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Protective effect of HLA‐B57 on HCV genotype 2 infection in a West African population

Identifieur interne : 000830 ( Istex/Corpus ); précédent : 000829; suivant : 000831

Protective effect of HLA‐B57 on HCV genotype 2 infection in a West African population

Auteurs : Wing Chia-Ming Chuang ; Francis Sarkodie ; Colin J. Brown ; Shirley Owusu-Ofori ; Juliette Brown ; Chengyao Li ; Cristina Navarrete ; Paul Klenerman ; Jean-Pierre Allain

Source :

RBID : ISTEX:95373D3160E2A7717E344A8120A43D3C167CE4F4

English descriptors

Abstract

Recovery from Hepatitis C virus (HCV) infection is considered infrequent (<20%) in western populations but reaches 50% in West Africa where genotype 2 infection is predominant. To investigate the role of cellular immune responses and host genetics in this phenomenon, samples from 104 Ghanaian blood donors reactive with anti‐HCV assays were collected between 2000 and 2005. HCV antibody was confirmed by Western blot using genotype 2 recombinant core, E2 and NS3 proteins. Viral load and genotype were determined. Samples were stratified into 37 chronic, 35 recovered infections and 32 false positive. Eighty‐one percentage of subjects with chronic infection (RNA positive) carried genotype 2 HCV. Cellular immune response was investigated in 35 frozen peripheral blood mononuclear cell (PBMC) samples suitable for interferon‐gamma ELISPOT assay. Twelve out of 24 confirmed recovered, 1 out of 5 chronically infected and none of the 6 false‐positive controls reacted to recombinant proteins. HLA‐A, ‐B and ‐DR types were determined by DNA methodology. HLA‐B*57 was significantly more frequent in the group which had recovered from HCV infection compared with chronically infected subjects (P = 0.0053, OR = 8.02). In conclusion, it is hypothesized that the dominance of genotype 2 HCV strains may be an important factor explaining the high rate of recovery from HCV infections in Ghana via an efficient contribution of HLA‐B*57 which is relatively frequent in the population. J. Med. Virol. 79: 724–733, 2007. © 2007 Wiley‐Liss, Inc.

Url:
DOI: 10.1002/jmv.20848

Links to Exploration step

ISTEX:95373D3160E2A7717E344A8120A43D3C167CE4F4

Le document en format XML

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<div type="abstract" xml:lang="en">Recovery from Hepatitis C virus (HCV) infection is considered infrequent (<20%) in western populations but reaches 50% in West Africa where genotype 2 infection is predominant. To investigate the role of cellular immune responses and host genetics in this phenomenon, samples from 104 Ghanaian blood donors reactive with anti‐HCV assays were collected between 2000 and 2005. HCV antibody was confirmed by Western blot using genotype 2 recombinant core, E2 and NS3 proteins. Viral load and genotype were determined. Samples were stratified into 37 chronic, 35 recovered infections and 32 false positive. Eighty‐one percentage of subjects with chronic infection (RNA positive) carried genotype 2 HCV. Cellular immune response was investigated in 35 frozen peripheral blood mononuclear cell (PBMC) samples suitable for interferon‐gamma ELISPOT assay. Twelve out of 24 confirmed recovered, 1 out of 5 chronically infected and none of the 6 false‐positive controls reacted to recombinant proteins. HLA‐A, ‐B and ‐DR types were determined by DNA methodology. HLA‐B*57 was significantly more frequent in the group which had recovered from HCV infection compared with chronically infected subjects (P = 0.0053, OR = 8.02). In conclusion, it is hypothesized that the dominance of genotype 2 HCV strains may be an important factor explaining the high rate of recovery from HCV infections in Ghana via an efficient contribution of HLA‐B*57 which is relatively frequent in the population. J. Med. Virol. 79: 724–733, 2007. © 2007 Wiley‐Liss, Inc.</div>
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   |étape=   Corpus
   |type=    RBID
   |clé=     ISTEX:95373D3160E2A7717E344A8120A43D3C167CE4F4
   |texte=   Protective effect of HLA‐B57 on HCV genotype 2 infection in a West African population
}}

Wicri

This area was generated with Dilib version V0.6.31.
Data generation: Tue Nov 7 18:07:38 2017. Site generation: Tue Mar 5 15:01:57 2024