Tolerance has its limits: how the thymus copes with infection

被引:80
作者
Nunes-Alves, Claudio [1 ,2 ,3 ]
Nobrega, Claudia [1 ,2 ]
Behar, Samuel M. [3 ]
Correia-Neves, Margarida [1 ,2 ]
机构
[1] Univ Minho, Sch Hlth Sci, Life & Hlth Sci Res Inst ICVS, P-4710057 Braga, Portugal
[2] ICVS 3Bs, PT Govt Associate Lab, Braga, Portugal
[3] Univ Massachusetts, Sch Med, Dept Microbiol & Physiol Syst, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
thymus; infection; T cell repertoire; antimicrobial response; thymic microenvironment; TRYPANOSOMA-CRUZI INFECTION; MURINE LEUKEMIA-VIRUS; SCID-HU MOUSE; T-CELLS; IN-VIVO; EPITHELIAL-CELLS; HIV-1; INFECTION; IMMUNODEFICIENCY-VIRUS; PERSISTENT INFECTION; THYMOCYTE DEPLETION;
D O I
10.1016/j.it.2013.06.004
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 thymus is required for T cell differentiation; a process that depends on which antigens are encountered by thymocytes, the environment surrounding the differentiating cells, and the thymic architecture. These features are altered by local infection of the thymus and by the inflammatory mediators that accompany systemic infection. Although once believed to be an immune privileged site, it is now known that antimicrobial responses are recruited to the thymus. Resolving infection in the thymus is important because chronic persistence of microbes impairs the differentiation of pathogen-specific T cells and diminishes resistance to infection. Understanding how these mechanisms contribute to disease susceptibility, particularly in infants with developing T cell repertoires, requires further investigation.
引用
收藏
页码:502 / 510
页数:9
相关论文
共 75 条
[31]   T-CELL TOLERANCE - EXPOSURE TO VIRUS INUTERO DOES NOT CAUSE A PERMANENT DELETION OF SPECIFIC T-CELLS [J].
JAMIESON, BD ;
AHMED, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (07) :2265-2268
[32]   NEONATAL EXPOSURE TO THYMOTROPIC GROSS MURINE LEUKEMIA-VIRUS INDUCES VIRUS-SPECIFIC IMMUNOLOGICAL NONRESPONSIVENESS [J].
KOROSTOFF, JM ;
NAKADA, MT ;
FAAS, SJ ;
BLANK, KJ ;
GAULTON, GN .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (06) :1765-1775
[33]  
LAMONTAGNE L, 1994, LAB ANIM SCI, V44, P17
[34]   Antigen-specific and nonspecific deletion of immature cortical thymocytes caused by antigen injection [J].
Martin, S ;
Bevan, MJ .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (10) :2726-2736
[35]   Experimental Trypanosoma cruzi infection alters the shaping of the central and peripheral T-cell repertoire [J].
Mendes-da-Cruz, DA ;
de Meis, J ;
Cotta-de-Almeida, V ;
Savino, W .
MICROBES AND INFECTION, 2003, 5 (10) :825-832
[36]   Altered thymocyte migration during experimental acute Trypanosoma cruzi infection:: combined role of fibronectin and the chemokines CXCL12 and CCL4 [J].
Mendes-da-Cruz, Daniella Areas ;
Silva, Joao Santana ;
Cotta-de-Almeida, Vinicius ;
Savino, Wilson .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2006, 36 (06) :1486-1493
[37]   IS A FUNCTION OF THE SECRETED HEPATITIS-BE ANTIGEN TO INDUCE IMMUNOLOGICAL-TOLERANCE INUTERO [J].
MILICH, DR ;
JONES, JE ;
HUGHES, JL ;
PRICE, J ;
RANEY, AK ;
MCLACHLAN, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6599-6603
[38]   Role of thymic output in regulating CD8 T-cell homeostasis during acute and chronic viral infection [J].
Miller, NE ;
Bonczyk, JR ;
Nakayama, Y ;
Suresh, M .
JOURNAL OF VIROLOGY, 2005, 79 (15) :9419-9429
[39]   HUMAN CYTOMEGALOVIRUS IN A SCID-HU MOUSE - THYMIC EPITHELIAL-CELLS ARE PROMINENT TARGETS OF VIRAL REPLICATION [J].
MOCARSKI, ES ;
BONYHADI, M ;
SALIMI, S ;
MCCUNE, JM ;
KANESHIMA, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :104-108
[40]   Peripheral CD4+CD8+ T cells are differentiated effector memory cells with antiviral functions [J].
Nascimbeni, M ;
Shin, EC ;
Chiriboga, L ;
Kleiner, DE ;
Rehermann, B .
BLOOD, 2004, 104 (02) :478-486