Exposure to SARS-CoV-2 generates T-cell memory in the absence of a detectable viral infection

T-cell immunity is important for recovery from COVID-19 and provides heightened immunity for re-infection. However, little is known about the SARS-CoV-2-specific T-cell immunity in virus-exposed individuals. Here we report virus-specific CD4 + and CD8 + T-cell memory in recovered COVID-19 patients a...

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Veröffentlicht in:Nature communications 2021-03, Vol.12 (1), p.1724-1724, Article 1724
Hauptverfasser: Wang, Zhongfang, Yang, Xiaoyun, Zhong, Jiaying, Zhou, Yumin, Tang, Zhiqiang, Zhou, Haibo, He, Jun, Mei, Xinyue, Tang, Yonghong, Lin, Bijia, Chen, Zhenjun, McCluskey, James, Yang, Ji, Corbett, Alexandra J., Ran, Pixin
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Sprache:eng
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Zusammenfassung:T-cell immunity is important for recovery from COVID-19 and provides heightened immunity for re-infection. However, little is known about the SARS-CoV-2-specific T-cell immunity in virus-exposed individuals. Here we report virus-specific CD4 + and CD8 + T-cell memory in recovered COVID-19 patients and close contacts. We also demonstrate the size and quality of the memory T-cell pool of COVID-19 patients are larger and better than those of close contacts. However, the proliferation capacity, size and quality of T-cell responses in close contacts are readily distinguishable from healthy donors, suggesting close contacts are able to gain T-cell immunity against SARS-CoV-2 despite lacking a detectable infection. Additionally, asymptomatic and symptomatic COVID-19 patients contain similar levels of SARS-CoV-2-specific T-cell memory. Overall, this study demonstrates the versatility and potential of memory T cells from COVID-19 patients and close contacts, which may be important for host protection. T cells compose a critical component of the immune response to coronavirus infection with SARS-CoV-2. Here the authors characterise the T cell response to SARS CoV-2 in patients and their close contacts, and show the presence of SARS-CoV-2 specific T cells in the absence of detectable virus infection.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-021-22036-z