COVID-19 in people living with HIV: Clinical implications of dynamics of the immune response to SARS-CoV-2

J Med Virol. 2021 Mar;93(3):1796-1804. doi: 10.1002/jmv.26556. Epub 2020 Oct 8.

Abstract

Little evidence on coronavirus disease 2019 (COVID-19) in people living with HIV (PLWH) is currently available. We reported clinical and viroimmunological data of all HIV-positive patients admitted to our center with COVID-19 from March 1 to May 12, 2020. Overall, five patients were included: all were virologically-suppressed on antiretroviral therapy and CD4+ count was greater than 350 cell/mm3 in all but two patients. Although all patients had evidence of pneumonia on admission, only one developed respiratory failure. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA was never detected from nasopharyngeal swabs in two patients, whereas in the others, viral clearance occurred within a maximum of 43 days. Immunoglobulin G production was elicited in all patients and neutralizing antibodies in all but one patient. Specific-T-cell response developed in all patients but was stronger in those with the more severe presentations. Similarly, the highest level of proinflammatory cytokines was found in the only patient experiencing respiratory failure. Despite a mild presentation, patients with more pronounced immunosuppression showed high degrees of both cytokines production and immune activation. Our study did not find an increased risk and severity of COVID-19 in PLWH. Adaptative cellular immune response to SARS-CoV-2 appeared to correlate to disease severity. The mild clinical picture showed in advanced HIV patients, despite a significant T-cell activation and inflammatory profile, suggests a potential role of HIV-driven immunological dysregulation in avoiding immune-pathogenetic processes. However, other possible explanations, as a protective role of certain antiretroviral drugs, should be considered. Further larger studies are needed to better clarify the impact of HIV infection on COVID-19.

Keywords: COVID-19; HIV infection; SARS-CoV-2; immune response.

MeSH terms

  • Anti-Retroviral Agents / therapeutic use*
  • Antibodies, Neutralizing / blood
  • Antibodies, Viral / blood
  • CD4 Lymphocyte Count
  • COVID-19 Drug Treatment*
  • Coinfection / virology
  • Cytokines / blood
  • Female
  • HIV Infections / drug therapy*
  • HIV Integrase Inhibitors / therapeutic use
  • Heterocyclic Compounds, 3-Ring / therapeutic use
  • Humans
  • Immunity, Humoral / immunology
  • Male
  • Middle Aged
  • Oxazines / therapeutic use
  • Piperazines / therapeutic use
  • Pyridones / therapeutic use
  • RNA, Viral / analysis
  • Reverse Transcriptase Inhibitors / therapeutic use
  • Risk
  • SARS-CoV-2 / drug effects*
  • Severity of Illness Index
  • Tenofovir / therapeutic use
  • Transgender Persons

Substances

  • Anti-Retroviral Agents
  • Antibodies, Neutralizing
  • Antibodies, Viral
  • Cytokines
  • HIV Integrase Inhibitors
  • Heterocyclic Compounds, 3-Ring
  • Oxazines
  • Piperazines
  • Pyridones
  • RNA, Viral
  • Reverse Transcriptase Inhibitors
  • Tenofovir
  • dolutegravir