglanin 73 could potentially prevent the viral release from the infected cells. Saikosaponins 74, glycyrrhizin 48, 75, quercetin and TSL-1 extracted from Toona sinensis Roem 76 purportedly had potent anti-SARS-CoV effects by inhibition of viral cellular entry, adsorption, and penetration.

Overwhelming inflammatory responses are attributable to the deaths of patients with infection of SARS-CoV, or MERS-CoV, or COVID-19. Thus, anti-inflammatory agents presumably could reduce the severity and mortality rate 77. Shuang Huang Lian, a TCM herbal product prepared from Lonicerae japonicae Flos, Scutellariae radix and Fructus Forsythiae, purportedly had the activity to inhibit SARS-CoV-2 78. Interestingly, We have shown that this herbal preparation potently inhibited staphylococcal toxic shock syndrome toxin 1 (TSST-1)-induced production of cytokines (IL-1β, IL-6, TNF-α, IFN-γ) and chemokines (MIP-1α, MIP-1β and MCP-1) by peripheral blood mononuclear cell (PBMC) 79. In line with our results, this herbal product was shown to markedly reduced the transcriptional and translational levels of inflammatory cytokines TNF-α, IL-1β, and IL-6 in lipopolysaccharide-stimulated murine alveolar macrophages 80. Indirubin is an active ingredient of a TCM preparation Dang Gui Long Hui Pill, had strong antiviral and immunomodulatory effects, as shown by a study based on the observation of influenza H5N1 virus-infected human macrophages and type-I alveolar epithelial cells 81. Lian Hua Qing Wen Capsule was reported to have in vitro activity in inhibition of propagation of various influenza viruses. This TCM herbal product not only blocked the early stages of influenza virus infection but also inhibited virus-induced gene expression of IL-6, IL-8, TNF-a, IP-10, and MCP-1 82. Additionally, a study by Dong et al. reported that the levels of IL-8, TNF-α, IL-17, and IL-23 in the sputum and of IL-8 and IL-17 in the blood were markedly decreased after Lian Hua Qing Wen Capsule treatment in patients with acute exacerbation of chronic obstructive pulmonary disease 83. A self-control study by Poon et al. showed that the administration of the TCM herbal formulas (Sang Ju Yin and Yu Ping Feng San) may have beneficial immunomodulatory effects for the prevention of viral infections including SARS-CoV 46.

Moreover, a number of anti-coronaviral agents have been identified from TCM herbs, although the mechanisms of action have not yet been elucidated. For example, extracts from Lycoris radiata, Artemisia annua, Pyrrosia lingua, and Lindera aggregate possessed the anti-SARS‑CoV activity 84, 3β-Friedelanol isolated from Euphorbia neriifolia 85, Blancoxanthone isolated from the roots of Calophyllum blancoi 86 exhibited anti-HCoV-229E activity.

Traditional Chinese Medicine used in the treatment of SARS-CoV-2-infected patients: the current situations

TCM is highly valued by the government of China in their campaign to contain and eradiate SARS-CoV-2. For example, Health Commission in 26 provinces have officially declared that TCM should be used in combination with conventional medicine in the treatment of COVID-19 patients. On 17, February, National Health Commission (NHC) of the People's Republic of China reported that 60,107 confirmed COVID-19 patients (85.20% of total confirmed cases) had been treated with TCM 87. As for March 1, 2020, a total of 303 ongoing clinical trials aiming to evaluate the efficacy and safety of treatments for CoV-19 patients have been launched in China. Among them, 50 trials (16.5%) are about the use of TCM, including 14 cases (4.6%) to examine the effect of combined treatment with TCM and Western medicine. In 22 TCM trials (7.3%), the effect of self-made herbal preparations such as Xin Guan-1 Formula, Xin Guan-2 Formula and Qing Yi-4 are examined. In another 14 TCM trials (4.6%), commercially available TCM products such as Tan Re Qing Injection and Lian Hua Qing Wen Capsule are studied (Table 4).

Table 4.

Ongoing TCM Clinical Trials for the treatment of SARS-CoV-2 infection

Registration
number
Design type Title TCM herbal medicine Sample size Phase
ChiCTR2000029432 CCT A real world study for the efficacy and safety of large dose Tanreqing Injection in the treatment of patients with novel coronavirus pneumonia (COVID-19) Tan Re Qing Injection 72 4
ChiCTR2000029434 RCT A randomized, open-label, blank-controlled trial for Lian-Hua Qing-Wen Capsule/Granule in the treatment of novel coronavirus pneumonia (COVID-19) Lian Hua Qing Wen Capsule/Granule 400 4
ChiCTR2000029487 CCT Clinical study for Gu-Biao Jie-Du-Ling in preventing of novel coronavirus pneumonia (COVID-19) in children Gu Biao Jie Du Ling 200 0
ChiCTR2000029589 CCT An open, prospective, multicenter clinical study for the efficacy and safety of Reduning injection in the treatment of ovel coronavirus pneumonia (COVID-19) Re Du Ning
Injection
60 0
ChiCTR2000029605 RCT A randomized, open-label, blank-controlled, multicenter trial for Shuang-Huang-Lian oral solution in the treatment of novel coronavirus pneumonia (COVID-19) Shuang Huang Lian Oral Liquid 400 4
ChiCTR2000029780 RCT A multicenter, randomized, open, controlled trial for the efficacy and safety of Shen-Qi Fu-Zheng injection in the treatment of novel coronavirus pneumonia (COVID-19) Shen Qi Fu Zheng Injection 160 4
ChiCTR2000029781 RCT A multicenter, randomized, open and controlled trial for the efficacy and safety of Kang-Bing-Du granules in the treatment of novel coronavirus pneumonia (COVID-19) Kang Bing Du Granules 160 4
ChiCTR2000029822 RCT A randomized controlled trial for honeysuckle decoction in the treatment of patients with novel coronavirus (COVID-19) infection Jin Yin Hua Tang 110 0
ChiCTR2000029991 RCT A randomized, open-label, controlled trial for the safety and efficiency of Kesuting syrup and Keqing capsule in the treatment of mild and moderate novel coronavirus pneumonia (COVID-19) Ke Su Ting Syrup
/Ke Qing Capsule
72 4
ChiCTR2000030043 RCT Shen-Fu injection in the treatment of severe novel coronavirus pneumonia (COVID-19): a multicenter, randomized, open-label, controlled trial Shen Fu Injection 300 4
ChiCTR2000030117 RCT A multicenter, randomized, open, parallel controlled trial for the evaluation of the effectiveness and safety of Xiyanping injection in the treatment of common type novel coronavirus pneumonia (COVID-19) Xi Yan Ping Injection 348 4
ChiCTR2000030255 RCT Efficacy and safety of Jing-Yin Granule in the treatment of novel coronavirus pneumonia (COVID-19) wind-heat syndrome Jing Yin Granule 300 4
ChiCTR2000030388 RCT Efficacy and safety of Xue-Bi-Jing injection in the treatment of severe cases of novel coronavirus pneumonia (COVID-19) Xue Bi Jing Injection 60 0
ChiCTR2000029813 RCT Clinical Trial for Tanreqing Capsules in the Treatment of Novel Coronavirus Pneumonia (COVID-19) Tan Re Qing Capsules 72 0

Notes: RCT: randomized controlled trial; CCT: controlled clinical trial.

To date, NHC has published 6 editions Guidelines of Diagnosis and Treatment for COVID-19 88. Since the fourth versions, different herbal medicines used in TCM system has been recommended for the treatment of COVID-19, based on the stage of disease and symptom differentiation 89. According to the latest edition of Guideline 88, following multiple component Chinese herbal products are recommended for the patients in the medical observation period, presumably as a preventive measure: Huo Xiang Zheng Qi Shui, Lian Hua Qing Wen Capsule, Shu Feng Jie Du Capsule and Jin Hua Qing Gan Granule. In the clinical treatment period, Qing Fei Pai Du Tang, Xi Yan Ping Injection, Xue Bi Jing injection, Re Du Ning Injection, Tan Re Qing Injection, Xing Nao Jing Injection and some other Chinese medicine formulae should be selected 90. In addition, for the patients in critical condition, Shen Fu Injection, Sheng Mai Injection, Shen Mai Injection, Su He Xiang Pill and An Gong Niu Huang Pill should be administered (Table 5).

Table 5.

TCM recommended by 6th editions Guidelines of Diagnosis and Treatment for COVID-19 88.

Stage of disease Symptom Recommended Chinese patent medicine
Medical observation period Fatigue with gastrointestinal discomfort Huo Xiang Zheng Qi Shui
Fatigue with fever Lian Hua Qing Wen Capsule, Shu Feng Jie Du Capsule, Jin Hua Qing Gan Capsule
Clinical treatment period
(Confirmed patients)
Mild cases Qing Fei Pai Du Tang
General cases Qing Fei Pai Du Tang
Several cases Xi Yan Ping Injection, Xue Bi Jing Injection, Re Du Ning Injection, Tan Re Qing Injection, Xing Nao Jing Injection, Qing Fei Pai Du Tang
Critical cases Xue Bi Jing Injection, Re Du Ning Injection, Tan Re Qing Injection, Shen Fu Injection, Sheng Mai Injection, Shen Mai Injection, Su He Xiang Pill, An Gong Niu Huang Pill

Through analysis of the frequency of TCM used in 23 provinces, Luo, et al. 37 concluded that Astragalus membranaceus, Glycyrrhizae uralensis, Saposhnikoviae divaricata, Rhizoma Atractylodis Macrocephalae, Lonicerae Japonicae Flos, Fructus forsythia, Atractylodis Rhizoma, Radix platycodonis, Agastache rugosa, and Cyrtomium fortune J. Sm were 10 most commonly used Chinese herbs in the treatment of COVID-19. Xu, et al. 91 reported that Astragalus membranaceus and Yu Ping Feng were used in the 13 prevention programs (in Beijing, Tianjin, et al.) for “reinforcing vital qi”, a terminology used in TCM that is similar to boosting host defense capacity. Ophiopogon japonicas and Scrophularia ningpoensisand are TCM herbs which were most frequently used for “nourishing yin” in northern China, while Atractylodis Rhizoma, Agastache rugosa and other Chinese medicinal herbs with the property of “aromatic dehumidification” were commonly used in southern China (Table 6).

Table 6.

Frequently used TCM herbs for the Prevention of COVID-19 infection

Reported by Herbs (Latin name) Herbs (Chinese Pin Yin) Applicable regions
Luo, et al. 37 Astragalus membranaceus Huangqi 23 provinces covered Northeast, North, Central (including Wuhan), South, East, Northwest, and Southwest China.
Glycyrrhizae uralensis Gancao
Saposhnikoviae divaricata Fangfeng
Rhizoma Atractylodis Macrocephalae Baizhu
Lonicerae Japonicae Flos Jinyinhua
Fructus Forsythiae Lianqiao
Atractylodis Rhizoma Cangzhu
Radix platycodonis Jiegeng
Agastache rugosa Huoxiang
Cyrtomium fortune J. Sm Guanzhong
Xu, et al.91 Astragalus membranaceus Huangqi Beijing, Tianjin, Shandong, Shaanxi, Gansu, Hebei, Shanxi, Henan, Hubei, Jiangxi, Hunan, and Yunnan
Atractylodis Rhizoma Cangzhu Five regions in southern China (Hubei, Jiangxi, Hunan, Yunnan, and Wuhan)
Eupatorii Herba Peilan
Agastache rugosa Huoxiang
Ophiopogon japonicas Maidong Eight regions in northern China (Beijing, Tianjin, Hebei, Henan, Shaanxi, Shanxi, Gansu, and Shandong)
Scrophularia ningpoensis Xuanshen
Rhizoma phragmitis Lugen
Adeinophora stricta Miq Shashen
Dendrobium nobile Lindl. Shihu

According to the report of National Administration of Traditional Chinese Medicine, up to February 5th, 2020, 214 COVID-19 patients were treated with Qing Fei Pai Du Tang in Shanxi, Hebei, Heilongjiang and Shaanxi Provinces with overall effective rate ≥ 90%. Among them, the symptoms of majority of patients (≥60%) were markedly improved, while illness of others (30%) was stabilized 92. After that, 701 COVID-19 patients were treated with Qing Fei Pai Du Tang in 10 provinces in China. The result showed that 130 patients (18.5%) were completely cured after treatment. The treatment also resulted in the disappearance of characteristic symptoms of COVID-19 such as fever and cough in 51 patients (7.27%). In addition, symptom improvement or stabilization were observed in 268 patients (38.2%), and in 212 patients (30.2%), respectively 87. Yao, et al. and Lu, et al. 93, 94 retrospectively analyzed the clinical efficacy of Lian Hua Qing Wen Capsule in treatment of confirmed and suspected COVID-19 patients. The results indicated that this herbal product could markedly relieve major symptoms such as fever and cough and had the capacity to promote the recovery.

Some patients with mild illness in the early stage could suddenly progress to severe disease, and eventually died due to septic shock with multiple organ dysfunction syndrome (MODS), which was associated with cytokine storm 95. There is compelling evidence that some TCM herbal products or its components have potent immunosuppressive effects, as shown by our own and other's studies 79, 96-103. For example, Wang, et al. 104 reported that Shen Fu Injection could inhibit the lung inflammation and decrease the levels of IL-1β, IL-6 and other cytokines. Chang, et al. 105 reported that Re Du Ning Injection could markedly reduce the levels of IL-1β, TNF-α, IL-8, IL-10, and some other cytokines of LPS-induced model of acute lung injury in rats. We recently reported that tetrandrine, a compound isolated from an anti-rheumatic Chinese herb, could potently inhibit proinflammatory Th1, Th2 and Th17 responses in LPS-challenged mice 106. Therefore, TCM with the capacity to inhibit cytokine storm and its devastating consequences may be harnessed in the treatment of severe COVID-19 patients.

Currently, the laboratory study on the effect of TCM is apparently lagging behind the clinical application of TCM in the treatment of COVID-19 patients. Nevertheless, some scientists have started to examine the effect of TCM products or its components on SARS-CoV-2 in their laboratories. For example, an in vitro study showed that Shuang Huang Lian Oral Liquid had the inhibitory effect on SARS-CoV-2 78. However, its clinical efficacy and safety for the treatment of COVID-19 patients has not been evaluated. We noticed that this TCM product was not recommended by HNC's Guideline 89. Same as SARS-CoV, SARS-CoV-2 uses receptor ACE2 for the cellular entrance 8. Theoretically, blockade of ACE2 can prevent the infection of SARS-CoV-2. Chen and Du thus performed the molecular docking study and they found that TCM-derived compounds, including as baicalin, scutellarin, hesperetin, glycyrrhizin and nicotianamine could interact with ACE2 107. Therefore, these compounds as well as herbs containing these ingredients may have the capacity to inhibit the infection of SARS-CoV-2. We anticipate more experiment studies showing anti-SARS-CoV-2 activity of TCM or its components will be published in the near future.

Closing remarks

TCM has accumulated thousand-of-year's experiences in the treatment of pandemic and endemic diseases. Providing complementary and alternative treatments are still urgently needed for the management of patients with SARS-CoV-2 infection, experiences in TCM is certainly worth learning. Fighting against current epidemics also provide an opportunity to test the true value of TCM in treating emerging contagious diseases. Randomized, double-blind and placebo-controlled studies is the best way to provide the most reliable evidence for a therapy, including TCM. It is encouraging that the controlled clinical studies to evaluate the efficacy of TCM in the treatment of SARS-CoV were conducted and reported. However, the most of these studies were found to be poorly designed and the results could lead to potential biases in evaluating the effectiveness of TCM treatment 13. Hopefully, current clinical study to evaluate the effect of TCM on COVID-19 will use more strict protocols, concealment of allocation, and double-blinding, in order to ensure the compliance of international acceptable standards. Furthermore, standardized products of TCM, rather than self-prepared formulations, should be used in clinical study. Experiment study may be able to elucidate the mechanism underlying the therapeutic effect of TCM in the treatment of COVID-19. The further study of TCM may lead to the identification of novel anti human coronavirus compounds that may eventually prove to be useful in the treatment of SARS-CoV-2 or other emerging fatal viral diseases as conventional therapeutic agents.

The safety of TCM in the treatment of emerging coronavirus diseases was not included in the observation on SARS patients 13. It was reported that some herbs used in TCM contain nephrotoxins and mutagens 108, while the toxicological features of the most of Chinese herbal medicines remain to be fully understood 109. Furthermore, herbs used in TCM can mimic, or magnify, or oppose the effect of conventional medicines 110. Thus, the safety of TCM used in treatment of emerging coronavirus infections should be carefully evaluated. It is particularly important to avoid toxicity or interfere with the efficacy of conventional treatment caused by herb-drug interaction.

Supplementary Material

Supplementary figures and tables.

Acknowledgments

This project has been funded by Macau Science and Technology Development Fund (FDCT) research grant 201/2017/A3 and 0056/2019/AFJ and University of Macau research grant MYRG2017-00120- ICMS and MYRG2019-00169-ICMS.

References

  • 1.Gralinski LE, Menachery VD. Return of the Coronavirus: 2019-nCoV. Viruses. 2020. 12. [DOI] [PMC free article] [PubMed]
  • 2.Burki TK. Coronavirus in China. Lancet Respir Med. 2020. [DOI] [PMC free article] [PubMed]
  • 3.World Health Organization. WHO Director-General's remarks at the media briefing on 2019-nCoV on 11 February 2020. https://www.who.int/dg/speeches/detail/who-director-general-s-remarks-at-the-media-briefing-on-2019-ncov-on-11-february-2020. 2020.
  • 4.Guan WJ, Ni ZY, Hu Y, Liang WH, Ou CQ, He JX, Clinical characteristics of 2019 novel coronavirus infection in China. medRxiv. 2020. 2020. 02.06.20020974.
  • 5.Huang C, Wang Y, Li X, Ren L, Zhao J, Hu Y. et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 2020;395(10223):497–506. doi: 10.1016/S0140-6736(20)30183-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.World Health Organization. Situation Report-29. https://www.who.int/docs/default-source/coronaviruse/situation-reports/20200218-sitrep-29-covid-19.pdf?sfvrsn=6262de9e_2. 2020.
  • 7.Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y. et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020;395(10223):507–513. doi: 10.1016/S0140-6736(20)30211-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Zhou P, Yang XL, Wang XG, Hu B, Zhang L, Zhang W, A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020. [DOI] [PMC free article] [PubMed]
  • 9.Wu A, Peng Y, Huang B, Ding X, Wang X, Niu P, Genome Composition and Divergence of the Novel Coronavirus (2019-nCoV) Originating in China. Cell Host Microbe. 2020. [DOI] [PMC free article] [PubMed]
  • 10.Zumla A, Chan JF, Azhar EI, Hui DS, Yuen KY. Coronaviruses - drug discovery and therapeutic options. Nat Rev Drug Discov. 2016;15:327–47. doi: 10.1038/nrd.2015.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Xie X, Zhong Z, Zhao W, Zheng C, Wang F, Liu J. Chest CT for Typical 2019-nCoV Pneumonia: Relationship to Negative RT-PCR Testing. Radiology. 2020: 200343. [DOI] [PMC free article] [PubMed]
  • 12.Li G, Clercq ED. Therapeutic options for the 2019 novel coronavirus (2019-nCoV) Nat Rev Drug Discov. 2020. [DOI] [PubMed]
  • 13.Liu J, Manheimer E, Shi Y, Gluud C. Chinese herbal medicine for severe acute respiratory syndrome: a systematic review and meta-analysis. J Altern Complement Med. 2004;10:1041–51. doi: 10.1089/acm.2004.10.1041. [DOI] [PubMed] [Google Scholar]
  • 14.Li T, Peng T. Traditional Chinese herbal medicine as a source of molecules with antiviral activity. Antiviral Res. 2013;97:1–9. doi: 10.1016/j.antiviral.2012.10.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Leung PC. The efficacy of Chinese medicine for SARS: a review of Chinese publications after the crisis. Am J Chin Med. 2007;35:575–81. doi: 10.1142/S0192415X07005077. [DOI] [PubMed] [Google Scholar]
  • 16.Jin YH, Cai L, Cheng ZS, Cheng H, Deng T, Fan YP. et al. A rapid advice guideline for the diagnosis and treatment of 2019 novel coronavirus (2019-nCoV) infected pneumonia (standard version) Mil Med Res. 2020;7:4. doi: 10.1186/s40779-020-0233-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Habibzadeh P, Stoneman EK. The Novel Coronavirus: A Bird's Eye View. Int J Occup Environ Med. 2020;11:65–71. doi: 10.15171/ijoem.2020.1921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Jordan PC, Stevens SK, Deval J. Nucleosides for the treatment of respiratory RNA virus infections. Antivir Chem Chemother. 2018;26:2040206618764483. doi: 10.1177/2040206618764483. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.De Clercq E. New Nucleoside Analogues for the Treatment of Hemorrhagic Fever Virus Infections. Chem Asian J. 2019;14:3962–8. doi: 10.1002/asia.201900841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Wang M, Cao R, Zhang L, Yang X, Liu J, Xu M, Remdesivir and chloroquine effectively inhibit the recently emerged novel coronavirus (2019-nCoV) in vitro. Cell Res. 2020. [DOI] [PMC free article] [PubMed]
  • 21.Sheahan TP, Sims AC, Graham RL, Menachery VD, Gralinski LE, Case JB, Broad-spectrum antiviral GS-5734 inhibits both epidemic and zoonotic coronaviruses. Sci Transl Med. 2017. 9. [DOI] [PMC free article] [PubMed]
  • 22.Zhang L, Liu Y. Potential Interventions for Novel Coronavirus in China: A Systemic Review. J Med Virol. 2020. [DOI] [PMC free article] [PubMed]
  • 23.Holshue ML, DeBolt C, Lindquist S, Lofy KH, Wiesman J, Bruce H, First Case of 2019 Novel Coronavirus in the United States. N Engl J Med. 2020. [DOI] [PMC free article] [PubMed]
  • 24.Lai CC, Shih TP, Ko WC, Tang HJ, Hsueh PR. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and corona virus disease-2019 (COVID-19): the epidemic and the challenges. Int J Antimicrob Agents. 2020: 105924. [DOI] [PMC free article] [PubMed]
  • 25.Savarino A, Di Trani L, Donatelli I, Cauda R, Cassone A. New insights into the antiviral effects of chloroquine. Lancet Infect Dis. 2006;6:67–9. doi: 10.1016/S1473-3099(06)70361-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Yan Y, Zou Z, Sun Y, Li X, Xu KF, Wei Y. et al. Anti-malaria drug chloroquine is highly effective in treating avian influenza A H5N1 virus infection in an animal model. Cell Res. 2013;23:300–2. doi: 10.1038/cr.2012.165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Wong CK, Lam CW, Wu AK, Ip WK, Lee NL, Chan IH. et al. Plasma inflammatory cytokines and chemokines in severe acute respiratory syndrome. Clin Exp Immuno. 2004;136:95–103. doi: 10.1111/j.1365-2249.2004.02415.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.He L, Ding Y, Zhang Q, Che X, He Y, Shen H. et al. Expression of elevated levels of pro-inflammatory cytokines in SARS-CoV-infected ACE2+ cells in SARS patients: relation to the acute lung injury and pathogenesis of SARS. J Pathol. 2006;210:288–97. doi: 10.1002/path.2067. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Faure E, Poissy J, Goffard A, Fournier C, Kipnis E, Titecat M. et al. Distinct immune response in two MERS-CoV-infected patients: can we go from bench to bedside? PLoS One. 2014;9:e88716. doi: 10.1371/journal.pone.0088716. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Falzarano D, de Wit E, Rasmussen AL, Feldmann F, Okumura A, Scott DP. et al. Treatment with interferon-alpha2b and ribavirin improves outcome in MERS-CoV-infected rhesus macaques. Nat Med. 2013;19:1313–7. doi: 10.1038/nm.3362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Stockman LJ, Bellamy R, Garner P. SARS: systematic review of treatment effects. PLoS Med. 2006;3:e343. doi: 10.1371/journal.pmed.0030343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Lansbury L, Rodrigo C, Leonardi-Bee J, Nguyen-Van-Tam J, Lim WS. Corticosteroids as adjunctive therapy in the treatment of influenza. Cochrane Database Syst Rev. 2019;2:Cd010406. doi: 10.1002/14651858.CD010406.pub3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Arabi YM, Mandourah Y, Al-Hameed F, Sindi AA, Almekhlafi GA, Hussein MA. et al. Corticosteroid Therapy for Critically Ill Patients with Middle East Respiratory Syndrome. Am J Respir Crit Care Med. 2018;197:757–67. doi: 10.1164/rccm.201706-1172OC. [DOI] [PubMed] [Google Scholar]
  • 34.Russell CD, Millar JE, Baillie JK. Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury. Lancet. 2020. [DOI] [PMC free article] [PubMed]
  • 35. World Health Organization. https://www.who.int/internal-publications-detail/clinical-management-of-severe-acute-respiratory-infection-when-novel-coronavirus-(ncov)-infection-is-suspected. 2020.
  • 36.Hung IFN, To KKW, Lee CK, Lee KL, Yan WW, Chan K. et al. Hyperimmune IV immunoglobulin treatment: a multicenter double-blind randomized controlled trial for patients with severe 2009 influenza A(H1N1) infection. Chest. 2013;144:464–73. doi: 10.1378/chest.12-2907. [DOI] [PubMed] [Google Scholar]
  • 37.Luo H, Tang QL, Shang YX, Liang SB, Yang M, Robinson N, Can Chinese Medicine Be Used for Prevention of Corona Virus Disease 2019 (COVID-19)? A Review of Historical Classics, Research Evidence and Current Prevention Programs. Chin J Integr Med. 2020. [DOI] [PMC free article] [PubMed]
  • 38.Tong X, Li A, Zhang Z, Duan J, Chen X, Hua C. et al. TCM treatment of infectious atypical pneumonia-a report of 16 cases. J Tradit Chin Med. 2004;24:266–9. [PubMed] [Google Scholar]
  • 39.Liu X, Zhang M, He L, Li Y. Chinese herbs combined with Western medicine for severe acute respiratory syndrome (SARS) Cochrane Database Syst Rev. 2012;10:Cd004882. doi: 10.1002/14651858.CD004882.pub3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Zhang MM, Liu XM, He L. Effect of integrated traditional Chinese and Western medicine on SARS: a review of clinical evidence. World J Gastroenterol. 2004;10:3500–5. doi: 10.3748/wjg.v10.i23.3500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Zhong N, May RM, McLean AR, Pattison J, Weiss RA. Management and prevention of SARS in China. Philos Trans R Soc Lond B Biol Sci. 2004;359:1115–6. doi: 10.1098/rstb.2004.1491. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.JSM P, D P, Yuen KY ea. The Severe Acute Respiratory Syndrome. New Engl J Med. 2003;249:2431–41. doi: 10.1056/NEJMra032498. [DOI] [PubMed] [Google Scholar]
  • 43.Jr TMF, Tsang KWT. Severe Acute Respiratory Syndrome. Nat Med. 2005;4:95–106. doi: 10.2165/00151829-200504020-00003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Chen Z, Nakamura T. Statistical evidence for the usefulness of Chinese medicine in the treatment of SARS. Phytotherapy research: PTR. 2004;18:592–4. doi: 10.1002/ptr.1485. [DOI] [PubMed] [Google Scholar]
  • 45.T.F. Lau, Leung PC, Wong ELY, Fong C, Cheng KF, Zhang SC, et al. Using Herbal Medicine as a Means of Prevention Experience During the SARS Crisis. Am J Chin Med. 2005;33:345–56. doi: 10.1142/S0192415X05002965. [DOI] [PubMed] [Google Scholar]
  • 46.Poon PM, Wong CK, Fung KP, Fong CY, Wong EL, Lau JT. et al. Immunomodulatory effects of a traditional Chinese medicine with potential antiviral activity: a self-control study. Am J Chin Med. 2006;34:13–21. doi: 10.1142/S0192415X0600359X. [DOI] [PubMed] [Google Scholar]
  • 47.Hsu CH, Hwang KC, Chao CL, Chang SG, Ho MS, Chou P. Can herbal medicine assist against avian flu? Learning from the experience of using supplementary treatment with Chinese medicine on SARS or SARS-like infectious disease in 2003. J Altern Complement Med. 2006;12:505–6. doi: 10.1089/acm.2006.12.505. [DOI] [PubMed] [Google Scholar]
  • 48.Cinatl J, Morgenstern B, Bauer G, Chandra P, Rabenau H, Doerr HW. Glycyrrhizin, an active component of liquorice roots, and replication of SARS-associated coronavirus. The Lancet. 2003;361:2045–6. doi: 10.1016/S0140-6736(03)13615-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Chen F, Chan KH, Jiang Y, Kao RY, Lu HT, Fan KW. et al. In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds. J Clin Virol. 2004;31:69–75. doi: 10.1016/j.jcv.2004.03.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Wang SQ, Du QS, Zhao K, Li AX, Wei DQ, Chou KC. Virtual screening for finding natural inhibitor against cathepsin-L for SARS therapy. Amino Acids. 2007;33:129–35. doi: 10.1007/s00726-006-0403-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Wu T, Yang X, Zeng X, Poole P. Traditional Chinese medicine in the treatment of acute respiratory tract infections. Resp Med. 2008;102:1093–8. doi: 10.1016/j.rmed.2008.03.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Cragg GM, Newman DJ. Natural products: a continuing source of novel drug leads. Biochimica et biophysica acta. 2013;1830:3670–95. doi: 10.1016/j.bbagen.2013.02.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Luo W, Su X, Gong S, Qin Y, Liu W, Li J, Anti-SARS coronavirus 3C-like protease effects of Rheum palmatum L. extracts. BioScience Trends. 2009. 3. [PubMed]
  • 54.Fung KP, Leung PC, Tsui KW, Wan CC, Wong KB, Waye MY. et al. Immunomodulatory activities of the herbal formula Kwan Du Bu Fei Dang in healthy subjects: a randomised, double-blind, placebo-controlled study. Hong Kong Med J. 2011;17(Suppl 2):41–3. [PubMed] [Google Scholar]
  • 55.Lau KM, Lee KM, Koon CM, Cheung CS, Lau CP, Ho HM. et al. Immunomodulatory and anti-SARS activities of Houttuynia cordata. J Ethnopharmacol. 2008;118:79–85. doi: 10.1016/j.jep.2008.03.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Gong SJ, Su XJ, Yu HP, Li J, Qin YJ, Xu Q. et al. A study on anti-SARS-CoV 3CL protein of flavonoids from litchi chinensis sonn core. Chinese Pharmacological Bulletin. 2008;24:699–700. [Google Scholar]
  • 57.Lin CW, Tsai FJ, Tsai CH, Lai CC, Wan L, Ho TY. et al. Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds. Antiviral Res. 2005;68:36–42. doi: 10.1016/j.antiviral.2005.07.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Nguyen TTH, Woo HJ, Kang HK, Nguyen VD, Kim YM, Kim DW. et al. Flavonoid-mediated inhibition of SARS coronavirus 3C-like protease expressed in Pichia pastoris. Biotechnol Lett. 2012;34:831–8. doi: 10.1007/s10529-011-0845-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Jo S, Kim S, Shin DH, Kim M-S. Inhibition of SARS-CoV 3CL protease by flavonoids. J Enzyme Inhib Med Chem. 2020;35:145–51. doi: 10.1080/14756366.2019.1690480. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.Jo S, Kim H, Kim S, Shin DH, Kim MS. Characteristics of flavonoids as potent MERS-CoV 3C-like protease inhibitors. Chem Biol Drug Des. 2019. [DOI] [PMC free article] [PubMed]
  • 61.Yu MS, Lee J, Lee JM, Kim Y, Chin YW, Jee JG. et al. Identification of myricetin and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13. Bioorg Med Chem Lett. 2012;22:4049–54. doi: 10.1016/j.bmcl.2012.04.081. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Wu CY, Jan JT, Ma SH, Kuo CJ, Juan HF, Cheng YSE. et al. Small molecules targeting severe acute respiratory syndrome human coronavirus. Proc Natl Acad Sci U S A. 2004;101:10012–7. doi: 10.1073/pnas.0403596101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63.Kuhn JH, Radoshitzky SR, Li W, Wong SK, Choe H, Farzan M. The SARS Coronavirus receptor ACE 2 A potential target for antiviral therapy. In: Holzenburg A, Bogner E, editors. New Concepts of Antiviral Therapy. Boston, MA: Springer US. 2006. p. 397-418.
  • 64.Letko M, Munster V. Functional assessment of cell entry and receptor usage for lineage B β-coronaviruses, including 2019-nCoV. bioRxiv. 2020. 2020. 01.22.915660. [DOI] [PMC free article] [PubMed]
  • 65.Lin HX, Feng Y, Wong G, Wang L, Li B, Zhao X. et al. Identification of residues in the receptor-binding domain (RBD) of the spike protein of human coronavirus NL63 that are critical for the RBD-ACE2 receptor interaction. J Gen Virol. 2008;89:1015–24. doi: 10.1099/vir.0.83331-0. [DOI] [PubMed] [Google Scholar]
  • 66.Xu XT, Chen P, Wang JF, Feng JN, Zhou H, Li X, Evolution of the novel coronavirus from the ongoing Wuhan outbreak and modeling of its spike protein for risk of human transmission. Sci China Life Sci. 2020. [DOI] [PMC free article] [PubMed]
  • 67.Ho T, Wu S, Chen J, Li C, Hsiang C. Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction. Antiviral Res. 2007;74:92–101. doi: 10.1016/j.antiviral.2006.04.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Deng YF, Aluko RE, Jin Q, Zhang Y, Yuan LJ. Inhibitory activities of baicalin against renin and angiotensin-converting enzyme. Pharm Biol. 2012;50:401–6. doi: 10.3109/13880209.2011.608076. [DOI] [PubMed] [Google Scholar]
  • 69.Takahashi S, Yoshiya T, Yoshizawa-Kumagaye K, Sugiyama T. Nicotianamine is a novel angiotensin-converting enzyme 2 inhibitor in soybean. Biomed Res. 2015;36:219–24. doi: 10.2220/biomedres.36.219. [DOI] [PubMed] [Google Scholar]
  • 70.Wang W, Ma X, Han J, Zhou M, Ren H, Pan Q. et al. Neuroprotective Effect of Scutellarin on Ischemic Cerebral Injury by Down-Regulating the Expression of Angiotensin-Converting Enzyme and AT1 Receptor. PLoS One. 2016;11:e0146197. doi: 10.1371/journal.pone.0146197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Yi L, Li Z, Yuan K, Qu X, Chen J, Wang G. et al. Small molecules blocking the entry of severe acute respiratory syndrome coronavirus into host cells. J Virol. 2004;78:11334–9. doi: 10.1128/JVI.78.20.11334-11339.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Schwarz S, Wang K, Yu WJ, Sun B, Schwarz W. Emodin inhibits current through SARS-associated coronavirus 3a protein. Antiviral res. 2011;90:64–9. doi: 10.1016/j.antiviral.2011.02.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Schwarz S, Sauter D, Wang K, Zhang R, Sun B, Karioti A. et al. Kaempferol Derivatives as Antiviral Drugs against the 3a Channel Protein of Coronavirus. Planta Medica. 2014;80:177–82. doi: 10.1055/s-0033-1360277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Cheng PW, Ng LT, Chiang LC, Lin CC. Antiviral effects of saikosaponins on human coronavirus 229E in vitro. Clin Exp Pharmacol Physiol. 2006;33:612–6. doi: 10.1111/j.1440-1681.2006.04415.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Pilcher H. Liquorice may tackle SARS. Nature. 2003.
  • 76.Chen CJ, Michaelis M, Hsu HK, Tsai CC, Yang KD, Wu YC. et al. Toona sinensis Roem tender leaf extract inhibits SARS coronavirus replication. J Ethnopharmacol. 2008;120:108–11. doi: 10.1016/j.jep.2008.07.048. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Lu H. Drug treatment options for the 2019-new coronavirus (2019-nCoV) Biosci Trends. 2020. [DOI] [PubMed]
  • 78. Science CAo. Researchers in Shanghai Institute of Drugs and Wuhan Virus Institute discovered that the Chinese patent medicine Shuanghuanglian oral liquid can inhibit the 2019-new coronavirus.; 2020.
  • 79.Chen X, Howard OM, Yang X, Wang L, Oppenheim JJ, Krakauer T. Effects of Shuanghuanglian and Qingkailing, two multi-components of traditional Chinese medicinal preparations, on human leukocyte function. Life Sci. 2002;70:2897–913. doi: 10.1016/s0024-3205(02)01541-2. [DOI] [PubMed] [Google Scholar]
  • 80.Gao Y, Fang L, Cai R, Zong C, Chen X, Lu J. et al. Shuang-Huang-Lian exerts anti-inflammatory and anti-oxidative activities in lipopolysaccharide-stimulated murine alveolar macrophages. Phytomedicine. 2014;21:461–9. doi: 10.1016/j.phymed.2013.09.022. [DOI] [PubMed] [Google Scholar]
  • 81.Chan MC, Chan RW, Mok CK, Mak NK, Wong RN. Indirubin-3'-oxime as an antiviral and immunomodulatory agent in treatment of severe human influenza virus infection. Hong Kong Med J. 2018;24(Suppl 6):45–7. [PubMed] [Google Scholar]
  • 82.Ding Y, Zeng L, Li R, Chen Q, Zhou B, Chen Q. et al. The Chinese prescription lianhuaqingwen capsule exerts anti-influenza activity through the inhibition of viral propagation and impacts immune function. BMC Complement Altern Med. 2017;17:130. doi: 10.1186/s12906-017-1585-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Dong L, Xia JW, Gong Y, Chen Z, Yang H-H, Zhang J. et al. Effect of Lianhuaqingwen Capsules on Airway Inflammation in Patients with Acute Exacerbation of Chronic Obstructive Pulmonary Disease. Evid Based Complement Alternat Med. 2014;2014:1–11. doi: 10.1155/2014/637969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Li S, Chen C, Zhang H, Guo H, Wang H, Wang L. et al. Identification of natural compounds with antiviral activities against SARS-associated coronavirus. Antiviral Res. 2005;67:18–23. doi: 10.1016/j.antiviral.2005.02.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Chang FR, Yen CT, Ei-Shazly M, Lin WH, Yen MH, Lin KH. et al. Anti-Human Coronavirus (anti-HCoV) Triterpenoids from the Leaves of Euphorbia Neriifolia. Nat Prod Commun. 2012;7:1934578X1200701103. [PubMed] [Google Scholar]
  • 86.Shen YC, Wang LT, Khalil AT, Chiang LC, Cheng PW. Bioactive Pyranoxanthones from the Roots of Calophyllum blancoi. Chem Pharm Bull. 2005;53:244–7. doi: 10.1248/cpb.53.244. [DOI] [PubMed] [Google Scholar]
  • 87.National Health Commission of the People's Republic of China. Transcript of press conference in 17, February, 2020. http://www.nhc.gov.cn/xcs/s3574/202002/f12a62d10c2a48c6895cedf2faea6e1f. shtml. 2020.
  • 88.National Health Commission of the People's Republic of China. Notice on the issunance of guidelines of diagnosis and treatment for 2019-nCoV infected pneumonia (version 6) 6 ed; http://www.nhc.gov.cn/yzygj/s7653p/202002/8334a8326dd94d329df351d7da8aefc2.shtml?from=timeline. 2020.
  • 89.Han YY, Zhao MR, Shi B, Song ZH, Zhou SP, He Y. Application of integrative medicine protocols on treatment of coronavirus disease 2019. Chi Tradit Herbal Drugs. 1-5.
  • 90.Zhu YG, Deng ZW, Liu LH, Liu XH, Li XZ, Chen WH, Compilation of drug information for the diagnosis and treatment of COVID-19 (version 1) Central South Pharmacy. 1-14.
  • 91.Xu X, Zhang Y, Li X, Li XX. Analysis on prevention plan of corona virus disease-19 (COVID-19) by traditional Chinese medicine in various regions. Chin Herb Med. 2020. pp. 1–7.
  • 92.Zhao J, Tian SS, Yang J, Liu J, Zhang WD. Investigating the mechanism of Qing-Fei-Pai-Du-Tang for the treatment of Novel Coronavirus Pneumonia by network pharmacology. Chin Herb Med. 2020. pp. 1–7.
  • 93.Yao KT, Liu MY, Li X, Huang JH, Cai HB. Retrospective Clinical Analysis on Treatment of Novel Coronavirus-infected Pneumonia with Traditional Chinese Medicine Lianhua Qingwen. Chin J Exp Tradit Med Form. 2020. pp. 1–7.
  • 94.Lv RB, Wang WJ, Li X. Treatment of suspected new coronavirus pneumonia with Chinese medicine Lianhua Qingwen Clinical observation of 63 suspected cases. J Tradit Chin Med. 2020. pp. 1–5.
  • 95.Zhang JW, Hu X, Jin PF. Cytokine storms caused by 2019-nCoV and drug therapy. Chinese Pharmaceutical Journal. 2020. pp. 1–9. 96.
  • 96.Chen X, Yang D, Shen W, Dong HF, Wang JM, Oppenheim JJ. et al. Characterization of chenodeoxycholic acid as an endogenous antagonist of the G-coupled formyl peptide receptors. Inflamm Res. 2000;49:744–55. doi: 10.1007/s000110050656. [DOI] [PubMed] [Google Scholar]
  • 97.Chen X, Mellon RD, Yang L, Dong H, Oppenheim JJ, Howard OM. Regulatory effects of deoxycholic acid, a component of the anti-inflammatory traditional Chinese medicine Niuhuang, on human leukocyte response to chemoattractants. Biochem Pharmacol. 2002;63:533–41. doi: 10.1016/s0006-2952(01)00917-0. [DOI] [PubMed] [Google Scholar]
  • 98.Chen X, Beutler JA, McCloud TG, Loehfelm A, Yang L, Dong HF. et al. Tannic acid is an inhibitor of CXCL12 (SDF-1alpha)/CXCR4 with antiangiogenic activity. Clin Cancer Res. 2003;9:3115–23. [PubMed] [Google Scholar]
  • 99.Chen X, Yang L, Zhang N, Turpin JA, Buckheit RW, Osterling C. et al. Shikonin, a component of chinese herbal medicine, inhibits chemokine receptor function and suppresses human immunodeficiency virus type 1. Antimicrob Agents Chemother. 2003;47:2810–6. doi: 10.1128/AAC.47.9.2810-2816.2003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Chen X, Oppenheim JJ, Howard OM. Chemokines and chemokine receptors as novel therapeutic targets in rheumatoid arthritis (RA): inhibitory effects of traditional Chinese medicinal components. Cell Mol Immunol. 2004;1:336–42. [PubMed] [Google Scholar]
  • 101.Chen X, Murakami T, Oppenheim JJ, Howard OM. Triptolide, a constituent of immunosuppressive Chinese herbal medicine, is a potent suppressor of dendritic-cell maturation and trafficking. Blood. 2005;106:2409–16. doi: 10.1182/blood-2005-03-0854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.He J, He ZD, Chen X. Effects of Chinese medicinal components on chemokine receptors: theory, results and methodology. Evidence-based Research Methods for Chinese Medicine. 2016. pp. 187–97.
  • 103.Chen YB, Chen X. Ancient herbal component may be a novel therapeutic for gouty arthritis. J Leukoc Biol. 2019;105:7–9. doi: 10.1002/JLB.3CE1018-384R. [DOI] [PubMed] [Google Scholar]
  • 104.Wang J, Qiao LF, Li YS, Yang GT. Shen Fu injection activate the macrophage NF-kB of rats' alveolar induced by LPS. Acta Medicinae Universitatis Scientiae et Technologiae Huazhong. 2009;1:15–8. [Google Scholar]
  • 105.Chang XJ, Xiao W, Zhang S, Chang YP, Chen CM, Chen J. et al. Mechanism of Re Du Ning injection on anti-acute lung injury in rats based on cytokines storm. Chin Herb Med. 2014;46:236–9. [Google Scholar]
  • 106.Zou HM, He TZ, Chen X. Tetrandrine inhibits differentiation of proinflammatory subsets of T helper cells but spares de novo differentiation of iTreg cells. Int Immunopharmacol. 2019;69:307–12. doi: 10.1016/j.intimp.2019.01.040. [DOI] [PubMed] [Google Scholar]
  • 107.Chen H, Du Q. Potential Natural Compounds for Preventing 2019-nCoV Infection. Preprints. 2020.
  • 108.Ng AWT, Poon SL, Huang MN, Lim JQ, Boot A, Yu W, Aristolochic acids and their derivatives are widely implicated in liver cancers in Taiwan and throughout Asia. Sci Trans Med. 2017. 9. [DOI] [PubMed]
  • 109.Zeng ZP, Jiang JG. Analysis of the adverse reactions induced by natural product-derived drugs. Br J Pharmacol. 2010;159:1374–91. doi: 10.1111/j.1476-5381.2010.00645.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Fugh-Berman A. Herb-drug interactions. Lancet. 2000;355:134–8. doi: 10.1016/S0140-6736(99)06457-0. [DOI] [PubMed] [Google Scholar]
  • 111.Liu LS, Lei N, Lin Q, Wang WL, Yan HW, Duan XH. The Effects and Mechanism of Yinqiao Powder on Upper Respiratory Tract Infection. Int J Biotechnol Wellness Ind. 2015;4:57–60. [Google Scholar]
  • 112.Fu YJ, Yan YQ, Qin HQ, Wu S, Shi SS, Zheng X. et al. Effects of different principles of Traditional Chinese Medicine treatment on TLR7/NF-κB signaling pathway in influenza virus infected mice. Chin Med. 2018;13:42. doi: 10.1186/s13020-018-0199-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 113.Lau JT, Leung PC, Wong EL, Fong C, Cheng KF, Zhang SC. et al. The use of an herbal formula by hospital care workers during the severe acute respiratory syndrome epidemic in Hong Kong to prevent severe acute respiratory syndrome transmission, relieve influenza-related symptoms, and improve quality of life: a prospective cohort study. J Altern Complement Med. 2005;11:49–55. doi: 10.1089/acm.2005.11.49. [DOI] [PubMed] [Google Scholar]
  • 114.Du CY, Zheng KY, Bi CW, Dong TT, Lin H, Tsim KW. Yu Ping Feng San, an Ancient Chinese Herbal Decoction, Induces Gene Expression of Anti-viral Proteins and Inhibits Neuraminidase Activity. Phytother Res. 2015;29:656–61. doi: 10.1002/ptr.5290. [DOI] [PubMed] [Google Scholar]
  • 115.Gao J, Li J, Shao X, Jin Y, Lu XW, Ge JF. et al. Antiinflammatory and immunoregulatory effects of total glucosides of Yupingfeng powder. Chin Med J (Engl) 2009;122:1636–41. [PubMed] [Google Scholar]
  • 116.Zhang H, Chen Q, Zhou W, Gao S, Lin H, Ye S. et al. Chinese medicine injection shuanghuanglian for treatment of acute upper respiratory tract infection: a systematic review of randomized controlled trials. Evid Based Complement Alternat Med. 2013;2013:987326. doi: 10.1155/2013/987326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Xiao GL, Song K, Yuan CJ ea. A literature report on the treatment of SARS by stages with traditional Chinese medicine. J Emerg Chin Med Hunan. 2005. pp. 53–5.
  • 118.Bao L, J M. Research progress of Da Yuan Yin on the treatment of infectious diseases. Emerg Tradit Chin Med. 2010;2:263–87. [Google Scholar]
  • 119.Kim DE, Min JS, Jang MS, Lee JY, Shin YS, Song JH. et al. Natural Bis-Benzylisoquinoline Alkaloids-Tetrandrine, Fangchinoline, and Cepharanthine, Inhibit Human Coronavirus OC43 Infection of MRC-5 Human Lung Cells. Biomolecules. 2019;9:696. doi: 10.3390/biom9110696. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary figures and tables.


Articles from International Journal of Biological Sciences are provided here courtesy of Ivyspring International Publisher

RESOURCES