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1.
Braz J Infect Dis ; 7(4): 236-40, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-14533983

RESUMO

Entry of human immunodeficiency type 1 virus (HIV-1) into target cells requires both CD(4)and one of the chemokine receptors. Viruses predominantly use one, or occasionally both, of the major co-receptors CCR5 and CXCR4, although other receptors, including CCR2B and CCR3, function as minor co-receptors. A 32-nucleotide deletion (D32) within the b-chemokine receptor 5 gene (CCR5) has been described in subjects who remain uninfected despite extensive exposition to HIV-1. The heterozygous genotype delays disease progression. This allele is common among Caucasians, but has not been found in people of African or Asian ancestry. A more common transition involving a valine to isoleucine switch in transmembrane domain I of CCR2B (64I), with unknown functional consequences, was found to delay disease progression but not to reduce infection risk. As the Brazilian population consists of a mixture of several ethnic groups, we decided to examine the genotype frequency of these polymorphisms in this country. There were 11.5% CCR5 heterozygotes among the HIV-1 infected population and 12.5% among uninfected individuals, similar to data from North America and Western Europe. The prevalence of CCR2-64I homozygotes and heterozygotes was 0.06 and 15.2%, respectively, also similar to what is known for North America and Western Europe.


Assuntos
Infecções por HIV/genética , HIV-1/genética , Polimorfismo Genético/genética , Receptores CCR5/genética , Receptores de Quimiocinas/genética , Brasil , Estudos Transversais , Feminino , Marcadores Genéticos , Genótipo , Heterozigoto , Homozigoto , Humanos , Masculino , Reação em Cadeia da Polimerase , Prevalência , Receptores CCR2
2.
Braz. j. infect. dis ; Braz. j. infect. dis;7(4): 236-240, Aug. 2003. ilus, tab
Artigo em Inglês | LILACS | ID: lil-351502

RESUMO

Entry of human immunodeficiency type 1 virus (HIV-1) into target cells requires both CD4and one of the chemokine receptors. Viruses predominantly use one, or occasionally both, of the major co-receptors CCR5 and CXCR4, although other receptors, including CCR2B and CCR3, function as minor co-receptors. A 32-nucleotide deletion (delta32) within the beta-chemokine receptor 5 gene (CCR5) has been described in subjects who remain uninfected despite extensive exposition to HIV-1. The heterozygous genotype delays disease progression. This allele is common among Caucasians, but has not been found in people of African or Asian ancestry. A more common transition involving a valine to isoleucine switch in transmembrane domain I of CCR2B (64I), with unknown functional consequences, was found to delay disease progression but not to reduce infection risk. As the Brazilian population consists of a mixture of several ethnic groups, we decided to examine the genotype frequency of these polymorphisms in this country. There were 11.5 percent CCR5 heterozygotes among the HIV-1 infected population and 12.5 percent among uninfected individuals, similar to data from North America and Western Europe. The prevalence of CCR2-64I homozygotes and heterozygotes was 0.06 and 15.2 percent, respectively, also similar to what is known for North America and Western Europe


Assuntos
Humanos , Masculino , Feminino , Infecções por HIV , HIV-1 , Polimorfismo Genético , Receptores de Quimiocinas , Estudos Transversais , Genótipo , Heterozigoto , Reação em Cadeia da Polimerase , Prevalência
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