Asymptomatic SARS-CoV-2 Infection Is Associated With Higher Levels of Serum IL-17C, Matrix Metalloproteinase 10 and Fibroblast Growth Factors Than Mild Symptomatic COVID-19.

COVID-19 SARS-CoV-2 antibodies asymptomatic inflammation innate immunity proteomics serum

Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2022
Historique:
received: 24 11 2021
accepted: 11 03 2022
entrez: 28 4 2022
pubmed: 29 4 2022
medline: 30 4 2022
Statut: epublish

Résumé

Young adults infected with SARS-CoV-2 are frequently asymptomatic or develop only mild disease. Because capturing representative mild and asymptomatic cases require active surveillance, they are less characterized than moderate or severe cases of COVID-19. However, a better understanding of SARS-CoV-2 asymptomatic infections might shed light into the immune mechanisms associated with the control of symptoms and protection. To this aim, we have determined the temporal dynamics of the humoral immune response, as well as the serum inflammatory profile, of mild and asymptomatic SARS-CoV-2 infections in a cohort of 172 initially seronegative prospectively studied United States Marine recruits, 149 of whom were subsequently found to be SARS-CoV-2 infected. The participants had blood samples taken, symptoms surveyed and PCR tests for SARS-CoV-2 performed periodically for up to 105 days. We found similar dynamics in the profiles of viral load and in the generation of specific antibody responses in asymptomatic and mild symptomatic participants. A proteomic analysis using an inflammatory panel including 92 analytes revealed a pattern of three temporal waves of inflammatory and immunoregulatory mediators, and a return to baseline for most of the inflammatory markers by 35 days post-infection. We found that 23 analytes were significantly higher in those participants that reported symptoms at the time of the first positive SARS-CoV-2 PCR compared with asymptomatic participants, including mostly chemokines and cytokines associated with inflammatory response or immune activation (i.e., TNF-α, TNF-β, CXCL10, IL-8). Notably, we detected 7 analytes (IL-17C, MMP-10, FGF-19, FGF-21, FGF-23, CXCL5 and CCL23) that were higher in asymptomatic participants than in participants with symptoms; these are known to be involved in tissue repair and may be related to the control of symptoms. Overall, we found a serum proteomic signature that differentiates asymptomatic and mild symptomatic infections in young adults, including potential targets for developing new therapies and prognostic tests.

Identifiants

pubmed: 35479098
doi: 10.3389/fimmu.2022.821730
pmc: PMC9037090
doi:

Substances chimiques

Interleukin-17 0
Fibroblast Growth Factors 62031-54-3
MMP10 protein, human EC 3.4.24.22
Matrix Metalloproteinase 10 EC 3.4.24.22

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

821730

Informations de copyright

Copyright © 2022 Soares-Schanoski, Sauerwald, Goforth, Periasamy, Weir, Lizewski, Lizewski, Ge, Kuzmina, Nair, Vangeti, Marjanovic, Cappuccio, Cheng, Mofsowitz, Miller, Yu, George, Zaslavsky, Bukreyev, Troyanskaya, Sealfon, Letizia and Ramos.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Alessandra Soares-Schanoski (A)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Natalie Sauerwald (N)

Center for Computational Biology, Flatiron Institute, New York, NY, United States.

Carl W Goforth (CW)

Naval Medical Research Center, Silver Spring, MD, United States.

Sivakumar Periasamy (S)

Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Galveston National Laboratory, Galveston, TX, United States.

Dawn L Weir (DL)

Naval Medical Research Center, Silver Spring, MD, United States.

Stephen Lizewski (S)

Naval Medical Research Unit 6, Lima, Peru.

Rhonda Lizewski (R)

Naval Medical Research Unit 6, Lima, Peru.

Yongchao Ge (Y)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Natalia A Kuzmina (NA)

Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Galveston National Laboratory, Galveston, TX, United States.

Venugopalan D Nair (VD)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Sindhu Vangeti (S)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Nada Marjanovic (N)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Antonio Cappuccio (A)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Wan Sze Cheng (WS)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Sagie Mofsowitz (S)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Clare M Miller (CM)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Xuechen B Yu (XB)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Mary-Catherine George (MC)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Elena Zaslavsky (E)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Alexander Bukreyev (A)

Department of Pathology, University of Texas Medical Branch, Galveston, TX, United States.
Galveston National Laboratory, Galveston, TX, United States.
Department of Microbiology & Immunology, University of Texas Medical Branch, Galveston, TX, United States.

Olga G Troyanskaya (OG)

Center for Computational Biology, Flatiron Institute, New York, NY, United States.
Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, United States.
Department of Computer Science, Princeton University, Princeton, NJ, United States.

Stuart C Sealfon (SC)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Andrew G Letizia (AG)

Naval Medical Research Center, Silver Spring, MD, United States.

Irene Ramos (I)

Department of Neurology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

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