Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Mar 5:5:5-5.
doi: 10.17879/freeneuropathology-2024-5343. eCollection 2024 Jan.

HIV and COVID-19: two pandemics with significant (but different) central nervous system complications

Affiliations

HIV and COVID-19: two pandemics with significant (but different) central nervous system complications

Shino Magaki et al. Free Neuropathol. .

Abstract

Human immunodeficiency virus (HIV) and severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) cause significant neurologic disease. Central nervous system (CNS) involvement of HIV has been extensively studied, with well-documented invasion of HIV into the brain in the initial stage of infection, while the acute effects of SARS-CoV-2 in the brain are unclear. Neuropathologic features of active HIV infection in the brain are well characterized whereas neuropathologic findings in acute COVID-19 are largely non-specific. On the other hand, neuropathologic substrates of chronic dysfunction in both infections, as HIV-associated neurocognitive disorders (HAND) and post-COVID conditions (PCC)/long COVID are unknown. Thus far, neuropathologic studies on patients with HAND in the era of combined antiretroviral therapy have been inconclusive, and autopsy studies on patients diagnosed with PCC have yet to be published. Further longitudinal, multidisciplinary studies on patients with HAND and PCC and neuropathologic studies in comparison to controls are warranted to help elucidate the mechanisms of CNS dysfunction in both conditions.

Keywords: COVID-19; HIV; HIV-associated neurocognitive disorders; Long COVID; Neuropathology; Post-COVID conditions.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Neuropathologic findings in COVID-19 and HIV infection. A) Acute/subacute microinfarct (arrows) in the internal capsule and B) sparse leptomeningeal (arrow) and parenchymal (arrowhead) T lymphocytes highlighted by CD3 immunohistochemistry in patients with COVID-19. C) HIV encephalitis with multinucleated giant cells (arrows) and D) microglial activation (arrowheads) highlighted by immunohistochemistry for Iba-1 in patients with HIV infection. Scale bars: A = 50 μm, B,D = 100 μm, C = 20 μm
Figure 2
Figure 2
Potential mechanisms of neurologic disease in acute/chronic HIV infection and COVID-19/PCC. HAND, HIV-associated neurocognitive disorders; PCC, post-COVID conditions. Figure was created using BioRender.

Similar articles

References

    1. Ruelas DS, Greene WC. An integrated overview of HIV-1 latency. Cell 2013;155:519–29. 10.1016/j.cell.2013.09.044. - DOI - PMC - PubMed
    1. Gottlieb MS, Schroff R, Schanker HM, Weisman JD, Fan PT, Wolf RA, et al. Pneumocystis carinii pneumonia and mucosal candidiasis in previously healthy homosexual men: evidence of a new acquired cellular immunodeficiency. N Engl J Med 1981;305:1425–31. 10.1056/NEJM198112103052401. - DOI - PubMed
    1. Greene WC. A history of AIDS: Looking back to see ahead. Eur J Immunol 2007;37:94–102. 10.1002/eji.200737441. - DOI - PubMed
    1. Barré-Sinoussi F, Chermann JC, Rey F, Nugeyre MT, Chamaret S, Gruest J, et al. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science 1983;220:868–71. 10.1126/science.6189183. - DOI - PubMed
    1. Popovic M, Sarngadharan MG, Read E, Gallo RC. Detection, isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. Science 1984;224:497–500. 10.1126/science.6200935. - DOI - PubMed