Sepsis-induced immunoparalysis: mechanisms, markers, and treatment options
- PMID: 24878876
Sepsis-induced immunoparalysis: mechanisms, markers, and treatment options
Abstract
Sepsis remains the leading cause of death in the ICU. Considering the key role of the immune system in sepsis, immunomodulation represents an attractive target for adjunctive therapy. Until recently, clinical trials focused on suppression of the immune system, but this approach failed to improve sepsis outcome. Recent advances in the understanding of sepsis have led to the view that not the initial hyperinflammatory state, but rather a profoundly suppressed state of the immune system, called sepsis-induced immunoparalysis, accounts for the majority of sepsis-related deaths. Immunoparalysis results in ineffective clearance of septic foci, and renders the septic patient more vulnerable to secondary infections, as well as reactivation of latent infections. Several mechanisms behind immunoparalysis have been recognised. Furthermore, due to recognition of the importance of immunoparalysis, immunostimulatory treatment is emerging as a possible adjunctive treatment for sepsis. As such, identification of patients suffering from immunoparalysis using biomarkers is of utmost importance to guide immunostimulatory treatment. In this review, an short overview of the concept of immunoparalysis is presented, while the main focus is on potential biological markers of immunoparalysis and promising immunostimulatory therapeutic agents. The challenging heterogeneity of septic patients in respect to immunomodulatory advances will be discussed, and recommendations for future research are provided.
Similar articles
-
Potentially Inadvertent Immunomodulation: Norepinephrine Use in Sepsis.Am J Respir Crit Care Med. 2016 Sep 1;194(5):550-8. doi: 10.1164/rccm.201604-0862CP. Am J Respir Crit Care Med. 2016. PMID: 27398737
-
New frontiers in precision medicine for sepsis-induced immunoparalysis.Expert Rev Clin Immunol. 2019 Mar;15(3):251-263. doi: 10.1080/1744666X.2019.1562336. Epub 2019 Jan 7. Expert Rev Clin Immunol. 2019. PMID: 30572728 Review.
-
Immunotherapy for the adjunctive treatment of sepsis: from immunosuppression to immunostimulation. Time for a paradigm change?Am J Respir Crit Care Med. 2013 Jun 15;187(12):1287-93. doi: 10.1164/rccm.201301-0036CP. Am J Respir Crit Care Med. 2013. PMID: 23590272 Review.
-
CD4 T Cell Responses and the Sepsis-Induced Immunoparalysis State.Front Immunol. 2020 Jul 7;11:1364. doi: 10.3389/fimmu.2020.01364. eCollection 2020. Front Immunol. 2020. PMID: 32733454 Free PMC article. Review.
-
[Immunomodulation for sepsis: a change of tack?].Ned Tijdschr Geneeskd. 2014;158:A6859. Ned Tijdschr Geneeskd. 2014. PMID: 24518844 Dutch.
Cited by
-
Gut Microbial Membership Modulates CD4 T Cell Reconstitution and Function after Sepsis.J Immunol. 2016 Sep 1;197(5):1692-8. doi: 10.4049/jimmunol.1600940. Epub 2016 Jul 22. J Immunol. 2016. PMID: 27448587 Free PMC article.
-
The protective role of miR-223 in sepsis-induced mortality.Sci Rep. 2020 Oct 19;10(1):17691. doi: 10.1038/s41598-020-74965-2. Sci Rep. 2020. PMID: 33077816 Free PMC article.
-
Phagocytosis-Inflammation Crosstalk in Sepsis: New Avenues for Therapeutic Intervention.Shock. 2020 Nov;54(5):606-614. doi: 10.1097/SHK.0000000000001541. Shock. 2020. PMID: 32516170 Free PMC article. Review.
-
Tracking bacterial DNA patterns in septic progression using 16s rRNA gene amplicon sequencing analysis.Int J Clin Exp Pathol. 2021 Jun 15;14(6):753-767. eCollection 2021. Int J Clin Exp Pathol. 2021. PMID: 34239678 Free PMC article.
-
Dialyzable Leukocyte Extract (Transferon™) Administration in Sepsis: Experience from a Single Referral Pediatric Intensive Care Unit.Biomed Res Int. 2019 Jun 23;2019:8980506. doi: 10.1155/2019/8980506. eCollection 2019. Biomed Res Int. 2019. PMID: 31341910 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials