pISSN 3022-6783
eISSN 3022-7712

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Korean J Transplant 2021; 35(Suppl 1): S77-S77

Published online October 7, 2021

https://doi.org/10.4285/ATW2021.OP-1026

© The Korean Society for Transplantation

Acute T cell-mediated rejection after administration of the BNT162b2 mRNA COVID-19 vaccine in a kidney transplant recipient without a history of acute rejection for 13 years: a case report

Hye-won Jang1, Sung Shin2

1Department of Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea
2Department of Surgery-Transplantation, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

Correspondence to: Sung Shin
E-mail:sshin@amc.seoul.kr

Abstract

Background: Kidney transplant recipients have significantly high risks of mortality and morbidity after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, suggesting the need for earlier administration of coronavirus disease 2019 (COVID-19) vaccines in these individuals. However, there is limited data on the humoral and cellular responses after COVID-19 vaccination.
Case report: We report the case of a 78-year-old kidney transplant recipient who experienced acute T cell-mediated rejection (TCMR) after receiving the second dose of the BNT162b2 mRNA COVID-19 vaccine (Pfizer-BioNTech). The recipient underwent deceased donor kidney transplantation for hypertension 13 years ago, and had not experienced any adverse event after transplantation. Her maintenance immunosuppressants were tacrolimus, azathioprine, and low-dose steroid. The latest level of serum creatinine 1 month before the vaccination was 0.61 mg/dL and the trough level of tacrolimus was maintained at 4–5 ng/mL. Fifteen days after receiving the second dose of the BNT162b2 vaccine, the recipient visited our center with a mild headache and fever. The level of serum creatinine was elevated to 4.95 mg/dL, and there was considerable swelling of the transplanted kidney on non-enhanced computerized tomography. On kidney biopsy, acute TCMR (grade IB) was diagnosed with no pathologic evidence of antibody-mediated rejection. Luminex single-antigen flow beads assay did not reveal donor-specific anti-HLA antibodies. Anti-SARS-CoV-2 spike IgG and IgM antibodies (S1-IgG and S1-IgM) were measured by enzyme-linked immunosorbent assay (ELISA) on the day of the kidney biopsy (18 days after the second vaccination), which revealed that the levels of S1-IgG and S1-IgM were 2.80 (weak positive) and 0.16 (negative), respectively. The recipient was administered with steroid pulses (500 mg/day) for 5 days. One month after the steroid pulse therapy, her serum creatinine level had decreased to 2.47 mg/mL.
Conclusions: This report shows that kidney transplant recipients may be at risk for acute rejection after COVID-19 vaccination despite having low levels of S1-IgG and S1-IgM.