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Evaluating the Impact of Functional Genetic Variation on HIV-1 Control

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  • معلومة اضافية
    • Contributors:
      Swiss National Science Foundation; Swiss HIV Cohort Study; Harvard University (Estados Unidos); University of California, San Francisco (Estados Unidos); Unión Europea. Comisión Europea. 7 Programa Marco; Red de Investigación Cooperativa en Investigación en Sida (España); NIH - National Institute of Allergy and Infectious Diseases (NIAID) (Estados Unidos); NIH - National Cancer Institute (NCI) (Estados Unidos); NIH - National Institute on Drug Abuse (NIDA) (Estados Unidos); NIH - National Institute of Mental Health (NIMH) (Estados Unidos); NIH - National Heart, Lung, and Blood Institute (NHLBI) (Estados Unidos); NIH - National Institute on Deafness and Communication Disorders (NIDCD) (Estados Unidos)
    • بيانات النشر:
      Oxford University Press
    • الموضوع:
      2017
    • Collection:
      REPISALUD (REPositorio Institucional en SALUD del Instituto de Salud Carlos III - ISCIII)
    • نبذة مختصرة :
      Background. Previous genetic association studies of human immunodeficiency virus-1 (HIV-1) progression have focused on common human genetic variation ascertained through genome-wide genotyping. Methods. We sought to systematically assess the full spectrum of functional variation in protein coding gene regions on HIV-1 progression through exome sequencing of 1327 individuals. Genetic variants were tested individually and in aggregate across genes and gene sets for an influence on HIV-1 viral load. Results. Multiple single variants within the major histocompatibility complex (MHC) region were observed to be strongly associated with HIV-1 outcome, consistent with the known impact of classical HLA alleles. However, no single variant or gene located outside of the MHC region was significantly associated with HIV progression. Set-based association testing focusing on genes identified as being essential for HIV replication in genome-wide small interfering RNA (siRNA) and clustered regularly interspaced short palindromic repeats (CRISPR) studies did not reveal any novel associations. Conclusions. These results suggest that exonic variants with large effect sizes are unlikely to have a major contribution to host control of HIV infection. ; This study has been financed in part within the framework of the Swiss HIV Cohort Study (www.shcs.ch) project #651 and supported by the Swiss National Science Foundation (www.snf.ch) grant #148522 (J.F.). The International HIV Controllers Study was made possible through a generous donation from the Mark and Lisa Schwartz Foundation and a subsequent award from the Collaboration for AIDS Vaccine Discovery of the Bill and Melinda Gates Foundation (www.cavd.org). This work was also supported in part by the Harvard University Center for AIDS Research (cfar.globalhealth.harvard.edu) grant P-30-AI060354; University of California San Francisco (UCSF) Center for AIDS Research (cfar.ucsf.edu) grant P-30 AI27763; UCSF Clinical and Translational Science Institute (https://ctsi.ucsf.edu) grant UL1 ...
    • ISSN:
      1537-6613
    • Relation:
      https://doi.org/10.1093/infdis/jix470; info:eu-repo/grantAgreement/EC/FP7/260694/EU; info:eu-repo/grantAgreement/ES/RD06/006; info:eu-repo/grantAgreement/ES/RD12/0017/0018; info:eu-repo/grantAgreement/ES/RD16CIII/0002/0006; J Infect Dis. 2017 Nov 27;216(9):1063-1069; http://hdl.handle.net/20.500.12105/14103; The Journal of Infectious Diseases
    • الرقم المعرف:
      10.1093/infdis/jix470
    • Rights:
      http://creativecommons.org/licenses/by/4.0/ ; Atribución 4.0 Internacional ; open access
    • الرقم المعرف:
      edsbas.128E6333