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Transfusion of minor histocompatibility antigen–mismatched platelets induces rejection of bone marrow transplants in mice

机译:输血的组织相容性较弱的血小板失配可诱导小鼠骨髓移植排斥

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摘要

Bone marrow transplantation (BMT) represents a cure for nonmalignant hematological disorders. However, compared with the stringent conditioning regimens used when performing BMT to treat hematological malignancies, the reduced intensity conditioning regimen used in the context of nonmalignant hematological disorders leads to substantially higher rates of BMT rejection, presumably due to an intact immune system. The relevant patient population typically receives transfusion support, often including platelets, and the frequency of BMT rejection correlates with the frequency of transfusion. Here, we demonstrate that immunity to transfused platelets contributes to subsequent BMT rejection in mice, even when the BMT donor and recipient are MHC matched. We used MHC-matched bone marrow because, although immunity to transfused platelets is best characterized in relation to HLA-specific antibodies, such antibodies are unlikely to play a role in clinical BMT rejection that is HLA matched. However, bone marrow is not matched in the clinic for minor histocompatibility antigens, such as those carried by platelets, and we report that transfusion of minor histocompatibility antigen–mismatched platelets induced subsequent BMT rejection. These findings indicate previously unappreciated sequelae of immunity to platelets in the context of transplantation and suggest that strategies to account for minor histocompatibility mismatching may help to reduce the chance of BMT rejection in human patients.
机译:骨髓移植(BMT)代表了非恶性血液病的治疗方法。但是,与进行BMT来治疗血液恶性肿瘤时使用的严格条件相比,在非恶性血液系统疾病中使用降低强度的条件可以导致BMT排斥率大大提高,这可能是由于免疫系统完整所致。相关的患者人群通常会接受输血支持,通常包括血小板,BMT排斥的频率与输血频率相关。在这里,我们证明了即使在BMT供体和受体都与MHC匹配的情况下,对输注血小板的免疫也会导致随后的BMT排斥。我们使用了MHC匹配的骨髓,因为,尽管相对于HLA特异性抗体,对输注血小板的免疫性得到了最好的表征,但此类抗体不太可能在与HLA匹配的临床BMT排斥中发挥作用。但是,在临床上,骨髓中的组织相容性较弱的抗原(如血小板携带的抗原)并不匹配,因此我们报道输血的组织相容性较弱的血小板与血小板不匹配会导致随后的BMT排斥。这些发现表明,在移植的背景下,先前对血小板免疫的后遗症并未得到重视,并且表明解决轻微组织相容性不匹配的策略可能有助于减少人类患者发生BMT排斥的机会。

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