Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer
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Published:2021-10-12
Issue:1
Volume:12
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Ferreiro-Iglesias AidaORCID, McKay James D., Brenner NicoleORCID, Virani ShamaORCID, Lesseur CorinaORCID, Gaborieau Valerie, Ness Andy R., Hung Rayjean J.ORCID, Liu Geoffrey, Diergaarde Brenda, Olshan Andrew F., Hayes NeilORCID, Weissler Mark C., Schroeder Lea, Bender Noemi, Pawlita MichaelORCID, Thomas Steve, Pring Miranda, Dudding TomORCID, Kanterewicz Beatriz, Ferris Robert, Thomas Sera, Brhane Yonathan, Díez-Obrero Virginia, Milojevic MajaORCID, Smith-Byrne KarlORCID, Mariosa DanielaORCID, Johansson Mattias J.ORCID, Herrero Rolando, Boccia Stefania, Cadoni Gabriella, Lacko MartinORCID, Holcátová Ivana, Ahrens Wolfgang, Lagiou Pagona, Lagiou Areti, Polesel JerryORCID, Simonato Lorenzo, Merletti Franco, Healy Claire M., Hansen Bo T., Nygård Mari, Conway David I., Wright Sylvia, Macfarlane Tatiana V., Robinson MaxORCID, Alemany Laia, Agudo Antonio, Znaor ArianaORCID, Amos Christopher I., Waterboer Tim, Brennan PaulORCID
Abstract
AbstractAlthough several oropharyngeal cancer (OPC) susceptibility loci have been identified, most previous studies lacked detailed information on human papillomavirus (HPV) status. We conduct a genome-wide analysis by HPV16 serology status in 4,002 oral cancer cases (OPC and oral cavity cancer (OCC)) and 5,256 controls. We detect four susceptibility loci pointing to a distinct genetic predisposition by HPV status. Our most notable finding in the HLA region, that is now confirmed to be specific of HPV(+)OPC risk, reveal two independent loci with strong protective effects, one refining the previously reported HLA class II haplotype association. Antibody levels against HPV16 viral proteins strongly implicate the protective HLA variants as major determinants of humoral response against L1 capsid protein or E6 oncoprotein suggesting a natural immune response against HPV(+)OPC promoted by HLA variants. This indicates that therapeutic vaccines that target E6 and attenuate viral response after established HPV infections might protect against HPV(+)OPC.
Funder
U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference54 articles.
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