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Relevance of Interleukin-6 and D-Dimer for Serious Non-AIDS Morbidity and Death among HIV-Positive Adults on Suppressive Antiretroviral Therapy.白细胞介素-6和D-二聚体与接受抑制性抗逆转录病毒治疗的HIV阳性成年人严重非艾滋病发病率和死亡率的相关性。
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A phase 2 randomized, double-blind, placebo-controlled study of the safety and efficacy of talactoferrin in patients with severe sepsis.一项关于乳铁蛋白在严重脓毒症患者中的安全性和疗效的 2 期随机、双盲、安慰剂对照研究。
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Plasma levels of soluble CD14 independently predict mortality in HIV infection.血浆可溶性 CD14 水平可独立预测 HIV 感染患者的死亡率。
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重组人乳铁蛋白对接受抗逆转录病毒治疗的人类免疫缺陷病毒感染者免疫激活和肠道微生物组的影响。

The Effects of Recombinant Human Lactoferrin on Immune Activation and the Intestinal Microbiome Among Persons Living with Human Immunodeficiency Virus and Receiving Antiretroviral Therapy.

机构信息

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.

Division of Infectious Diseases, Department of Medicine, University of Minnesota.

出版信息

J Infect Dis. 2019 May 24;219(12):1963-1968. doi: 10.1093/infdis/jiz042.

DOI:10.1093/infdis/jiz042
PMID:30721997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6784498/
Abstract

Lactoferrin modulates mucosal immunity and targets mechanisms contributing to inflammation during human immunodeficiency virus disease. A randomized placebo-controlled crossover clinical trial of recombinant human (rh) lactoferrin was conducted among 54 human immunodeficiency virus-infected participants with viral suppression. Outcomes were tolerability, inflammatory, and immunologic measures, and the intestinal microbiome. The median age was 51 years, and the median CD4+ cell count was 651/µL. Adherence and adverse events did not differ between rh-lactoferrin and placebo. There was no significant effect on plasma interleukin-6 or D-dimer levels, nor on monocyte/T-cell activation, mucosal integrity, or intestinal microbiota diversity. Oral administration of rh-lactoferrin was safe but did not reduce inflammation and immune activation. Clinical Trials Registration: NCT01830595.

摘要

乳铁蛋白调节黏膜免疫,并针对人类免疫缺陷病毒疾病期间导致炎症的机制。在 54 名病毒抑制的人类免疫缺陷病毒感染参与者中,进行了重组人(rh)乳铁蛋白的随机安慰剂对照交叉临床试验。结果是耐受性、炎症和免疫指标以及肠道微生物组。中位年龄为 51 岁,中位 CD4+细胞计数为 651/µL。rh-乳铁蛋白和安慰剂之间的依从性和不良事件没有差异。对血浆白细胞介素 6 或 D-二聚体水平、单核细胞/ T 细胞活化、黏膜完整性或肠道微生物多样性均无显著影响。口服 rh-乳铁蛋白是安全的,但不能减轻炎症和免疫激活。临床试验注册:NCT01830595。