Graft rejection mediated by CD4+ T cells via indirect recognition of alloantigen is associated with a dominant Th2 response

被引:21
作者
Csencsits, K
Wood, SC
Lu, GY
Magee, JC
Eichwald, EJ
Chang, CH
Bishop, DK
机构
[1] Univ Michigan, Med Ctr, Sch Med, Sect Gen Surg,Dept Surg, Ann Arbor, MI 48109 USA
[2] Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT USA
[3] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
[4] Univ Michigan, Sch Med, Dept Microbiol & Immunol, Ann Arbor, MI 48109 USA
关键词
transplantation; antigen recognition; T cells; Th1/Th2;
D O I
10.1002/eji.200425685
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) T cells that respond to indirectly presented alloantigen have been shown to mediate chronic rejection, however, the role of the indirect pathway in acute rejection has yet to be completely elucidated. To this end, BALB/c or C57BL/6 mice were depleted of CD8(+) T cells and transplanted with class II transactivator (CIITA)-deficient cardiac allografts, which cannot directly present class II alloantigens to CD4(+) T cells. In this manner, the rejection response by CD4(+) cells was forced to rely upon the indirect recognition pathway. When not depleted of CD8(+) cells, both BALB/c and C57BL/6 mice rejected CIITA-/- allografts and a polarized Th1 response was observed. In contrast, when BALB/c recipients of CIITA-/- allografts were depleted of CD8(+) T cells, the grafts were acutely rejected and a strong Th2 response characterized by eosinophil influx into the graft was observed. Interestingly, CD8-depleted C57BL/6 recipients of CIITA-/-allografts did not acutely reject their transplants and a Th2 response was not mounted. These findings indicate that CD4(+) T cells responding to indirectly presented alloantigens mediate graft rejection in a Th2-dominant manner, and provide further evidence for the role of Th2 responses in acute graft rejection.
引用
收藏
页码:843 / 851
页数:9
相关论文
共 59 条
[21]   Indirect allorecognition can play an important role in the development of transplant arteriosclerosis [J].
Ensminger, SM ;
Spriewald, BM ;
Witzke, O ;
Pajaro, OE ;
Yacoub, MH ;
Morris, PJ ;
Rose, ML ;
Wood, KJ .
TRANSPLANTATION, 2002, 73 (02) :279-286
[22]   H2-DMα-/- mice show the importance of major histocompatibility complex-bound peptide in cardiac allograft rejection [J].
Felix, NJ ;
Brickey, WJ ;
Griffiths, R ;
Zhang, JH ;
Van Kaer, L ;
Coffman, T ;
Ting, JPY .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (01) :31-40
[23]   Comparison of Abβb-/-, H2-DM-, and CIITA-/- in second-set skin allograft rejection [J].
Felix, NJ ;
de Serres, S ;
Meyer, AA ;
Ting, JPY .
JOURNAL OF SURGICAL RESEARCH, 2002, 102 (02) :185-192
[24]   IL-4 and T cells are required for the generation of IgG1 isotype antibodies against cardiolipin [J].
Fischer, K ;
Collins, H ;
Taniguchi, M ;
Kaufmann, SHE ;
Schaible, UE .
JOURNAL OF IMMUNOLOGY, 2002, 168 (06) :2689-2694
[25]   Dendritic cells prime in vivo alloreactive CD4 T lymphocytes toward type 2 cytokine- and TGF-β-producing cells in the absence of CD8 T cell activation [J].
Foucras, G ;
Coudert, JD ;
Coureau, C ;
Guéry, JC .
JOURNAL OF IMMUNOLOGY, 2000, 165 (09) :4994-5003
[26]   Structures of an MHC class II molecule with covalently bound single peptides [J].
Fremont, DH ;
Hendrickson, WA ;
Marrack, P ;
Kappler, J .
SCIENCE, 1996, 272 (5264) :1001-1004
[27]   A role for eosinophils in transplant rejection [J].
Goldman, M ;
Le Moine, A ;
Braun, M ;
Flamand, V ;
Abramowicz, D .
TRENDS IN IMMUNOLOGY, 2001, 22 (05) :247-251
[28]   Direct and indirect recognition: the role of MHC antigens in graft rejection [J].
Gould, DS ;
Auchincloss, H .
IMMUNOLOGY TODAY, 1999, 20 (02) :77-82
[29]  
Hondowicz BD, 2000, EUR J IMMUNOL, V30, P2007, DOI 10.1002/1521-4141(200007)30:7&lt
[30]  
2007::AID-IMMU2007&gt