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Unlinked memory helper responses promote long-lasting humoral alloimmunity

机译:未连接的记忆辅助反应促进持久的体液alloimmunity

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摘要

Essential help for long-lived alloantibody responses is theoretically provided only by CD4 T cells that recognise 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 helper T cell recognition of target alloantigen. Nevertheless, long-lasting humoral alloimmunity developed when T cell memory against the helper alloantigen was first generated. Co-stimulatory blockade abrogated alloantibody produced through naive helper T 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 helper T 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.
机译:理论上,只有通过识别目标同种抗原,由同种异体B细胞处理并呈递的CD4 T细胞才能提供长寿同种抗体反应的基本帮助。我们证明,在对多个MHC差异的过敏反应中,对于第二个“辅助”同种异体抗原特异的CD4 T细胞也可能为类转换同种异体抗体提供同类帮助。这种反应的寿命比传统上通过辅助T细胞识别靶同种异体抗原提供帮助时要短得多。然而,当首次产生针对辅助同种异体抗原的T细胞记忆时,便形成了持久的体液同种免疫。共刺激性阻断消除了由于天真辅助T细胞识别靶同种异体抗原而产生的同种异体抗体,但至关重要的是,当对辅助性辅助同种异体抗原的记忆反应提供帮助时,阻断无效。这些结果表明,针对先前遇到的移植同种异体抗原的记忆辅助T细胞反应可能是主要的机制,可为接受免疫抑制的移植患者提供帮助,以产生同种抗体的新特异性。

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