Correlations of CTLA-4 gene polymorphisms and hepatitis C chronic infection
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
01/11/2013
01/11/2013
2012
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Resumo |
Background: Cytotoxic T lymphocyte-associated factor 4 (CTLA-4) functions as a negative regulator of T cell-mediated immune response. Molecular changes associated to CTLA-4 gene polymorphisms could reduce its ability to suppress and control lymphocyte proliferation. Aims: To evaluate the frequency of CTLA-4 gene polymorphisms in chronic hepatitis C virus (HCV) infected patients and correlate to clinical and histological findings. Methods: We evaluated 112 HCV-infected subjects prospectively selected and 183 healthy controls. Clinical and liver histological data were analysed. - 318C > T, A49G and CT60 CTLA-4 single-nucleotide polymorphisms (SNPs) were studied by PCR-RFLP and AT(n) polymorphism by DNA fragment analysis by capillary electrophoresis in automatic sequencer. Results: Eight AT repetitions in 3' UTR region were more frequent in HCV-infected subjects. We found a positive association of -318C and + 49G with HCV genotype 3 (P = 0.008, OR 9.13, P = 0.004, OR 2.49 respectively) and an inverse association of both alleles with HCV genotype 1 (P = 0.020, OR 0.19, P = 0.002, OR 0.38 respectively). Allele + 49G was also associated to aminotransferases quotients > 3 (qALT, P = 0.034, qAST, P = 0.041). Allele G of CT60 SNP was also associated with qAST > 3 (P = 0.012). Increased number of AT repetitions was positively associated to severe necroinflammatory activity scores in liver biopsies (P = 0.045, OR 4.62). Conclusion: CTLA-4 gene polymorphisms were associated to HCVinfection. Eight AT repetitions were more prevalent in HCV-infected subjects. - 318C and + 49G alleles were associated to genotypes 1 and 3 infections and increased number of AT repetitions in 3' UTR region favoured severe necroinflammatory activity scores in liver biopsies. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [2006/06080-2] |
Identificador |
LIVER INTERNATIONAL, MALDEN, v. 32, n. 5, supl. 1, Part 1, pp. 803-808, MAY, 2012 1478-3223 http://www.producao.usp.br/handle/BDPI/37222 10.1111/j.1478-3231.2011.02694.x |
Idioma(s) |
eng |
Publicador |
WILEY-BLACKWELL MALDEN |
Relação |
LIVER INTERNATIONAL |
Direitos |
closedAccess Copyright WILEY-BLACKWELL |
Palavras-Chave | #CTLA-4 #HEPATITIS C #HEPATITIS C VIRUS GENOTYPE #NECROINFLAMMATORY ACTIVITY SCORE #VIRUS-INFECTION #SUSCEPTIBILITY GENE #DISEASE PROGRESSION #GRAVES-DISEASE #T-CELLS #ASSOCIATION #INTERLEUKIN-10 #AUTOIMMUNITY #POPULATION #EXPRESSION #GASTROENTEROLOGY & HEPATOLOGY |
Tipo |
article original article publishedVersion |