T cell and antibody responses to SARS-CoV-2: Experience from a French transplantation and hemodialysis center during the COVID-19 pandemic

被引:36
作者
Candon, Sophie [1 ,2 ]
Guerrot, Dominique [3 ]
Drouot, Laurent [2 ]
Lemoine, Mathilde [3 ]
Lebourg, Ludivine [3 ]
Hanoy, Melanie [3 ]
Boyer, Olivier [1 ,2 ]
Bertrand, Dominique [3 ]
机构
[1] Rouen Univ Hosp, Dept Immunol & Biotherapies, Rouen, France
[2] Univ Rouen Normandy, INSERM U1234, Rouen, France
[3] Rouen Univ Hosp, Dept Nephrol Transplantat & Hemodialysis, Rouen, France
关键词
immunobiology; infection and infectious agents ‐ viral; kidney transplantation; nephrology; monitoring; immune; translational research; science;
D O I
10.1111/ajt.16348
中图分类号
R61 [外科手术学];
学科分类号
摘要
Immunosuppressed organ-transplanted patients are considered at risk for severe forms of COVID-19. Moreover, exaggerated innate and adaptive immune responses might be involved in severe progression of the disease. However, no data on the immune response to SARS-CoV-2 in transplanted patients are currently available. Here, we report the first assessment of antibody and T cell responses to SARS-CoV-2 in 11 kidney-transplanted patients recovered from RT-PCR-confirmed (n = 5) or initially suspected (n = 6) COVID-19. After reduction of immunosuppressive therapy, RT-PCR-confirmed COVID-19 transplant patients were able to mount vigorous antiviral T cell and antibody responses, as efficiently as two nontherapeutically immunosuppressed COVID-19 patients on hemodialysis. By contrast, six RT-PCR-negative patients displayed no antibody response. Among them, three showed very low numbers of SARS-CoV-2-reactive T cells, whereas no T cell response was detected in the other three, potentially ruling out COVID-19 diagnosis. Low levels of T cell reactivity to SARS-CoV-2 were also detected in seronegative healthy controls without known exposure to the virus. These results suggest that during COVID-19, monitoring both T cell and serological immunity might be helpful for the differential diagnosis of COVID-19 but are also needed to evaluate a potential role of antiviral T cells in the development of severe forms of the disease.
引用
收藏
页码:854 / 863
页数:10
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