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尼日利亚HIV感染者中Bf S基因频率。

Bf S gene frequency in Nigerians with HIV infection.

作者信息

Uko G P, Dawkins R L, Mohammed I, Kay P H, Christiansen F T, Nasidi A, Bajani M

机构信息

Department of Immunology, University of Maiduguri Teaching Hospital, Nigeria.

出版信息

Dis Markers. 1991 Nov-Dec;9(6):333-8.

PMID:1823312
Abstract

Complement immunogenetic susceptibility to human immunodeficiency virus (HIV) infection was examined in 40 Nigerians with serological and/or clinical evidence of the infection. A mild increase in C4A null alleles (C4AQO) frequency was observed in the patient group compared to a group of healthy subjects (25 per cent vs 17 per cent) but overall the HIV infected and the reference groups did not differ significantly in the frequency of alleles of C4A or C4B. In contrast, properdin factor B (Bf) S gene frequency was significantly higher in the patients with HIV infection (p less than 0.025). There was a concomitant decrease in Bf F allele and gene frequencies (p less than 0.01, and p less than 0.05), respectively. Furthermore, blank Bf allotypes due to excessive complement consumption were detected in two asymptomatic patients. These findings suggest that Major Histocompatibility Complex (MHC) located complement genes may be important HIV infection. In particular Bf S gene or even C4AQO alleles may be permissive or influence outcome of infection with HIV.

摘要

对40名有人类免疫缺陷病毒(HIV)感染血清学和/或临床证据的尼日利亚人进行了补体免疫遗传学易感性研究。与一组健康受试者相比,患者组中C4A无效等位基因(C4AQO)频率略有增加(25%对17%),但总体而言,HIV感染者和参照组在C4A或C4B等位基因频率上无显著差异。相比之下,备解素因子B(Bf)S基因频率在HIV感染患者中显著更高(p<0.025)。Bf F等位基因和基因频率分别随之降低(p<0.01和p<0.05)。此外,在两名无症状患者中检测到由于补体过度消耗导致的空白Bf同种异型。这些发现表明,位于主要组织相容性复合体(MHC)的补体基因可能对HIV感染很重要。特别是Bf S基因甚至C4AQO等位基因可能允许HIV感染或影响其感染结果。

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