Immune responses in 4-1BB (CD137)-deficient mice

被引:179
作者
Kwon, BS [1 ]
Hurtado, JC
Lee, ZH
Kwack, KB
Seo, SK
Choi, BK
Koller, BH
Wolisi, G
Broxmeyer, HE
Vinay, DS
机构
[1] Univ Ulsan, Immunomodulat Res Ctr, Ulsan, South Korea
[2] Louisiana State Univ, Ctr Eye, Hlth Sci Ctr, Sch Med, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Dept Ophthalmol, Hlth Sci Ctr, Sch Med, New Orleans, LA 70112 USA
[4] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Med, Walther Canc Inst, Indianapolis, IN 46202 USA
[6] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[7] Chosun Univ, Sch Dent, Dept Microbiol & Immunol, Kwangzu, South Korea
[8] Univ N California, Dept Med, Chapel Hill, NC 27559 USA
[9] Univ Michigan, Sch Med, Dept Gen Surg, Ann Arbor, MI 48109 USA
关键词
D O I
10.4049/jimmunol.168.11.5483
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 4-1BB (a TNFR superfamily member) is an inducible costimulatory molecule that can exert regulatory effects on T cells independently of CD28 stimulation. The in vitro expression of 4-1BB (CD137) is induced following activation of T cells with various stimuli, including anti-TCR mAbs, lectins, and a combination of PMA and ionomycin. To delineate further the physiological role of 4-1BB in immunity, mice deficient in this receptor were generated. These mutant mice developed normally, and were viable and fertile. Humoral responses to vesicular stomatitis virus were comparable with those seen in wild-type mice, whereas the IgG2a and IgG3 isotype responses to keyhole limpet hemocyanin were somewhat reduced in the mutant mice. The 4-1BB-deficient mice demonstrated enhanced T cell proliferation in response to mitogens or anti-CD3 even in the environment of reduced ability to secrete growth-supporting cytokines (IL-2 and IL-4). Although T cells from 4-1BB-deficient mice showed enhanced proliferation, the T cell immune responses of these animals, such as cytokine production and CTL activity, were diminished. In addition, 4-1BB deletion appears to play a role in the regulation of myeloid progenitor cell growth, leading to an increase in these precursor cells in peripheral blood, bone marrow, and spleen.
引用
收藏
页码:5483 / 5490
页数:8
相关论文
共 30 条
[1]   4-1BB and Ox40 are members of a tumor necrosis factor (TNF)-nerve growth factor receptor subfamily that bind TNF receptor-associated factors and activate nuclear factor κB [J].
Arch, RH ;
Thompson, CB .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (01) :558-565
[2]  
BACHMANN MF, 1995, J IMMUNOL, V155, P3727
[3]   Ligation of 4-1BB (CDw137) regulates graft-versus-host disease, graft-versus-leukemia, and graft rejection in allogeneic bone marrow transplant recipients [J].
Blazar, BR ;
Kwon, BS ;
Panoskaltsis-Mortari, A ;
Kwak, KB ;
Peschon, JJ ;
Taylor, PA .
JOURNAL OF IMMUNOLOGY, 2001, 166 (05) :3174-3183
[4]  
BROXMEYER HE, 1995, ANN HEMATOL, V71, P235, DOI 10.1007/s002770050112
[5]  
Broxmeyer HE, 1999, CYTOKINES IN THE TREATMENT OF HEMATOPOIETIC FAILURE, P1
[6]  
BRUNNER KT, 1968, IMMUNOLOGY, V14, P181
[7]  
Cooper S, 1996, CURRENT PROTOCOLS IM
[8]   ROLE OF 4-1BB-LIGAND IN COSTIMULATION OF T-LYMPHOCYTE GROWTH AND ITS UP-REGULATION ON M12 B-LYMPHOMAS BY CAMP [J].
DEBENEDETTE, MA ;
CHU, NR ;
POLLOK, KE ;
HURTADO, J ;
WADE, WF ;
KWON, BS ;
WATTS, TH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (03) :985-992
[9]  
DeBenedette MA, 1999, J IMMUNOL, V163, P4833
[10]  
FINKELMAN FD, 1988, J IMMUNOL, V140, P1022