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Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels

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. Here, we combined two high-throughput i...

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Autores principales: Snyder, Thomas M., Gittelman, Rachel M., Klinger, Mark, May, Damon H., Osborne, Edward J., Taniguchi, Ruth, Zahid, H. Jabran, Kaplan, Ian M., Dines, Jennifer N., Noakes, Matthew T., Pandya, Ravi, Chen, Xiaoyu, Elasady, Summer, Svejnoha, Emily, Ebert, Peter, Pesesky, Mitchell W., De Almeida, Patricia, O’Donnell, Hope, DeGottardi, Quinn, Keitany, Gladys, Lu, Jennifer, Vong, Allen, Elyanow, Rebecca, Fields, Paul, Greissl, Julia, Baldo, Lance, Semprini, Simona, Cerchione, Claudio, Nicolini, Fabio, Mazza, Massimiliano, Delmonte, Ottavia M., Dobbs, Kerry, Laguna-Goya, Rocio, Carreño-Tarragona, Gonzalo, Barrio, Santiago, Imberti, Luisa, Sottini, Alessandra, Quiros-Roldan, Eugenia, Rossi, Camillo, Biondi, Andrea, Bettini, Laura Rachele, D’Angio, Mariella, Bonfanti, Paolo, Tompkins, Miranda F., Alba, Camille, Dalgard, Clifton, Sambri, Vittorio, Martinelli, Giovanni, Goldman, Jason D., Heath, James R., Su, Helen C., Notarangelo, Luigi D., Paz-Artal, Estela, Martinez-Lopez, Joaquin, Carlson, Jonathan M., Robins, Harlan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418734/
https://www.ncbi.nlm.nih.gov/pubmed/32793919
http://dx.doi.org/10.1101/2020.07.31.20165647
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author Snyder, Thomas M.
Gittelman, Rachel M.
Klinger, Mark
May, Damon H.
Osborne, Edward J.
Taniguchi, Ruth
Zahid, H. Jabran
Kaplan, Ian M.
Dines, Jennifer N.
Noakes, Matthew T.
Pandya, Ravi
Chen, Xiaoyu
Elasady, Summer
Svejnoha, Emily
Ebert, Peter
Pesesky, Mitchell W.
De Almeida, Patricia
O’Donnell, Hope
DeGottardi, Quinn
Keitany, Gladys
Lu, Jennifer
Vong, Allen
Elyanow, Rebecca
Fields, Paul
Greissl, Julia
Baldo, Lance
Semprini, Simona
Cerchione, Claudio
Nicolini, Fabio
Mazza, Massimiliano
Delmonte, Ottavia M.
Dobbs, Kerry
Laguna-Goya, Rocio
Carreño-Tarragona, Gonzalo
Barrio, Santiago
Imberti, Luisa
Sottini, Alessandra
Quiros-Roldan, Eugenia
Rossi, Camillo
Biondi, Andrea
Bettini, Laura Rachele
D’Angio, Mariella
Bonfanti, Paolo
Tompkins, Miranda F.
Alba, Camille
Dalgard, Clifton
Sambri, Vittorio
Martinelli, Giovanni
Goldman, Jason D.
Heath, James R.
Su, Helen C.
Notarangelo, Luigi D.
Paz-Artal, Estela
Martinez-Lopez, Joaquin
Carlson, Jonathan M.
Robins, Harlan S.
author_facet Snyder, Thomas M.
Gittelman, Rachel M.
Klinger, Mark
May, Damon H.
Osborne, Edward J.
Taniguchi, Ruth
Zahid, H. Jabran
Kaplan, Ian M.
Dines, Jennifer N.
Noakes, Matthew T.
Pandya, Ravi
Chen, Xiaoyu
Elasady, Summer
Svejnoha, Emily
Ebert, Peter
Pesesky, Mitchell W.
De Almeida, Patricia
O’Donnell, Hope
DeGottardi, Quinn
Keitany, Gladys
Lu, Jennifer
Vong, Allen
Elyanow, Rebecca
Fields, Paul
Greissl, Julia
Baldo, Lance
Semprini, Simona
Cerchione, Claudio
Nicolini, Fabio
Mazza, Massimiliano
Delmonte, Ottavia M.
Dobbs, Kerry
Laguna-Goya, Rocio
Carreño-Tarragona, Gonzalo
Barrio, Santiago
Imberti, Luisa
Sottini, Alessandra
Quiros-Roldan, Eugenia
Rossi, Camillo
Biondi, Andrea
Bettini, Laura Rachele
D’Angio, Mariella
Bonfanti, Paolo
Tompkins, Miranda F.
Alba, Camille
Dalgard, Clifton
Sambri, Vittorio
Martinelli, Giovanni
Goldman, Jason D.
Heath, James R.
Su, Helen C.
Notarangelo, Luigi D.
Paz-Artal, Estela
Martinez-Lopez, Joaquin
Carlson, Jonathan M.
Robins, Harlan S.
author_sort Snyder, Thomas M.
collection PubMed
description 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. 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 (class II data in a forthcoming study). 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. 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]). These results demonstrate an approach to reliably assess the adaptive immune response both soon after viral antigenic exposure (before antibodies are typically detectable) as well as at later time points. This blood-based molecular approach to characterizing the cellular immune response has applications in clinical diagnostics as well as in vaccine development and monitoring.
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spelling pubmed-74187342020-08-13 Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels Snyder, Thomas M. Gittelman, Rachel M. Klinger, Mark May, Damon H. Osborne, Edward J. Taniguchi, Ruth Zahid, H. Jabran Kaplan, Ian M. Dines, Jennifer N. Noakes, Matthew T. Pandya, Ravi Chen, Xiaoyu Elasady, Summer Svejnoha, Emily Ebert, Peter Pesesky, Mitchell W. De Almeida, Patricia O’Donnell, Hope DeGottardi, Quinn Keitany, Gladys Lu, Jennifer Vong, Allen Elyanow, Rebecca Fields, Paul Greissl, Julia Baldo, Lance Semprini, Simona Cerchione, Claudio Nicolini, Fabio Mazza, Massimiliano Delmonte, Ottavia M. Dobbs, Kerry Laguna-Goya, Rocio Carreño-Tarragona, Gonzalo Barrio, Santiago Imberti, Luisa Sottini, Alessandra Quiros-Roldan, Eugenia Rossi, Camillo Biondi, Andrea Bettini, Laura Rachele D’Angio, Mariella Bonfanti, Paolo Tompkins, Miranda F. Alba, Camille Dalgard, Clifton Sambri, Vittorio Martinelli, Giovanni Goldman, Jason D. Heath, James R. Su, Helen C. Notarangelo, Luigi D. Paz-Artal, Estela Martinez-Lopez, Joaquin Carlson, Jonathan M. Robins, Harlan S. medRxiv Article 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. 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 (class II data in a forthcoming study). 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. 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]). These results demonstrate an approach to reliably assess the adaptive immune response both soon after viral antigenic exposure (before antibodies are typically detectable) as well as at later time points. This blood-based molecular approach to characterizing the cellular immune response has applications in clinical diagnostics as well as in vaccine development and monitoring. Cold Spring Harbor Laboratory 2020-09-17 /pmc/articles/PMC7418734/ /pubmed/32793919 http://dx.doi.org/10.1101/2020.07.31.20165647 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Article
Snyder, Thomas M.
Gittelman, Rachel M.
Klinger, Mark
May, Damon H.
Osborne, Edward J.
Taniguchi, Ruth
Zahid, H. Jabran
Kaplan, Ian M.
Dines, Jennifer N.
Noakes, Matthew T.
Pandya, Ravi
Chen, Xiaoyu
Elasady, Summer
Svejnoha, Emily
Ebert, Peter
Pesesky, Mitchell W.
De Almeida, Patricia
O’Donnell, Hope
DeGottardi, Quinn
Keitany, Gladys
Lu, Jennifer
Vong, Allen
Elyanow, Rebecca
Fields, Paul
Greissl, Julia
Baldo, Lance
Semprini, Simona
Cerchione, Claudio
Nicolini, Fabio
Mazza, Massimiliano
Delmonte, Ottavia M.
Dobbs, Kerry
Laguna-Goya, Rocio
Carreño-Tarragona, Gonzalo
Barrio, Santiago
Imberti, Luisa
Sottini, Alessandra
Quiros-Roldan, Eugenia
Rossi, Camillo
Biondi, Andrea
Bettini, Laura Rachele
D’Angio, Mariella
Bonfanti, Paolo
Tompkins, Miranda F.
Alba, Camille
Dalgard, Clifton
Sambri, Vittorio
Martinelli, Giovanni
Goldman, Jason D.
Heath, James R.
Su, Helen C.
Notarangelo, Luigi D.
Paz-Artal, Estela
Martinez-Lopez, Joaquin
Carlson, Jonathan M.
Robins, Harlan S.
Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title_full Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title_fullStr Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title_full_unstemmed Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title_short Magnitude and Dynamics of the T-Cell Response to SARS-CoV-2 Infection at Both Individual and Population Levels
title_sort magnitude and dynamics of the t-cell response to sars-cov-2 infection at both individual and population levels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418734/
https://www.ncbi.nlm.nih.gov/pubmed/32793919
http://dx.doi.org/10.1101/2020.07.31.20165647
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