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探讨 HIV 感染中的慢性炎症、免疫代谢和 T 细胞功能障碍。

Examining Chronic Inflammation, Immune Metabolism, and T Cell Dysfunction in HIV Infection.

机构信息

Division of Hematology/Oncology, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

UCLA AIDS Institute and the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.

出版信息

Viruses. 2024 Jan 31;16(2):219. doi: 10.3390/v16020219.

Abstract

Chronic Human Immunodeficiency Virus (HIV) infection remains a significant challenge to global public health. Despite advances in antiretroviral therapy (ART), which has transformed HIV infection from a fatal disease into a manageable chronic condition, a definitive cure remains elusive. One of the key features of HIV infection is chronic immune activation and inflammation, which are strongly associated with, and predictive of, HIV disease progression, even in patients successfully treated with suppressive ART. Chronic inflammation is characterized by persistent inflammation, immune cell metabolic dysregulation, and cellular exhaustion and dysfunction. This review aims to summarize current knowledge of the interplay between chronic inflammation, immune metabolism, and T cell dysfunction in HIV infection, and also discusses the use of humanized mice models to study HIV immune pathogenesis and develop novel therapeutic strategies.

摘要

慢性人类免疫缺陷病毒(HIV)感染仍然是全球公共卫生的重大挑战。尽管抗逆转录病毒疗法(ART)取得了进展,将 HIV 感染从致命疾病转变为可控制的慢性疾病,但仍难以实现根治。HIV 感染的一个关键特征是慢性免疫激活和炎症,它与 HIV 疾病进展密切相关,并可预测疾病进展,即使在接受抑制性 ART 治疗的患者中也是如此。慢性炎症的特征是持续炎症、免疫细胞代谢失调以及细胞衰竭和功能障碍。本综述旨在总结目前对 HIV 感染中慢性炎症、免疫代谢和 T 细胞功能障碍之间相互作用的认识,并讨论使用人源化小鼠模型研究 HIV 免疫发病机制和开发新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d7d/10893210/91237aef98da/viruses-16-00219-g001.jpg

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