Magnitude and dynamics of the T-cell response to SARS-CoV-2 infection at both individual and population levels.

Introduction

T cells are involved in the early identification and clearance of viral infections and also support the development of antibodies by B cells. This central role for T cells makes them a desirable target for assessing the immune response to SARS-CoV-2 infection.

Methods

Here, we combined two high-throughput immune profiling methods to create a quantitative picture of the T-cell response to SARS-CoV-2. First, at the individual level, we deeply characterized 3 acutely infected and 58 recovered COVID-19 subjects by experimentally mapping their CD8 T-cell response through antigen stimulation to 545 Human Leukocyte Antigen (HLA) class I presented viral peptides. Then, at the population level, we performed T-cell repertoire sequencing on 1,815 samples (from 1,521 COVID-19 subjects) as well as 3,500 controls to identify shared "public" T-cell receptors (TCRs) associated with SARS-CoV-2 infection from both CD8 and CD4 T cells.

Results

Collectively, our data reveal that CD8 T-cell responses are often driven by a few immunodominant, HLA-restricted epitopes. As expected, the T-cell response to SARS-CoV-2 peaks about one to two weeks after infection and is detectable for at least several months after recovery. As an application of these data, we trained a classifier to diagnose SARS-CoV-2 infection based solely on TCR sequencing from blood samples, and observed, at 99.8% specificity, high early sensitivity soon after diagnosis (Day 3-7 = 85.1% [95% CI = 79.9-89.7]; Day 8-14 = 94.8% [90.7-98.4]) as well as lasting sensitivity after recovery (Day 29+/convalescent = 95.4% [92.1-98.3]).

Discussion

The approaches described in this work provide detailed insights into the adaptive immune response to SARS-CoV-2 infection, and they have potential applications in clinical diagnostics, vaccine development, and monitoring.

Copyright © 2025 Snyder, Gittelman, Klinger, May, Osborne, Taniguchi, Jabran Zahid, Kaplan, Dines, Noakes, Pandya, Chen, Elasady, Svejnoha, Ebert, Pesesky, De Almeida, O’Donnell, DeGottardi, Keitany, Lu, Vong, Elyanow, Fields, Al-Asadi, Greissl, Baldo, Semprini, Cerchione, Nicolini, Mazza, Delmonte, Dobbs, Laguna-Goya, Carreño-Tarragona, Barrio, Imberti, Sottini, Quiros-Roldan, Rossi, Biondi, Bettini, D’Angio, Bonfanti, Tompkins, Alba, Dalgard, Sambri, Martinelli, Goldman, Heath, Su, Notarangelo, Paz-Artal, Martinez-Lopez, Howie, Carlson and Robins.

Overview publication

TitleMagnitude and dynamics of the T-cell response to SARS-CoV-2 infection at both individual and population levels.
Date2024-01-01
Issue nameFrontiers in immunology
Issue numberv15:1488860
DOI10.3389/fimmu.2024.1488860
PubMed39840037
AuthorsSnyder TM, Gittelman RM, Klinger M, May DH, Osborne EJ, Taniguchi R, Jabran Zahid H, Kaplan IM, Dines JN, Noakes MT, Pandya R, Chen X, Elasady S, Svejnoha E, Ebert P, Pesesky MW, De Almeida P, O'Donnell H, DeGottardi Q, Keitany G, Lu J, Vong A, Elyanow R, Fields P, Al-Asadi H, Greissl J, Baldo L, Semprini S, Cerchione C, Nicolini F, Mazza M, Delmonte OM, Dobbs K, Laguna-Goya R, Carreño-Tarragona G, Barrio S, Imberti L, Sottini A, Quiros-Roldan E, Rossi C, Biondi A, Bettini LR, D'Angio M, Bonfanti P, Tompkins MF, Alba C, Dalgard C, Sambri V, Martinelli G, Goldman JD, Heath JR, Su HC, Notarangelo LD, Paz-Artal E, Martinez-Lopez J, Howie B, Carlson JM & Robins HS
KeywordsCOVID-19, SARS-CoV-2, T cell, TCR repertoire, cellular immunity, immune response
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