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Humoral and cellular immune response and safety of two-dose SARS-CoV-2 mRNA-1273 vaccine in solid organ transplant recipients.
Hall, Victoria G; Ferreira, Victor H; Ierullo, Matthew; Ku, Terrance; Marinelli, Tina; Majchrzak-Kita, Beata; Yousuf, Anila; Kulasingam, Vathany; Humar, Atul; Kumar, Deepali.
  • Hall VG; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Ferreira VH; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Ierullo M; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Ku T; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Marinelli T; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Majchrzak-Kita B; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Yousuf A; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Kulasingam V; Laboratory Medicine Program, University Health Network, Toronto, Canada.
  • Humar A; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
  • Kumar D; Transplant Infectious Diseases and Ajmera Transplant Centre, University Health Network, Toronto, Canada.
Am J Transplant ; 21(12): 3980-3989, 2021 12.
Article in English | MEDLINE | ID: covidwho-1341238
ABSTRACT
Solid organ transplant recipients are at high risk of severe disease from COVID-19. We assessed the immunogenicity of mRNA-1273 vaccine using a combination of antibody testing, surrogate neutralization assays, and T cell assays. Patients were immunized with two doses of vaccine and immunogenicity assessed after each dose using the above tests. CD4+ and CD8+ T cell responses were assessed in a subset using flow-cytometry. A total of 127 patients were enrolled of which 110 provided serum at all time points. A positive anti-RBD antibody was seen in 5.0% after one dose and 34.5% after two doses. Neutralizing antibody was present in 26.9%. Of note, 28.5% of patients with anti-RBD did not have neutralizing antibody. T cell responses in a sub-cohort of 48 patients showed a positive CD4+ T cell response in 47.9%. Of note, in this sub-cohort, 46.2% of patients with a negative anti-RBD, still had a positive CD4+ T cell response. The vaccine was safe and well-tolerated. In summary, immunogenicity of mRNA-1273 COVID-19 vaccine was modest, but a subset of patients still develop neutralizing antibody and CD4+T- cell responses. Importantly polyfunctional CD4+T cell responses were observed in a significant portion who were antibody negative, further highlighting the importance of vaccination in this patient population. IRB Statement This study was approved by the University Health Network Research Ethics Board (CAPCR ID 20-6069).
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organ Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2021 Document Type: Article Affiliation country: Ajt.16766

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Organ Transplantation / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2021 Document Type: Article Affiliation country: Ajt.16766