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GWAS Study

Human genomics of the humoral immune response against polyomaviruses.

Hodel F, Chong AY, Scepanovic P et al.

34532061 PubMed ID
GWAS Study Type
15403 Participants
34 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HF
Hodel F
CA
Chong AY
SP
Scepanovic P
XZ
Xu ZM
NO
Naret O
TC
Thorball CW
RS
Rüeger S
MP
Marques-Vidal P
VP
Vollenweider P
BM
Begemann M
EH
Ehrenreich H
BN
Brenner N
BN
Bender N
WT
Waterboer T
MA
Mentzer AJ
HA
Hill AVS
HC
Hammer C
FJ
Fellay J
Chapter II

Abstract

Summary of the research findings

Human polyomaviruses are widespread in humans and can cause severe disease in immunocompromised individuals. To identify human genetic determinants of the humoral immune response against polyomaviruses, we performed genome-wide association studies and meta-analyses of qualitative and quantitative immunoglobulin G responses against BK polyomavirus (BKPyV), JC polyomavirus (JCPyV), Merkel cellpolyomavirus (MCPyV), WU polyomavirus (WUPyV), and human polyomavirus 6 (HPyV6) in 15,660 individuals of European ancestry from three independent studies. We observed significant associations for all tested viruses: JCPyV, HPyV6, and MCPyV associated with human leukocyte antigen class II variation, BKPyV and JCPyV with variants in FUT2, responsible for secretor status, MCPyV with variants in STING1, involved in interferon induction, and WUPyV with a functional variant in MUC1, previously associated with risk for gastric cancer. These results provide insights into the genetic control of a family of very prevalent human viruses, highlighting genes and pathways that play a modulating role in human humoral immunity.

14,249 European ancestry antibody-positive cases, up to 1,154 European ancestry antibody-negative controls

Chapter III

Study Statistics

Key metrics and study information

15403
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K., Switzerland
Recruitment Country
Chapter IV

AI-Generated Summary

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