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10.1097/COH.0000000000000655

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suck abstract from ncbi


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pmid33165008      Curr+Opin+HIV+AIDS 2021 ; 16 (1): 36-47
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  • The single-cell landscape of immunological responses of CD4+ T cells in HIV versus severe acute respiratory syndrome coronavirus 2 #MMPMID33165008
  • Collora JA; Liu R; Albrecht K; Ho YC
  • Curr Opin HIV AIDS 2021[Jan]; 16 (1): 36-47 PMID33165008show ga
  • PURPOSE OF REVIEW: CD4 T cell loss is the hallmark of uncontrolled HIV-1 infection. Strikingly, CD4 T cell depletion is a strong indicator for disease severity in the recently emerged coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. We reviewed recent single-cell immune profiling studies in HIV-1 infection and COVID-19 to provide critical insight in virus-induced immunopathogenesis. RECENT FINDINGS: Cytokine dysregulation in HIV-1 leads to chronic inflammation, while severe SARS-CoV-2 infection induces cytokine release syndrome and increased mortality. HIV-1-specific CD4 T cells are dysfunctional, while SARS-CoV-2-specific CD4 T cells exhibit robust Th1 function and correlate with protective antibody responses. In HIV-1 infection, follicular helper T cells (TFH) are susceptible to HIV-1 infection and persist in immune-sanctuary sites in lymphoid tissues as an HIV-1 reservoir. In severe SARS-CoV-2 infection, TFH are absent in lymphoid tissues and are associated with diminished protective immunity. Advancement in HIV-1 DNA, RNA, and protein-based single-cell capture methods can overcome the rarity and heterogeneity of HIV-1-infected cells and identify mechanisms of HIV-1 persistence and clonal expansion dynamics. SUMMARY: Single-cell immune profiling identifies a high-resolution picture of immune dysregulation in HIV-1 and SARS-CoV-2 infection and informs outcome prediction and therapeutic interventions.
  • |Animals[MESH]
  • |CD4-Positive T-Lymphocytes/*immunology[MESH]
  • |COVID-19/genetics/*immunology/virology[MESH]
  • |Cytokines/genetics/immunology[MESH]
  • |HIV Infections/genetics/*immunology/virology[MESH]
  • |Humans[MESH]
  • |Pandemics[MESH]


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