Unlinked Memory Helper Responses Promote Long-Lasting Humoral Alloimmunity

被引:18
作者
Conlon, Thomas M. [1 ]
Cole, Jennifer L. [1 ]
Motallebzadeh, Reza [1 ]
Harper, Ines [1 ]
Callaghan, Chris J. [1 ]
Bolton, Eleanor M. [1 ]
Bradley, J. Andrew [1 ]
Saeb-Parsy, Kourosh [1 ]
Pettigrew, Gavin J. [1 ]
机构
[1] Univ Cambridge, Dept Surg, Cambridge CB2 0QQ, England
基金
英国惠康基金;
关键词
CD4; T-CELLS; FOLLICULAR DENDRITIC CELLS; B-CELLS; ALLOGRAFT-REJECTION; ALLOANTIBODY PRODUCTION; HEART-TRANSPLANTATION; ANTIBODY-RESPONSES; INDIRECT-PATHWAY; GRAFT-REJECTION; ACQUIRE ANTIGEN;
D O I
10.4049/jimmunol.1202257
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Essential help for long-lived alloantibody responses is theoretically provided only by CD4 T cells that recognize target alloantigen, processed and presented by the allospecific B cell. We demonstrate that in an alloresponse to multiple MHC disparities, cognate help for class-switched alloantibody may also be provided by CD4 T cells specific for a second "helper" alloantigen. This response was much shorter-lived than when help was provided conventionally, by Th cell recognition of target alloantigen. Nevertheless, long-lasting humoral alloimmunity developed when T cell memory against the helper alloantigen was first generated. Costimulatory blockade abrogated alloantibody produced through naive Th cell recognition of target alloantigen but, crucially, blockade was ineffective when help was provided by memory responses to the accessory helper alloantigen. These results suggest that memory Th cell responses against previously encountered graft alloantigen may be the dominant mechanism for providing help to generate new specificities of alloantibody in transplant patients receiving immunosuppression. The Journal of Immunology, 2012, 189: 5703-5712.
引用
收藏
页码:5703 / 5712
页数:10
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