ABSTRACT
Hepatitis B virus (HBV) has seven genotypes, A to G. Previous studies have shown that genotype C is the most prevalent strain in chronic HBV carriers in East Asia. This study was undertaken to investigate the epidemiology of HBV genotypes among Japanese patients who are coinfected with human immunodeficiency virus type 1 (HIV-1). The sequences of the complete hepatitis B surface antifen (HBsAg) genes were obtained from 18 coinfected Japanese patients. Among the 18 patients, 12 of 13 men who had sex with men (MSM) had genotype A (92%), whereas only one of five heterosexual or hemophiliac patients had genotype A. The predominance of genotype A HBV in MSM showed a striking contrast to the current genotype prevalence in the Japanese population. Owing to the recent decrease in the rate of vertical transmission in Japan, the role of sexual behavior in the transmission of HBV cannot be overestimated. Thus, the relative proportion of genotype A may gradually increase in Japan.
Subject(s)
Genes, Viral , HIV Infections/complications , HIV-1 , Hepatitis B virus/genetics , Hepatitis B, Chronic/complications , Adult , Base Sequence , Female , Genotype , HIV Infections/virology , Hepatitis B Surface Antigens/genetics , Hepatitis B virus/classification , Hepatitis B, Chronic/epidemiology , Heterosexuality , Homosexuality, Male , Humans , Japan/epidemiology , Male , Middle Aged , Molecular Sequence Data , Risk FactorsSubject(s)
AIDS-Related Opportunistic Infections/drug therapy , Antifungal Agents/adverse effects , Cryptococcosis/drug therapy , Desensitization, Immunologic , Fluconazole/adverse effects , Lung Diseases, Fungal/drug therapy , AIDS-Related Opportunistic Infections/diagnostic imaging , Cryptococcosis/diagnostic imaging , Drug Hypersensitivity , Humans , Lung Diseases, Fungal/diagnostic imaging , Male , Middle Aged , RadiographyABSTRACT
The emergence of syncytium-inducing (SI) variants of human immunodeficiency virus type 1 (HIV-1) in infected individuals is an indicator of poor prognosis and is often correlated with faster CD4(+) cell depletion and rapid disease progression. Interleukin-4 (IL-4) is a pleiotropic cytokine with various immune-modulating functions including induction of immunoglobulin E (IgE) production in B cells, down-regulation of CCR5 (a coreceptor for HIV-1 non-SI [NSI] strains), and up-regulation of CXCR4 (a coreceptor for HIV-1 SI variants). Here we show that homozygosity of a polymorphism in the IL-4 promoter region, IL-4 -589T, is correlated with increased rates of SI variant acquisition in HIV-1-infected individuals in Japan. This mutation was also shown to be associated with elevated serum IgE levels in HIV-1-infected individuals, especially in those at advanced stages of disease. In contrast, neither a triallele polymorphism in IL-10, another Th2 cytokine, nor a biallele polymorphism in the RANTES promoter affected acquisition of the SI phenotype. This finding suggested that IL-4-589T increases IL-4 production in the human body and thus accelerates the phenotypic switch of HIV-1 from NSI to SI and possibly disease progression of AIDS.
