Sharing CD4+ T Cell Loss: When COVID-19 and HIV Collide on Immune System

Front Immunol. 2020 Dec 15:11:596631. doi: 10.3389/fimmu.2020.596631. eCollection 2020.

Abstract

COVID-19 is a distinctive infection characterized by elevated inter-human transmission and presenting from absence of symptoms to severe cytokine storm that can lead to dismal prognosis. Like for HIV, lymphopenia and drastic reduction of CD4+ T cell counts in COVID-19 patients have been linked with poor clinical outcome. As CD4+ T cells play a critical role in orchestrating responses against viral infections, important lessons can be drawn by comparing T cell response in COVID-19 and in HIV infection and by studying HIV-infected patients who became infected by SARS-CoV-2. We critically reviewed host characteristics and hyper-inflammatory response in these two viral infections to have a better insight on the large difference in clinical outcome in persons being infected by SARS-CoV-2. The better understanding of mechanism of T cell dysfunction will contribute to the development of targeted therapy against severe COVID-19 and will help to rationally design vaccine involving T cell response for the long-term control of viral infection.

Keywords: CD4 exhaustion; COVID-19; HIV; cytokine storm; leaky gut.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology
  • COVID-19 / immunology*
  • COVID-19 / pathology
  • Cytokine Release Syndrome / immunology
  • Cytokine Release Syndrome / pathology
  • Cytokines / blood
  • Dysbiosis / pathology
  • Gastrointestinal Microbiome / physiology
  • HIV Infections / immunology*
  • HIV Infections / pathology
  • Humans
  • Lymphopenia / pathology*
  • SARS-CoV-2 / immunology*
  • Tight Junctions / pathology

Substances

  • Cytokines