Severe Acute Respiratory Syndrome Coronavirus 2 Infection Induces Greater T-Cell Responses Compared to Vaccination in Solid Organ Transplant Recipients

被引:12
作者
Ferreira, Victor H. [1 ]
Marinelli, Tina [1 ,2 ]
Ierullo, Matthew [1 ]
Ku, Terrance [1 ]
Hall, Victoria G. [1 ]
Majchrzak-Kita, Beata [1 ]
Kulasingam, Vathany [3 ]
Humar, Atul [1 ]
Kumar, Deepali [1 ]
机构
[1] Univ Hlth Network, Ajmera Transplant Ctr, Toronto, ON, Canada
[2] Royal Prince Alfred Hosp, Dept Infect Dis, Sydney, NSW, Australia
[3] Univ Hlth Network, Lab Med Program, Toronto, ON, Canada
关键词
transplantation; COVID-19; SARS-CoV-2; T cells; vaccination; COVID-19;
D O I
10.1093/infdis/jiab542
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell immunity associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or vaccination in solid organ transplant recipients (SOTRs) is poorly understood. To address this, we measured T-cell responses in 50 SOTRs with prior SARS-CoV-2 infection. The majority of patients mounted SARS-CoV-2-specific CD4+ T-cell responses against spike (S), nucleocapsid, and membrane proteins; CD8+ T-cell responses were generated to a lesser extent. CD4+ T-cell responses correlated with antibody levels. Severity of disease and mycophenolate dose were moderately associated with lower proportions of antigen-specific T cells. Relative to nontransplant controls, SOTRs had perturbations in both total and antigen-specific T cells, including higher frequencies of total PD-1+ CD4+ T cells. Vaccinated SOTRs (n = 55) mounted significantly lower proportions of S-specific polyfunctional CD4+ T cells after 2 doses, relative to unvaccinated SOTRs with prior coronavirus disease 2019. Together, these results suggest that SOTRs generate robust T-cell responses following natural infection that correlate with disease severity but generate comparatively lower T-cell responses following mRNA vaccination.
引用
收藏
页码:1849 / 1860
页数:12
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