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Treatment with Commonly Used Antiretroviral Drugs Induces a Type I/III Interferon Signature in the Gut in the Absence of HIV Infection

机译:用常用的抗逆转录病毒药物治疗在没有艾滋病毒感染的情况下诱导肠道中的I / III干扰素签名

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摘要

Summary: Tenofovir disoproxil fumarate (TDF) and emtricitabine (FTC) are used for HIV treatment and prevention. Previously, we found that topical rectal tenofovir gel caused immunological changes in the mucosa. Here, we assess the effect of oral TDF/FTC in three HIV pre-exposure prophylaxis trials, two with gastrointestinal and one with cervicovaginal biopsies. TDF/FTC induces type I/III interferon-related (IFN I/III) genes in the gastrointestinal tract, but not blood, with strong correlations between the two independent rectal biopsy groups (Spearman r = 0.91) and between the rectum and duodenum (r = 0.81). Gene set testing also indicates stimulation of the type I/III pathways in the ectocervix and of cellular proliferation in the duodenum. mRNA sequencing, digital droplet PCR, proteomics, and immunofluorescence confirm IFN I/III pathway stimulation in the gastrointestinal tract. Thus, oral TDF/FTC stimulates an IFN I/III signature throughout the gut, which could increase antiviral efficacy but also cause chronic immune activation in HIV prevention and treatment settings.
机译:发明内容:替诺福韦解毒富马酸核苷酸(TDF)和Emtrickabine(FTC)用于艾滋病毒治疗和预防。以前,我们发现局部直肠藤酰胶凝胶导致粘膜中的免疫变化。在这里,我们评估口服TDF / FTC在三个艾滋病毒预曝光预防试验中的影响,其中两个用胃肠道和宫颈病变活组织检查。 TDF / FTC在胃肠道中诱导I / III干扰素相关(IFN I / III)基因,但不是血液,两种独立直肠活检基(Spearman R = 0.91)和直肠和十二指肠之间的强关系r = 0.81)。基因设定测试还表明,在十二指肠中刺激了异细胞和细胞增殖中的I / III型途径。 mRNA测序,数字液滴PCR,蛋白质组学和免疫荧光确认IFN I / III途径在胃肠道中刺激。因此,口服TDF / FTC在整个肠道中刺激IFN I / III签名,这可以提高抗病毒功效,而且导致艾滋病毒预防和治疗环境中的慢性免疫激活。

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