Suppression of T and B lymphocyte activation by a Yersinia pseudotuberculosis virulence factor, YopH

被引:112
作者
Yao, T
Mecsas, J
Healy, JI
Falkow, S
Chien, YH
机构
[1] Stanford Univ, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[2] Stanford Univ, Program Immunol, Stanford, CA 94305 USA
关键词
T cell; B cell; Yersinia pseudotuberculosis; bacterial pathogenesis YopH;
D O I
10.1084/jem.190.9.1343
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 acquired immune responses are crucial to the: survival of Yersinia-infected animals. Mice lacking T cells are sensitive to Yersinia infection, and a humoral response to Yersinia can be protective. Diverse mechanisms for Yersinia to impair and evade the host innate immune defense have been suggested, but the effects of Yersinia on lymphocytes are not known. Here, we demonstrate that after a transient exposure to Y. pseudotuberculosis, T and B cells are impaired in their ability to be activated through their antigen receptors. T cells are inhibited in their ability to produce cytokines, and B cells are unable to upregulate surface expression of the costimulatory molecule, B7.2, in response to antigenic stimulation. The block of lymphocyte activation results fi-om the inhibition of early phosphorylation events of the antigen receptor signaling complex. Through the use of Y. pseudotuberculosis mutants, wr show that the inhibitory effect in both T cells and B cells is dependent on the production of Yersinia outermembrane protein (Yop) H, a tyrosine phosphatase. Our results suggest a mechanism by which the pathogenic bacteria may modulate a wide range of T and B cell-mediated immune responses.
引用
收藏
页码:1343 / 1350
页数:8
相关论文
共 55 条
[21]   Different nuclear signals are activated by the B cell receptor during positive versus negative signaling [J].
Healy, JI ;
Dolmetsch, RE ;
Timmerman, LA ;
Cyster, JG ;
Thomas, ML ;
Crabtree, GR ;
Lewis, RS ;
Goodnow, CC .
IMMUNITY, 1997, 6 (04) :419-428
[22]  
HOLMSTROM A, 1995, INFECT IMMUN, V63, P2269
[23]   YopT, a new Yersinia Yop effector protein, affects the cytoskeleton of host cells [J].
Iriarte, M ;
Cornelis, GR .
MOLECULAR MICROBIOLOGY, 1998, 29 (03) :915-929
[24]   IDENTIFICATION OF INVASIN - A PROTEIN THAT ALLOWS ENTERIC BACTERIA TO PENETRATE CULTURED-MAMMALIAN-CELLS [J].
ISBERG, RR ;
VOORHIS, DL ;
FALKOW, S .
CELL, 1987, 50 (05) :769-778
[25]   MULTIPLE BETA-1-CHAIN INTEGRINS ARE RECEPTORS FOR INVASIN, A PROTEIN THAT PROMOTES BACTERIAL PENETRATION INTO MAMMALIAN-CELLS [J].
ISBERG, RR ;
LEONG, JM .
CELL, 1990, 60 (05) :861-871
[26]   Ligation of the T cell antigen receptor induces tyrosine phosphorylation of p105(CasL), a member of the p130(Cas-)-related docking protein family, and its subsequent binding to the Src homology 2 domain of c-Crk [J].
Kanda, H ;
Mimura, T ;
Morino, N ;
Hamasaki, K ;
Nakamoto, T ;
Hirai, H ;
Morimoto, C ;
Yazaki, Y ;
Nojima, Y .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1997, 27 (08) :2113-2117
[27]   A secreted protein tyrosine phosphatase with modular effector domains in the bacterial pathogen Salmonella typhimurium [J].
Kaniga, K ;
Uralil, J ;
Bliska, JB ;
Galan, JE .
MOLECULAR MICROBIOLOGY, 1996, 21 (03) :633-641
[28]   THE YOPM GENE OF YERSINIA-PESTIS ENCODES A RELEASED PROTEIN HAVING HOMOLOGY WITH THE HUMAN-PLATELET SURFACE PROTEIN GPIB-ALPHA [J].
LEUNG, KY ;
STRALEY, SC .
JOURNAL OF BACTERIOLOGY, 1989, 171 (09) :4623-4632
[29]   YOPM INHIBITS PLATELET-AGGREGATION AND IS NECESSARY FOR VIRULENCE OF YERSINIA-PESTIS IN MICE [J].
LEUNG, KY ;
REISNER, BS ;
STRALEY, SC .
INFECTION AND IMMUNITY, 1990, 58 (10) :3262-3271
[30]   Invasin of Yersinia pseudotuberculosis activates human peripheral B cells [J].
Lundgren, E ;
Carballeira, N ;
Vazquez, R ;
Dubinina, E ;
Branden, H ;
Persson, H ;
WolfWatz, H .
INFECTION AND IMMUNITY, 1996, 64 (03) :829-835