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The mouth: a gateway or a trap for HIV?口腔:是HIV的入口还是陷阱?
AIDS. 2010 Jan 2;24(1):5-16. doi: 10.1097/QAD.0b013e328333525f.
2
Excretion of human immunodeficiency virus type 1 through polarized epithelium by immunoglobulin A.1型人类免疫缺陷病毒通过免疫球蛋白A经极化上皮细胞排泄
J Virol. 2008 Dec;82(23):11526-35. doi: 10.1128/JVI.01111-08. Epub 2008 Oct 1.
3
Rethinking the heterosexual infectivity of HIV-1: a systematic review and meta-analysis.重新审视HIV-1的异性传播感染性:一项系统评价与荟萃分析
Lancet Infect Dis. 2008 Sep;8(9):553-63. doi: 10.1016/S1473-3099(08)70156-7. Epub 2008 Aug 4.
4
Herpes simplex virus downregulates secretory leukocyte protease inhibitor: a novel immune evasion mechanism.单纯疱疹病毒下调分泌型白细胞蛋白酶抑制剂:一种新的免疫逃避机制。
J Virol. 2008 Oct;82(19):9337-44. doi: 10.1128/JVI.00603-08. Epub 2008 Jul 30.
5
Pathogenic mechanisms of B-lymphocyte dysfunction in HIV disease.HIV疾病中B淋巴细胞功能障碍的致病机制。
J Allergy Clin Immunol. 2008 Jul;122(1):12-9; quiz 20-1. doi: 10.1016/j.jaci.2008.04.034. Epub 2008 Jun 10.
6
Nonhuman primate models and the failure of the Merck HIV-1 vaccine in humans.非人灵长类动物模型与默克公司HIV-1疫苗在人体试验中的失败
Nat Med. 2008 Jun;14(6):617-21. doi: 10.1038/nm.f.1759.
7
HIV-neutralizing immunoglobulin A and HIV-specific proliferation are independently associated with reduced HIV acquisition in Kenyan sex workers.在肯尼亚性工作者中,HIV中和免疫球蛋白A和HIV特异性增殖与HIV感染率降低独立相关。
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8
Neutralizing monoclonal antibodies to human immunodeficiency virus type 1 do not inhibit viral transcytosis through mucosal epithelial cells.针对1型人类免疫缺陷病毒的中和单克隆抗体不会抑制病毒通过黏膜上皮细胞的转胞吞作用。
Virology. 2008 Jan 20;370(2):246-54. doi: 10.1016/j.virol.2007.09.006. Epub 2007 Oct 24.
9
Epithelial cells trigger frontline immunoglobulin class switching through a pathway regulated by the inhibitor SLPI.上皮细胞通过由抑制剂SLPI调控的途径触发一线免疫球蛋白类别转换。
Nat Immunol. 2007 Mar;8(3):294-303. doi: 10.1038/ni1434. Epub 2007 Jan 28.
10
Hiv-specific secretory IgA in breast milk of HIV-positive mothers is not associated with protection against HIV transmission among breast-fed infants.HIV阳性母亲母乳中的HIV特异性分泌型IgA与母乳喂养婴儿的HIV传播防护无关。
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HIV 载量、免疫和治疗反应的全身和黏膜差异。

Systemic and mucosal differences in HIV burden, immune, and therapeutic responses.

机构信息

Oral Infection and Immunity Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892-4352, USA.

出版信息

J Acquir Immune Defic Syndr. 2011 Apr 15;56(5):401-11. doi: 10.1097/QAI.0b013e31820cdfdb.

DOI:10.1097/QAI.0b013e31820cdfdb
PMID:21239996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3164950/
Abstract

BACKGROUND

Mucosal tissues represent major targets for HIV transmission but differ in susceptibility and reservoir function by unknown mechanisms.

METHODS

In a cross-sectional study, HIV RNA and infectious virus were compared between oral and genital compartments and blood in HIV-infected women, in association with clinical parameters, copathogens, and putative innate and adaptive HIV inhibitors.

RESULTS

HIV RNA was detectable in 24.5% of women from all 3 compartments, whereas 45% had RNA in only 1 or 2 sites. By comparison, infectious HIV, present in blood of the majority, was rare in mucosal sites. Innate mediators, secretory leukocyte protease inhibitor and thrombospondin, were highest in mucosae. Highly active antiretroviral therapy was associated with an 80% decreased probability of shedding. Multivariate logistic regression models revealed that mucosal HIV RNA was associated with higher plasma RNA, infectious virus, and total mucosal IgA, but not IgG. There was a 37-fold increased probability of detecting RNA in both genital and oral specimens (P = 0.008; P = 0.02, respectively) among women in highest versus lowest IgA tertiles.

CONCLUSIONS

Mucosal sites exhibit distinct characteristics of infectious HIV, viral shedding, and responses to therapy, dependent upon both systemic and local factors. Of the putative innate and adaptive mucosal defense factors examined, only IgA was associated with HIV RNA shedding. However, rather than being protective, there was a striking increase in probability of detectable HIV RNA shedding in women with highest total IgA.

摘要

背景

黏膜组织是 HIV 传播的主要靶标,但通过未知机制,它们在易感性和储库功能方面存在差异。

方法

在一项横断面研究中,比较了 HIV 感染者口腔和生殖器部位与血液中 HIV RNA 和感染性病毒,同时结合临床参数、共病原体以及潜在的先天和适应性 HIV 抑制剂。

结果

所有 3 个部位的女性中,有 24.5%可检测到 HIV RNA,而 45%的女性仅在 1 或 2 个部位有 RNA。相比之下,存在于大多数血液中的感染性 HIV 在黏膜部位很少见。先天介质,如分泌白细胞蛋白酶抑制剂和血栓反应蛋白,在黏膜中含量最高。高效抗逆转录病毒治疗与降低 80%病毒脱落的可能性相关。多变量逻辑回归模型显示,黏膜 HIV RNA 与血浆 RNA、感染性病毒和总黏膜 IgA 水平升高有关,但与 IgG 无关。在 IgA 最高和最低三分位数的女性中,生殖道和口腔标本中均检测到 RNA 的概率分别增加了 37 倍(P = 0.008;P = 0.02)。

结论

黏膜部位具有独特的感染性 HIV、病毒脱落和治疗反应特征,这取决于全身和局部因素。在所检查的潜在先天和适应性黏膜防御因素中,只有 IgA 与 HIV RNA 脱落有关。然而,与保护作用相反,在 IgA 总量最高的女性中,HIV RNA 脱落的检测概率显著增加。