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Immunogenicity and Reactogenicity After SARS-CoV-2 mRNA Vaccination in Kidney Transplant Recipients Taking Belatacept.
Ou, Michael T; Boyarsky, Brian J; Chiang, Teresa P Y; Bae, Sunjae; Werbel, William A; Avery, Robin K; Tobian, Aaron A R; Massie, Allan B; Segev, Dorry L; Garonzik-Wang, Jacqueline M.
  • Ou MT; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Boyarsky BJ; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Chiang TPY; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Bae S; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Werbel WA; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Avery RK; Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Tobian AAR; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Massie AB; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Segev DL; Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Garonzik-Wang JM; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Transplantation ; 105(9): 2119-2123, 2021 09 01.
Article in English | MEDLINE | ID: covidwho-1240980
ABSTRACT

BACKGROUND:

Belatacept may impair humoral immunity, impacting the effectiveness of SARS-CoV-2 mRNA vaccines in transplant recipients. We investigated immunogenicity after SARS-CoV-2 mRNA vaccines in kidney transplant recipients who are and are not taking belatacept.

METHODS:

Participants were recruited between December 9, 2020, and April 1, 2021. Blood samples were collected after dose 1 and dose 2 (D1, D2) and analyzed using either an anti-SARS-CoV-2 enzyme immunoassay against the S1 domain of the SARS-CoV-2 spike protein or immunoassay against the receptor-binding domain of the SARS-CoV-2 spike protein. Stabilized inverse probability of treatment weights was used to compare immunogenicity, and a weighted logistics regression was used to calculate fold change of positive response.

RESULTS:

Among the 609 participants studied, 24 (4%) were taking belatacept. After dose 1, 0/24 (0%) belatacept patients had detectable antibodies, compared with 77 of 568 (14%) among the equivalent nonbelatacept population (P = 0.06). After dose 2, 1/19 (5%) belatacept patients had detectable antibodies, compared with 190/381 (50%) among the equivalent nonbelatacept population (P < 0.001). Belatacept use was associated with 16.7-fold lower odds of having a positive post-D2 titer result (P < 0.01).

CONCLUSIONS:

Additional measures need to be explored to protect kidney transplant recipients taking belatacept. Best safety practices should be continued despite vaccination among this population.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Kidney Transplantation / Renal Insufficiency / Immunity, Humoral / Abatacept / COVID-19 / Graft Rejection Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Transplantation Year: 2021 Document Type: Article Affiliation country: TP.0000000000003824

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Full text: Available Collection: International databases Database: MEDLINE Main subject: RNA, Viral / Kidney Transplantation / Renal Insufficiency / Immunity, Humoral / Abatacept / COVID-19 / Graft Rejection Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Transplantation Year: 2021 Document Type: Article Affiliation country: TP.0000000000003824