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Characterization of the SARS-CoV-2-Specific T Cell Responses in Rheumatoid Arthritis Subjects Vaccinated for COVID-19
Jaeyoon Song1, Ricardo da Silva Antunes2, Mehrnaz Agili Seyede3
1School of Medicine, Department of Pediatrics, University of California San Diego, La Jolla, California, USA.
Rheumatoid arthritis patients mount T cell responses to COVID-19 mRNA vaccines, irrespective of injection number. Double-negative T cells may differentiate into CD8+ T cells, potentially worsening RA inflammation.
Area of Science:
- Immunology
- Vaccinology
- Rheumatology
Background:
- Efficacy of mRNA vaccines in autoimmune patients on immunosuppressants is debated.
- Rheumatoid arthritis (RA) patients present diverse disease severities and comorbidities.
- Understanding T cell responses to SARS-CoV-2 vaccination in RA is crucial.
Purpose of the Study:
- To characterize T cell responses to SARS-CoV-2 vaccination in rheumatoid arthritis (RA) patients.
- To investigate the correlation between T cell memory and vaccine boost numbers.
- To explore the role of double-negative (DN) T cells in RA vaccine recipients.
Main Methods:
- Analysis of SARS-CoV-2 specific T cell responses (CD4+, CD8+, Treg) in RA patients post-vaccination.
- Enumeration of non-specific T cells in patients with COVID-19.
- In vitro co-culture of DN T cells with myeloid dendritic cells (DCs).
Main Results:
- RA patients demonstrated circulating spike-specific CD4+ T helper and CD8+ cytotoxic T cells post-vaccination.
- T cell memory did not correlate with the number of vaccine injections received.
- Double-negative (DN) T cells expanded upon SARS-CoV-2 peptide stimulation and differentiated into CD8+ T cells in the presence of DCs.
Conclusions:
- Rheumatoid arthritis patients respond to mRNA COVID-19 vaccines, with T cell response independent of injection count.
- The differentiation of DN T cells into CD8+ T cells may contribute to inflammation in RA vaccine recipients.
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