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A role for human leucocyte antigens in the susceptibility to SARS-Cov-2 infection observed in transplant patients.
Poulton, Kay; Wright, Paul; Hughes, Pamela; Savic, Sinisa; Welberry Smith, Matthew; Guiver, Malcolm; Morton, Muir; van Dellen, David; Tholouli, Eleni; Wynn, Robert; Clark, Brendan.
  • Poulton K; Transplantation Laboratory, Manchester Royal Infirmary, Manchester, UK.
  • Wright P; Manchester Academic Health Science Centre, University of Manchester, Manchester, UK.
  • Hughes P; Transplantation Laboratory, Manchester Royal Infirmary, Manchester, UK.
  • Savic S; Transplant Immunology, St James's University Hospital, Leeds, UK.
  • Welberry Smith M; Department Immunology, St James's University Hospital, Leeds, UK.
  • Guiver M; Department Renal Medicine, St James's University Hospital, Leeds, UK.
  • Morton M; Department Virology, Manchester Royal Infirmary, Manchester, UK.
  • van Dellen D; Department Renal Medicine, Manchester Royal Infirmary, Manchester, UK.
  • Tholouli E; Department Renal Transplantation, Manchester Royal Infirmary, Manchester, UK.
  • Wynn R; Department Haematology, Manchester Royal Infirmary, Manchester, UK.
  • Clark B; Paediatric BMT Unit, Royal Manchester Children's Hospital, Manchester, UK.
Int J Immunogenet ; 47(4): 324-328, 2020 Aug.
Article in English | MEDLINE | ID: covidwho-632057
ABSTRACT
We analysed data from 80 patients who tested positive for SARS-CoV-2 RNA who had previously been HLA typed to support transplantation. Data were combined from two adjacent centres in Manchester and Leeds to achieve a sufficient number for early analysis. HLA frequencies observed were compared against two control populations first, against published frequencies in a UK deceased donor population (n = 10,000) representing the target population of the virus, and second, using a cohort of individuals from the combined transplant waiting lists of both centres (n = 308), representing a comparator group of unaffected individuals of the same demographic. We report a significant HLA association with HLA- DQB1*06 (53% vs. 36%; p < .012; OR 1.96; 95% CI 1.94-3.22) and infection. A bias towards an increased representation of HLA-A*26, HLA-DRB1*15, HLA-DRB1*10 and DRB1*11 was also noted but these were either only significant using the UK donor controls, or did not remain significant after correction for multiple tests. Likewise, HLA-A*02, HLA-B*44 and HLA-C*05 may exert a protective effect, but these associations did not remain significant after correction for multiple tests. This is relevant information for the clinical management of patients in the setting of the current SARS-CoV-2 pandemic and potentially in risk-assessing staff interactions with infected patients.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Histocompatibility Testing / Coronavirus Infections / Genetic Predisposition to Disease / Betacoronavirus Type of study: Cohort study / Observational study / Prognostic study Limits: Humans Language: English Journal: Int J Immunogenet Journal subject: Allergy and Immunology / Genetics Year: 2020 Document Type: Article Affiliation country: Iji.12505

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Histocompatibility Testing / Coronavirus Infections / Genetic Predisposition to Disease / Betacoronavirus Type of study: Cohort study / Observational study / Prognostic study Limits: Humans Language: English Journal: Int J Immunogenet Journal subject: Allergy and Immunology / Genetics Year: 2020 Document Type: Article Affiliation country: Iji.12505