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APOBEC3G mRNA expression in exposed seronegative and early stage HIV infected individuals decreases with removal of exposure and with disease progression

机译:暴露的血清阴性和早期感染HIV的个体中APOBEC3G mRNA表达随着暴露的去除和疾病进展而降低

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Background APOBEC3G is an antiretroviral factor that acts by inducing G to A mutations. In this study, we examined the expression of APOBEC3G in uninfected HIV-1 exposed individuals at the time of their partner's diagnosis and one year later. We then compared this expression with that of infected individuals at different disease stages. APOBEC3G mRNA was measured in PBMCs from three groups: healthy controls with no known risk factor to HIV infection (n = 26), exposed uninfected individuals who had unprotected sex with their HIV+ partners for at least 3 months (n = 37), and HIV infected patients at various disease stages (n = 45), including 8 patients with low HIV viral loads < 10,000 copies/mL (LVL) for at least 3 years. Additionally, we obtained sequences from the env, gag, pol, nef, vif and the LTR of the patients' virus. Results Exposed uninfected individuals expressed higher APOBEC3G than healthy controls (3.86 vs. 1.69 relative expression units), and their expression significantly decreased after a year from the HIV diagnosis and subsequent treatment of their partners. Infected individuals showed a positive correlation (Rho = 0.57, p = 0.00006) of APOBEC3G expression with CD4+ T cell count, and a negative correlation with HIV viremia (Rho = -0.54, p = 0.00004). The percentage of G to A mutations had a positive correlation (Rho = 0.43, p = 0.0226) with APOBEC3G expression, and it was higher in LVL individuals than in the other patients (IQR 8.27 to 9.64 vs. 7.06 to 8.1, p = 0.0084). Out of 8 LVLs, 3 had hypermutations, and 4 had premature stop codons only in viral vif. Conclusion The results suggest that exposure to HIV may trigger APOBEC3G expression in PBMCs, in the absence of infection. Additionally, cessation of exposure or advanced disease is associated with decreased APOBEC3G expression.
机译:背景APOBEC3G是一种抗逆转录病毒因子,可通过诱导G到A突变发挥作用。在这项研究中,我们检查了伴侣诊断时和一年后未感染HIV-1的个体中APOBEC3G的表达。然后,我们将该表达与处于不同疾病阶段的受感染个体的表达进行了比较。在三组PBMC中测量了APOBEC3G mRNA:健康对照组,没有已知的HIV感染危险因素(n = 26),暴露的未感染者与HIV +伴侣进行了至少3个月的无保护性行为(n = 37),以及HIV处于不同疾病阶段(n = 45)的感染患者,包括8位HIV病毒载量低于10,000份/ mL(LVL)的患者,至少持续3年。另外,我们从env,gag,pol,nef,vif和患者病毒的LTR获得了序列。结果暴露的未感染个体表达的APOBEC3G高于健康对照组(3.86比1.69相对表达单位),并且经过HIV诊断和其伴侣的一年治疗后,其表达明显下降。受感染的个体显示APOBEC3G表达与CD4 + T细胞计数呈正相关(Rho = 0.57,p = 0.00006),而与HIV病毒血症呈负相关(Rho = -0.54,p = 0.00004)。 G到A突变的百分比与APOBEC3G表达呈正相关(Rho = 0.43,p = 0.0226),LVL个体中的百分比高于其他患者(IQR 8.27至9.64对7.06至8.1,p = 0.0084 )。在8个LVL中,只有3个具有超突变,而4个仅在病毒vif中具有过早的终止密码子。结论结果表明,在没有感染的情况下,暴露于HIV可能会触发PBMC中APOBEC3G的表达。另外,停止接触或疾病晚期与APOBEC3G表达降低有关。

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