The Lymph Node in HIV Pathogenesis

被引:31
作者
Dimopoulos, Yiannis [1 ]
Moysi, Eirini [1 ]
Petrovas, Constantinos [1 ]
机构
[1] NIAID, Tissue Anal Core, Vaccine Res Ctr, NIH, 40 Convent Dr,MSC 3022,Bldg 40,Room 3612B, Bethesda, MD 20892 USA
关键词
Lymph nodes; Pathogenesis; HIV; HIV/SIV pathogenesis; HIV-infected lymph nodes; T FOLLICULAR HELPER; INFECTED RHESUS MACAQUES; DENDRITIC CELL NETWORKS; LYMPHOTOXIN BETA; TISSUE STRUCTURE; IMMUNE-RESPONSE; REPLICATION; DYNAMICS; RECONSTITUTION; MACROPHAGES;
D O I
10.1007/s11904-017-0359-7
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Lymph nodes play a central role in the development of adaptive immunity against pathogens and particularly the generation of antigen-specific B cell responses in specialized areas called germinal centers (GCs). Lymph node (LN) pathology was recognized as an important consequence of human immunodeficiency virus (HIV) infection since the beginning of the HIV epidemic. Investigation into the structural and functional alterations induced by HIV and Simian immunodeficiency virus (SIV) has further cemented the central role that lymphoid tissue plays in HIV/SIV pathogenesis. The coexistence of constant local inflammation, altered tissue architecture, and relative exclusion of virus-specific CD8 T cells from the GCs creates a unique environment for the virus evolution and establishment of viral reservoir in specific GC cells, namely T follicular helper CD4 T cells (Tfh). A better understanding of the biology of immune cells in HIV-infected lymph nodes is a prerequisite to attaining the ultimate goal of complete viral eradication.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 93 条
[1]   Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice [J].
Alimzhanov, MB ;
Kuprash, DV ;
KoscoVilbois, MH ;
Luz, A ;
Turetskaya, RL ;
Tarakhovsky, A ;
Rajewsky, K ;
Nedospasov, SA ;
Pfeffer, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (17) :9302-9307
[2]   Follicular dendritic cell networks of primary follicles and germinal centers: Phenotype and function [J].
Allen, Christopher D. C. ;
Cyster, Jason G. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (01) :14-25
[3]   Germinal-center organization and cellular dynamics [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Cyster, Jason G. .
IMMUNITY, 2007, 27 (02) :190-202
[4]  
[Anonymous], 2016, Global AIDS Update 2016
[5]   Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes [J].
Bajenoff, Marc ;
Egen, Jackson G. ;
Koo, Lily Y. ;
Laugier, Jean Pierre ;
Brau, Frederic ;
Glaichenhaus, Nicolas ;
Germain, Ronald N. .
IMMUNITY, 2006, 25 (06) :989-1001
[6]  
Baroni C D, 1990, Prog AIDS Pathol, V2, P33
[7]   Persistent Antigen and Germinal Center B Cells Sustain T Follicular Helper Cell Responses and Phenotype [J].
Baumjohann, Dirk ;
Preite, Silvia ;
Reboldi, Andrea ;
Ronchi, Francesca ;
Ansel, K. Mark ;
Lanzavecchia, Antonio ;
Sallusto, Federica .
IMMUNITY, 2013, 38 (03) :596-605
[8]   Macrophage Infection via Selective Capture of HIV-1-Infected CD4+ T Cells [J].
Baxter, Amy E. ;
Russell, Rebecca A. ;
Duncan, Christopher J. A. ;
Moore, Michael D. ;
Willberg, Christian B. ;
Pablos, Jose L. ;
Finzi, Andres ;
Kaufmann, Daniel E. ;
Ochsenbauer, Christina ;
Kappes, John C. ;
Groot, Fedde ;
Sattentau, Quentin J. .
CELL HOST & MICROBE, 2014, 16 (06) :711-721
[9]   Follicular B helper T cells express CXC chemokine receptor 5, localize to B cell follicles, and support immunoglobulin production [J].
Breitfeld, D ;
Ohl, L ;
Kremmer, E ;
Ellwart, J ;
Sallusto, F ;
Lipp, M ;
Förster, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (11) :1545-1551
[10]   Differential infection patterns of CD4+ T cells and lymphoid tissue viral burden distinguish progressive and nonprogressive lentiviral infections [J].
Brenchley, Jason M. ;
Vinton, Carol ;
Tabb, Brian ;
Hao, Xing Pei ;
Connick, Elizabeth ;
Paiardini, Mirko ;
Lifson, Jeffrey D. ;
Silvestri, Guido ;
Estes, Jacob D. .
BLOOD, 2012, 120 (20) :4172-4181