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The potential clinical utility of measuring severe acute respiratory syndrome coronavirus 2-specific T-cell responses.
Goletti, Delia; Petrone, Linda; Manissero, Davide; Bertoletti, Antonio; Rao, Sonia; Ndunda, Nduku; Sette, Alessandro; Nikolayevskyy, Vladyslav.
  • Goletti D; Translational Research Unit, National Institute for Infectious Diseases (INMI), "Lazzaro Spallanzani"-IRCCS, Rome, Italy. Electronic address: delia.goletti@inmi.it.
  • Petrone L; Translational Research Unit, National Institute for Infectious Diseases (INMI), "Lazzaro Spallanzani"-IRCCS, Rome, Italy.
  • Manissero D; QIAGEN Manchester Ltd, Manchester, UK.
  • Bertoletti A; Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore; Singapore Immunology Network, A∗STAR, Singapore.
  • Rao S; QIAGEN Inc., Germantown, MD, USA.
  • Ndunda N; Former QIAGEN Employee, 2005 Mada Residences, Downtown Dubai, PO Box 50502, United Arab Emirates.
  • Sette A; Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology (LJI), La Jolla, CA, USA; Department of Medicine, Division of Infectious Diseases and Global Public Health, University of California, San Diego (UCSD), La Jolla, CA, USA.
  • Nikolayevskyy V; QIAGEN Manchester Ltd, Manchester, UK; Department of Infectious Diseases and Immunity, Imperial College, London, UK.
Clin Microbiol Infect ; 27(12): 1784-1789, 2021 Dec.
Article in English | MEDLINE | ID: covidwho-1353821
ABSTRACT

BACKGROUND:

Both humoral and cell-mediated responses are associated with immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although our understanding of the potential role of T-cell responses in the context of coronavirus disease 2019 (COVID-19) is rapidly increasing, more information is still needed.

OBJECTIVES:

To provide an overview of the role of T-cell immunity in COVID-19, in the context of natural infection and post-vaccination, and discuss the potential utility of measuring SARS-CoV-2-specific T-cell responses, drawing on experience of the use of interferon-γ release assays (IGRAs) in tuberculosis (TB). SOURCES PubMed articles up to 16 April 2021. CONTENT T-cell responses can be detected very early in the course of COVID-19, earlier than the detection of antibody responses, and are correlated with COVID-19 outcome. Lower CD4+ and CD8+ T-cell counts are markers of more severe disease, longer duration of viral RNA positivity and increased mortality. In line with natural infection, SARS-CoV-2 vaccination stimulates robust T-cell responses, which probably play an important role in protection; data on long-term T-cell responses are currently limited. The utility of measuring T-cell responses is already well established in both aiding the diagnosis of TB infection using IGRAs, and evaluation of T-cell responses to TB vaccine candidates. A variety of assays have already been developed to measure SARS-CoV-2-specific T-cell responses, including IGRAs, intracellular cytokine staining and activation-induced markers. IGRAs based on SARS-CoV-2 antigens can distinguish between convalescent and uninfected healthy blood donors. IMPLICATIONS Simple assays for measuring the quantity and function of T-cell responses may have utility in the prognostication of COVID-19, and for monitoring immune responses to SARS-CoV-2 vaccination and population-based immunity to SARS-CoV-2 variants of interest.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / COVID-19 / Immunity, Cellular Type of study: Experimental Studies / Prognostic study / Reviews Topics: Vaccines / Variants Limits: Humans Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2021 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / COVID-19 / Immunity, Cellular Type of study: Experimental Studies / Prognostic study / Reviews Topics: Vaccines / Variants Limits: Humans Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2021 Document Type: Article