Heterosexual transmission of human immunodeficiency virus type 1 from transfusion recipients to their sex partners.

T R O'Brien, M P Busch, E Donegan, J W Ward, L Wong, S M Samson, H A Perkins, R Altman, R L Stoneburner, S D Holmberg
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Abstract

Using lookback procedures and other methods, we identified and then prospectively followed human immunodeficiency virus type 1 (HIV-1)-infected transfusion recipients and their sex partners to determine AIDS incidence and risks of heterosexual transmission of HIV-1. At enrollment, 7 of 32 (21.9%) female partners of male recipients were themselves infected with HIV-1, as compared with none of 14 male partners of female recipients (p = 0.08). No additional episodes of transmission were observed. The prevalence of advanced immunodeficiency at enrollment was similar in male and female recipients. Male recipients with advanced immunodeficiency (CD4+ lymphocyte count < or = 0.20 x 10(9)/L or a history of clinical AIDS) at enrollment were more likely to have infected their female partners (odds ratio = 7.9; p = 0.03) than men with neither condition. Similarly, AIDS-free survival, as estimated by the product-limit method, was lower among male transmitters than among male nontransmitters (p = 0.01). Transmission was not associated with frequency of unprotected vaginal intercourse. Our data suggest that HIV-1-infected men who develop immunodeficiency rapidly are more likely to infect their sex partners and that the greater efficiency of male-to-female HIV-1 transmission is not explained by a greater number of sexual contacts or more advanced immunodeficiency in index subjects.

人类免疫缺陷病毒1型从输血者到其性伴侣的异性传播。
采用回溯程序和其他方法,我们确定并前瞻性跟踪人类免疫缺陷病毒1型(HIV-1)感染输血者及其性伴侣,以确定艾滋病发病率和异性传播HIV-1的风险。在入组时,32名男性接受者的女性伴侣中有7名(21.9%)本身感染了HIV-1,而14名女性接受者的男性伴侣中没有感染HIV-1 (p = 0.08)。未观察到其他传播事件。在入组时,晚期免疫缺陷的患病率在男性和女性接受者中相似。入组时具有晚期免疫缺陷(CD4+淋巴细胞计数<或= 0.20 x 10(9)/L或有临床艾滋病史)的男性受体更有可能感染其女性伴侣(优势比= 7.9;P = 0.03)。同样,用产品限法估计,男性传递者的无艾滋病生存率低于男性非传递者(p = 0.01)。传播与无保护阴道性交的频率无关。我们的数据表明,HIV-1感染的男性迅速发展为免疫缺陷者更有可能感染他们的性伴侣,男性向女性传播HIV-1的效率更高,并不能用更多的性接触或更严重的免疫缺陷来解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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