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Impact of Omicron BA.1 infection on BA.4/5 immunity in transplant recipients.
Ferreira, Victor H; Hu, Queenie; Kurtesi, Alexandra; Solera, Javier T; Ierullo, Matthew; Gingras, Anne-Claude; Kumar, Deepali; Humar, Atul.
  • Ferreira VH; University Health Network, Ajmera Transplant Centre, Toronto, Ontario, Canada.
  • Hu Q; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, Ontario, Canada.
  • Kurtesi A; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, Ontario, Canada.
  • Solera JT; University Health Network, Ajmera Transplant Centre, Toronto, Ontario, Canada.
  • Ierullo M; University Health Network, Ajmera Transplant Centre, Toronto, Ontario, Canada.
  • Gingras AC; Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Sinai Health, Toronto, Ontario, Canada; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
  • Kumar D; University Health Network, Ajmera Transplant Centre, Toronto, Ontario, Canada.
  • Humar A; University Health Network, Ajmera Transplant Centre, Toronto, Ontario, Canada. Electronic address: atul.humar@uhn.ca.
Am J Transplant ; 23(2): 278-283, 2023 02.
Article in English | MEDLINE | ID: covidwho-2259087
ABSTRACT
Mutations in the spike protein of SARS-CoV-2 have allowed Omicron subvariants to escape neutralizing antibodies. The degree to which this occurs in transplant recipients is poorly understood. We measured BA.4/5 cross-neutralizing responses in 75 mostly vaccinated transplant recipients who recovered from BA.1 infection. Sera were collected at 1 and 6 months post-BA.1 infection, and a lentivirus pseudovirus neutralization assay was performed using spike constructs corresponding to BA.1 and BA.4/5. Uninfected immunized transplant recipients and health care worker controls were used for comparison. Following BA.1 infection, the proportion of transplant recipients with neutralizing antibody responses was 88.0% (66/75) against BA.1 and 69.3% (52/75) against BA.4/5 (P = .005). The neutralization level against BA.4/5 was approximately 17-fold lower than that against BA.1 (IQR 10.6- to 45.1-fold lower, P < .0001). BA.4/5 responses declined over time and by ≥0.5 log10 (approximately 3-fold) in almost half of the patients by 6 months. BA.4/5-neutralizing antibody titers in transplant recipients with breakthrough BA.1 infection were similar to those in immunized health care workers but significantly lower than those in uninfected triple-vaccinated transplant recipients. These results provide evidence that transplant recipients are at ongoing risk for BA.4/5 infection despite vaccination and prior Omicron strain infection, and additional mitigation strategies may be required to prevent severe disease in this cohort.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2023 Document Type: Article Affiliation country: J.ajt.2022.10.004

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Humans Language: English Journal: Am J Transplant Journal subject: Transplantation Year: 2023 Document Type: Article Affiliation country: J.ajt.2022.10.004