Functional Compartmentalization of Antibodies in the Central Nervous System During Chronic HIV Infection

被引:6
作者
Spatola, Marianna [1 ]
Loos, Carolin [1 ,2 ]
Cizmeci, Deniz [1 ,2 ]
Webb, Nicholas [1 ]
Gorman, Matthew J. [1 ]
Rossignol, Evan [1 ]
Shin, Sally [1 ]
Yuan, Dansu [1 ]
Fontana, Laura [1 ]
Mukerji, Shibani S. [3 ]
Lauffenburger, Douglas A. [2 ]
Gabuzda, Dana [4 ]
Alter, Galit [1 ]
机构
[1] MIT, Ragon Inst MGH, 400 Technol Sq, Cambridge, MA 02139 USA
[2] MIT, Cambridge, MA 02139 USA
[3] Massachusetts Gen Hosp, Boston, MA 02114 USA
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
基金
美国国家卫生研究院; 瑞士国家科学基金会;
关键词
cerebrospinal fluid; plasma; antibody functions; complement deposition; phagocytosis; NK activation; Fc receptors; ART; HIV-associated neurocognitive disorders; FC-RECEPTOR FCRN; ANTIRETROVIRAL THERAPY; CEREBROSPINAL-FLUID; NEUROCOGNITIVE IMPAIRMENT; HIGH-THROUGHPUT; IGG TRANSPORT; COMPLEMENT; BRAIN; RNA; INFLAMMATION;
D O I
10.1093/infdis/jiac138
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The central nervous system (CNS) has emerged as a critical HIV reservoir. Thus, interventions aimed at controlling and eliminating HIV must include CNS-targeted strategies. Given the inaccessibility of the brain, efforts have focused on cerebrospinal fluid (CSF), aimed at defining biomarkers of HIV-disease in the CNS, including HIV-specific antibodies. However, how antibodies traffic between the blood and CNS, and whether specific antibody profiles track with HIV-associated neurocognitive disorders (HAND) remains unclear. Here, we comprehensively profiled HIV-specific antibodies across plasma and CSF from 20 antiretroviral therapy (ART) naive or treated persons with HIV. CSF was populated by IgG1 and IgG3 antibodies, with reduced Fc-effector profiles. While ART improved plasma antibody functional coordination, CSF profiles were unaffected by ART and were unrelated to HAND severity. These data point to a functional sieving of antibodies across the blood-brain barrier, providing previously unappreciated insights for the development of next-generation therapeutics targeting the CNS reservoir.
引用
收藏
页码:738 / 750
页数:13
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