Pulmonary Innate Immune Dysfunction in Human Immunodeficiency Virus

被引:7
|
作者
Staitieh, Bashar S. [1 ]
Egea, Eduardo E. [1 ]
Guidot, David M. [1 ,2 ]
机构
[1] Emory Univ, Sch Med, Div Pulm Allergy Crit Care & Sleep Med, 615 Michael St,Suite 205, Atlanta, GA 30322 USA
[2] Atlanta Vet Adm Med Ctr, Decatur, GA USA
基金
美国国家卫生研究院;
关键词
innate immunity; human immunodeficiency virus; macrophage; surfactant; polymorphonuclear cells; ALVEOLAR MACROPHAGES; HIV-1; INFECTION; NEUTROPHIL FUNCTION; DC-SIGN; SURFACTANT; PROTEIN; EXPRESSION; CELLS; PHAGOCYTOSIS; TUBERCULOSIS;
D O I
10.1165/rcmb.2016-0213TR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The advent of antiretroviral therapy has transformed infection by the type 1humanimmunodeficiency virus (HIV) froma rapidly fatal disease to a chronic illness with excellent long-term survival rates. Although HIV primarily targets the adaptive arm of host immunity, it simultaneously impacts the innate immune system, and has profound implications for lung health, even when viral suppression is achieved with antiretroviral therapy. The lung has evolved a unique array of innate immune defenses, and the pathophysiological interactions between HIV and the pulmonary innate immune system deserve particular attention. In this review, we discuss work that elucidates how the components of innate immunity both respond to and are perturbed by infection with HIV.
引用
收藏
页码:563 / 567
页数:5
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