4.6 Article

Positive flow cytometry crossmatch with discrepant antibody testing results following COVID-19 vaccination

期刊

AMERICAN JOURNAL OF TRANSPLANTATION
卷 21, 期 11, 页码 3785-3789

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WILEY
DOI: 10.1111/ajt.16753

关键词

alloantibody; clinical research; practice; crossmatch; histocompatibility; immunobiology; kidney transplantation; nephrology; kidney transplantation; living donor; panel-reactive antibody (PRA); translational research; science; vaccine

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This case study reports a patient awaiting a second kidney transplantation who tested positive for B cell flow cytometry crossmatch 37 days after receiving the COVID-19 vaccine. The emergence of antibodies to HLA-DR7 following vaccination highlights the potential impact of COVID-19 immunization on alloimmunity among transplant candidates. Utilizing multiple assays and history of allo-sensitization is crucial in assessing immunological risks associated with organ transplantation.
The impact of COVID-19 vaccination on the alloimmunity of transplant candidates is unknown. We report a case of positive B cell flow cytometry crossmatch in a patient waiting for second kidney transplantation, 37 days after receiving the COVID-19 vaccine. The preliminary crossmatch, using sample collected before COVID-19 vaccination, was negative. The antibodies to mismatched donor HLA-DR7 were detected only with multi-antigen beads but not with single-antigen beads, excluding possible prozone effects in solid-phase antibody assays. The crossmatches were positive with HLA-DR7-positive surrogates (n = 2) while negative with HLA-DR7-negative surrogates (n = 3), which confirms the HLA-DR7 alloreactivity. The antigen configurations on B lymphocytes are similar to that on the multi-antigen beads while distinct from the single-antigen beads. HLA-DR7 was the repeating mismatched antigen with the failing first kidney allograft. The newly emerged antibody to HLA-DR7 probably is the consequence of bystander activation of memory response by the COVID-19 vaccination. This case highlights the importance of verifying allo-sensitization history and utilizing multiple assays, including cell-based crossmatch and solid-phase assays with multi-antigens. COVID-19 immunization may deserve special attention when assessing the immunological risk before and after organ transplantation.

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