Antibody and T Cell Response to SARS-CoV-2 Messenger RNA BNT162b2 Vaccine in Kidney Transplant Recipients and Hemodialysis Patients
Dominique Bertrand, M. Hamzaoui, Véronique Lemee, Julie Lamulle, M. Hanoy, Charlotte Laurent, L Lebourg, Isabelle Étienne, Mathilde Lemoine, Frank Le Roy, Dorian Nezam, Jean‐Christophe Plantier, Olivier Boyer, Dominique Guerrot, Sophie Candon
Abstract
Significance Statement Antibody and T cell responses to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA vaccines are poorly reported in kidney transplant recipients (KTRs) and patients on hemodialysis (HDPs). The authors investigated the response to BNT162b2 vaccine in 45 KTRs and ten HDPs. After the second dose, 88.9% of HDPs and only 17.8% of KTRs developed anti–SARS-CoV-2 antibodies. A specific T cell response was induced in 100% of HDPs and 57.8% of KTRs. The immune response seemed influenced by the immunosuppressive regimen in KTRs, particularly tacrolimus and belatacept. These results could help to better define the strategy of vaccination in this immunocompromised population. Background Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is associated with a high rate of mortality in patients with ESKD, and vaccination is hoped to prevent infection. Methods Between January 18 and February 24, 2021, 225 kidney transplant recipients (KTRs) and 45 patients on hemodialysis (HDPs) received two injections of mRNA BNT162b2 vaccine. The postvaccinal humoral and cellular response was explored in the first 45 KTRs and ten HDPs. Results After the second dose, eight HDPs (88.9%) and eight KTRs (17.8%) developed antispike SARS-CoV-2 antibodies ( P <0.001). Median titers of antibodies in responders were 1052 AU/ml (IQR, 515–2689) in HDPs and 671 AU/ml (IQR, 172–1523) in KTRs ( P =0.40). Nine HDPs (100%) and 26 KTRs (57.8%) showed a specific T cell response ( P =0.06) after the second injection. In responders, median numbers of spike-reactive T cells were 305 SFCs per 10 6 CD3+ T cells (IQR, 95–947) in HDPs and 212 SFCs per 10 6 CD3+ T cells (IQR, 61–330) in KTRs ( P =0.40). In KTRs, the immune response to BNT162b2 seemed influenced by the immunosuppressive regimen, particularly tacrolimus or belatacept. Conclusion Immunization with BNT162b2 seems more efficient in HDPs, indicating that vaccination should be highly recommended in these patients awaiting a transplant. However, the current vaccinal strategy for KTRs may not provide effective protection against COVID-19 and will likely need to be improved.