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饮食炎症指数与HIV免疫无应答者的肠道通透性或全身炎症生物标志物无关。

The Dietary Inflammatory Index Is Not Associated With Gut Permeability or Biomarkers of Systemic Inflammation in HIV Immunologic Non-responders.

作者信息

Malazogu Fat, Rousseau Rodney K, Shivappa Nitin, Huibner Sanja, Walmsley Sharon L, Kovacs Colin M, Benko Erika, Reinhard Robert J, Rosenes Ron, Hebert James R, Kaul Rupert

机构信息

Departments of Medicine and Immunology, University of Toronto, Toronto, ON, Canada.

Cancer Prevention and Control Program, University of South Carolina, Columbia, SC, United States.

出版信息

Front Nutr. 2021 Nov 22;8:736816. doi: 10.3389/fnut.2021.736816. eCollection 2021.

Abstract

Immunologic non-responders (INRs) are a subset of individuals living with HIV who have suboptimal blood CD4+ T cell recovery despite effective antiretroviral therapy (ART). They are at an increased risk of serious non-AIDS co-morbidities and death, and demonstrate enhanced systemic immune activation. In other populations diet has been correlated with markers of systemic inflammation through the Diet Inflammatory Index (DII), but this association has not been studied in persons living with HIV (PLWH). Blood was collected from 28 INR PLWH with a blood CD4+ T cell count <350/μL despite ≥2 years of effective ART. Participants completed a Canadian Diet History Questionnaire, and their responses were used to calculate the DII. Plasma inflammatory markers (IFNγ, TNF, IL-6, sVCAM, D-dimer, sCD14 and CRP) were assayed by ELISA, cellular immune activation (HLA-DR and CD38 on CD4+ and CD8+ T cells) was quantified using flow cytometry, and small bowel permeability assessed by calculation of the urine LacMan ratio after drinking a mix of lactulose and mannitol. Participants were a median age of 57 years, had been on effective ART for 15 years, and the median DII was -1.91 (range of -3.78 to +2.23). No correlation was observed between DII and plasma markers of inflammation, levels of T cell activation, gut permeability, or the biomarker of bacterial translocation sCD14. Self-reported alcohol intake, a potential confounder of the relationship between diet and inflammatory biomarkers, was also not associated with systemic inflammation or gut permeability. Our findings suggest that other mechanisms, rather than diet, are likely to be the major driver of systemic inflammation in INR individuals.

摘要

免疫无应答者(INR)是感染艾滋病毒者中的一个亚组,尽管接受了有效的抗逆转录病毒疗法(ART),但其血液中CD4 + T细胞恢复情况仍不理想。他们发生严重非艾滋病合并症和死亡的风险增加,并表现出全身免疫激活增强。在其他人群中,饮食通过饮食炎症指数(DII)与全身炎症标志物相关,但这种关联尚未在艾滋病毒感染者(PLWH)中进行研究。从28名INR PLWH中采集血液,尽管他们接受了≥2年的有效ART,但血液中CD4 + T细胞计数<350/μL。参与者完成了一份加拿大饮食历史问卷,并根据他们的回答计算DII。通过ELISA测定血浆炎症标志物(IFNγ、TNF、IL-6、sVCAM、D-二聚体、sCD14和CRP),使用流式细胞术定量细胞免疫激活(CD4 +和CD8 + T细胞上的HLA-DR和CD38),并在饮用乳果糖和甘露醇混合物后通过计算尿液乳糖/甘露醇比值评估小肠通透性。参与者的年龄中位数为57岁,接受有效ART治疗15年,DII中位数为-1.91(范围为-3.78至+2.23)。未观察到DII与血浆炎症标志物、T细胞激活水平、肠道通透性或细菌易位生物标志物sCD14之间存在相关性。自我报告的酒精摄入量作为饮食与炎症生物标志物之间关系的潜在混杂因素,也与全身炎症或肠道通透性无关。我们的研究结果表明,其他机制而非饮食可能是INR个体全身炎症的主要驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/907a/8646029/1034bc22c5e9/fnut-08-736816-g0001.jpg

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