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"Telling my husband I have HIV is too heavy to come out of my mouth": pregnant women's disclosure experiences and support needs following antenatal HIV testing in eastern Uganda.“告诉我丈夫我感染了艾滋病毒,这太沉重了,难以启齿”:乌干达东部孕妇在接受产前 HIV 检测后,讲述自己的披露经历和支持需求。
J Int AIDS Soc. 2012;15(2):17429. doi: 17429.
2
Association of bactericidal activity of genital tract secretions with Escherichia coli colonization in pregnancy.生殖道分泌物杀菌活性与妊娠期间大肠埃希菌定植的关系。
Am J Obstet Gynecol. 2012 Oct;207(4):297.e1-8. doi: 10.1016/j.ajog.2012.07.025. Epub 2012 Jul 26.
3
Altered biomarkers of mucosal immunity and reduced vaginal Lactobacillus concentrations in sexually active female adolescents.性活跃的女青少年中,黏膜免疫的生物标志物改变和阴道内乳杆菌浓度降低。
PLoS One. 2012;7(7):e40415. doi: 10.1371/journal.pone.0040415. Epub 2012 Jul 10.
4
In vitro anti-HIV-1 activity in cervicovaginal secretions from pregnant and nonpregnant women.孕妇和非孕妇宫颈阴道分泌物中的抗 HIV-1 活性。
Am J Obstet Gynecol. 2012 Jul;207(1):65.e1-10. doi: 10.1016/j.ajog.2012.04.029. Epub 2012 Apr 30.
5
Selective impact of HIV disease progression on the innate immune system in the human female reproductive tract.HIV 疾病进展对人类女性生殖道固有免疫系统的选择性影响。
PLoS One. 2012;7(6):e38100. doi: 10.1371/journal.pone.0038100. Epub 2012 Jun 4.
6
Trauma equals danger--damage control by the immune system.创伤等于危险--免疫系统的损伤控制。
J Leukoc Biol. 2012 Sep;92(3):539-51. doi: 10.1189/jlb.0212072. Epub 2012 May 31.
7
Adherence to HIV post-exposure prophylaxis in victims of sexual assault: a systematic review and meta-analysis.艾滋病病毒暴露后预防用药在性侵犯受害者中的依从性:系统评价和荟萃分析。
Sex Transm Infect. 2012 Aug;88(5):335-41. doi: 10.1136/sextrans-2011-050371. Epub 2012 Feb 13.
8
Quality and quantity: mucosal CD4+ T cells and HIV susceptibility.质量与数量:黏膜 CD4+T 细胞与 HIV 易感性。
Curr Opin HIV AIDS. 2012 Mar;7(2):195-202. doi: 10.1097/COH.0b013e3283504941.
9
CCR5 expression is elevated on endocervical CD4+ T cells in healthy postmenopausal women.健康绝经后妇女的宫颈内 CD4+T 细胞上 CCR5 的表达增加。
J Acquir Immune Defic Syndr. 2012 Mar 1;59(3):221-8. doi: 10.1097/QAI.0b013e31823fd215.
10
Characterization of a human cervical CD4+ T cell subset coexpressing multiple markers of HIV susceptibility.鉴定人宫颈 CD4+T 细胞亚群,该亚群共表达多种 HIV 易感性标志物。
J Immunol. 2011 Dec 1;187(11):6032-42. doi: 10.4049/jimmunol.1101836. Epub 2011 Nov 2.

生殖道创伤的免疫生物学:性侵犯或生殖道切割后女性获得性 HIV 的内分泌调节。

Immunobiology of genital tract trauma: endocrine regulation of HIV acquisition in women following sexual assault or genital tract mutilation.

机构信息

Department of Epidemiology and Biostatistics, The George Washington University, Washington, DC 20037, USA.

出版信息

Am J Reprod Immunol. 2013 Feb;69 Suppl 1(Suppl 1):51-60. doi: 10.1111/aji.12027. Epub 2012 Oct 4.

DOI:10.1111/aji.12027
PMID:23034063
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3566368/
Abstract

Studies on HIV acquisition and transmission in women exposed to sexual trauma throughout their life cycle are lacking, but some findings suggest that rates of HIV acquisition through coercive sex are significantly higher than that seen in consensual sex. Sexual trauma can also occur as a result of female genital mutilation, which makes sex extremely painful and can cause increased abrasions, lacerations, and inflammation, which enhances the risk of HIV acquisition. This review presents an overview of the immune system in the human female reproductive tract (FRT) from adolescence, through puberty to pregnancy and menopause. What is clear is that the foundation of information on immune protection in the FRT throughout the life cycle of women is extremely limited and at some stages such as adolescence and menopause are grossly lacking. Against this backdrop, forced or coercive sexual intercourse as well as genital mutilation further complicates our understanding of the biological risk factors that can result in transmission of HIV and other sexually transmitted infections.

摘要

针对一生中都遭受过性创伤的女性的 HIV 获得和传播的研究很少,但有一些研究结果表明,通过强迫性行为获得 HIV 的比率明显高于自愿性行为。性创伤也可能是由于女性割礼造成的,这会使性行为极其痛苦,并导致更多的擦伤、撕裂和炎症,从而增加 HIV 感染的风险。这篇综述概述了人类女性生殖道(FRT)从青春期到怀孕和更年期的免疫系统。很明显,女性一生中 FRT 免疫保护信息的基础极其有限,在某些阶段,如青春期和更年期,更是严重缺乏。在这种背景下,强迫或强制性交以及割礼进一步使我们难以理解可能导致 HIV 和其他性传播感染传播的生物学风险因素。