Prolonged T-cell activation and long COVID symptoms independently associate with severe COVID-19 at 3 months

Author:

Santopaolo Marianna1ORCID,Gregorova Michaela1ORCID,Hamilton Fergus2,Arnold David2,Long Anna3,Lacey Aurora1,Oliver Elizabeth1ORCID,Halliday Alice1,Baum Holly1ORCID,Hamilton Kristy1,Milligan Rachel1,Pearce Olivia3,Knezevic Lea4,Morales Aza Begonia1,Milne Alice2,Milodowski Emily4,Jones Eben1,Lazarus Rajeka5,Goenka Anu16,Finn Adam167,Maskell Nicholas2,Davidson Andrew D1ORCID,Gillespie Kathleen3,Wooldridge Linda4ORCID,Rivino Laura1ORCID

Affiliation:

1. School of Cellular and Molecular Medicine, University of Bristol

2. Academic Respiratory Unit, North Bristol NHS Trust

3. Diabetes and Metabolism, Bristol Medical School, University of Bristol

4. Bristol Veterinary School, University of Bristol

5. University Hospitals Bristol and Weston NHS Foundation Trust

6. Department of Paediatric Immunology and Infectious Diseases, Bristol Royal Hospital for Children

7. School of Population Health Sciences, University of Bristol

Abstract

Coronavirus disease-19 (COVID-19) causes immune perturbations which may persist long term, and patients frequently report ongoing symptoms for months after recovery. We assessed immune activation at 3–12 months post hospital admission in 187 samples from 63 patients with mild, moderate, or severe disease and investigated whether it associates with long COVID. At 3 months, patients with severe disease displayed persistent activation of CD4+ and CD8+ T-cells, based on expression of HLA-DR, CD38, Ki67, and granzyme B, and elevated plasma levels of interleukin-4 (IL-4), IL-7, IL-17, and tumor necrosis factor-alpha (TNF-α) compared to mild and/or moderate patients. Plasma from severe patients at 3 months caused T-cells from healthy donors to upregulate IL-15Rα, suggesting that plasma factors in severe patients may increase T-cell responsiveness to IL-15-driven bystander activation. Patients with severe disease reported a higher number of long COVID symptoms which did not however correlate with cellular immune activation/pro-inflammatory cytokines after adjusting for age, sex, and disease severity. Our data suggests that long COVID and persistent immune activation may correlate independently with severe disease.

Funder

Wellcome Trust

Southmead Hospital Charity

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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