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

Author:

Mu Wenli12ORCID,Patankar Vaibhavi12,Kitchen Scott12,Zhen Anjie12

Affiliation:

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

2. 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

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.

Funder

National Institute of Allergy and Infectious Diseases

National Institute on Drug Abuse

Foundation for AIDS Research

National Cancer Institute

NIH

California Institute for Regenerative Medicine

California HIV/AIDS Research Program

UCLA AIDS Institute

James B. Pendleton Charitable Trust

McCarthy Family Foundation

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

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