Relation of HLA class I and II supertypes with spontaneous clearance of hepatitis C virus View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-07

AUTHORS

Mark H. Kuniholm, Kathryn Anastos, Andrea Kovacs, Xiaojiang Gao, Darlene Marti, Allesandro Sette, Ruth M. Greenblatt, Marion Peters, Mardge H. Cohen, Howard Minkoff, Stephen J. Gange, Chloe L. Thio, Mary A. Young, Xiaonan Xue, Mary Carrington, Howard D. Strickler

ABSTRACT

Human leukocyte antigen (HLA) genotype has been associated with the probability of spontaneous clearance of hepatitis C virus (HCV). However, no prior studies have examined whether this relationship may be further characterized by grouping HLA alleles according to their supertypes, defined by their binding capacities. There is debate regarding the most appropriate method to define supertypes. Therefore, previously reported HLA supertypes (46 class I and 25 class II) were assessed for their relation with HCV clearance in a population of 758 HCV-seropositive women. Two HLA class II supertypes were significant in multivariable models that included: (i) supertypes with significant or borderline associations with HCV clearance after adjustment for multiple tests, and (ii) individual HLA alleles not part of these supertypes, but associated with HCV clearance in our prior study in this population. Specifically, supertype DRB3 (prevalence ratio (PR)=0.4; P=0.004) was associated with HCV persistence, whereas DR8 (PR=1.8; P=0.01) was associated with HCV clearance. Two individual alleles (B*57:01 and C*01:02) associated with HCV clearance in our prior study became nonsignificant in analysis that included supertypes, whereas B*57:03 (PR=1.9; P=0.008) and DRB1*07:01 (PR=1.7; P=0.005) retained their significance. These data provide epidemiologic support for the significance of HLA supertypes in relation to HCV clearance. More... »

PAGES

330

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/gene.2013.25

DOI

http://dx.doi.org/10.1038/gene.2013.25

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1018637283

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/23636221


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