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SARS-CoV-2 T-cell epitopes define heterologous and COVID-19-induced T-cell recognition

Authors :
Andreas Peter
Michael Fehr
Ulrich Rothbauer
Malte Roerden
Annika Nelde
Tamam Bakchoul
Sebastian Hörber
Jonas Rieth
Philipp D. Kaiser
Nicole Schneiderhan-Marra
Ilona Hagelstein
Gérard Krause
Maren Lübke
Monika Strengert
Markus F. Templin
Marcel Wacker
Vlatka Stos-Zweifel
Jonas S. Heitmann
Daniel J. Kowalewski
Juliane S. Walz
David Rachfalski
Matthias Becker
Beate Preuß
Stefan Stevanovic
Tatjana Bilich
Thomas O. Joos
Cécile Gouttefangeas
Melanie Märklin
Yacine Maringer
Daniel Junker
Michael Graf
Lena-Christin Gruber
Jens Bauer
Bjoern Traenkle
Helmut R. Salih
Reinhild Klein
Oliver Kohlbacher
Hans-Georg Rammensee
Publication Year :
2020
Publisher :
Research Square Platform LLC, 2020.

Abstract

The SARS-CoV-2 pandemic calls for the rapid development of diagnostic, preventive, and therapeutic approaches. CD4+ and CD8+ T cell-mediated immunity is central for control of and protection from viral infections[1-3]. A prerequisite to characterize T-cell immunity, but also for the development of vaccines and immunotherapies, is the identification of the exact viral T-cell epitopes presented on human leukocyte antigens (HLA)[2-8]. This is the first work identifying and characterizing SARS-CoV-2-specific and cross-reactive HLA class I and HLA-DR T-cell epitopes in SARS-CoV-2 convalescents (n = 180) as well as unexposed individuals (n = 185) and confirming their relevance for immunity and COVID-19 disease course. SARS-CoV-2-specific T-cell epitopes enabled detection of post-infectious T-cell immunity, even in seronegative convalescents. Cross-reactive SARS-CoV-2 T-cell epitopes revealed preexisting T-cell responses in 81% of unexposed individuals, and validation of similarity to common cold human coronaviruses provided a functional basis for postulated heterologous immunity[9] in SARS-CoV-2 infection[10,11]. Intensity of T-cell responses and recognition rate of T-cell epitopes was significantly higher in the convalescent donors compared to unexposed individuals, suggesting that not only expansion, but also diversity spread of SARS-CoV-2 T-cell responses occur upon active infection. Whereas anti-SARS-CoV-2 antibody levels were associated with severity of symptoms in our SARS-CoV-2 donors, intensity of T-cell responses did not negatively affect COVID-19 severity. Rather, diversity of SARS-CoV-2 T-cell responses was increased in case of mild symptoms of COVID-19, providing evidence that development of immunity requires recognition of multiple SARS-CoV-2 epitopes. Together, the specific and cross-reactive SARS-CoV-2 T-cell epitopes identified in this work enable the identification of heterologous and post-infectious T-cell immunity and facilitate the development of diagnostic, preventive, and therapeutic measures for COVID-19.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........017668fce0754e232084e99fbeff1065