Duke Transplant Center, Department of Surgery, Duke University Medical Center, Durham, NC, United States.
Front Immunol. 2021 Jun 11;12:694763. doi: 10.3389/fimmu.2021.694763. eCollection 2021.
There is an urgent need for therapeutic interventions for desensitization and antibody-mediated rejection (AMR) in sensitized patients with preformed or donor-specific HLA antibodies (DSA). The risk of AMR and allograft loss in sensitized patients is increased due to preformed DSA detected at time of transplant or the reactivation of HLA memory after transplantation, causing acute and chronic AMR. Alternatively, DSA that develops post-transplant due to inadequate immunosuppression and again may lead to acute and chronic AMR or even allograft loss. Circulating antibody, the final product of the humoral immune response, has been the primary target of desensitization and AMR treatment. However, in many cases these protocols fail to achieve efficient removal of all DSA and long-term outcomes of patients with persistent DSA are far worse when compared to non-sensitized patients. We believe that targeting multiple components of humoral immunity will lead to improved outcomes for such patients. In this review, we will briefly discuss conventional desensitization methods targeting antibody or B cell removal and then present a mechanistically designed desensitization regimen targeting plasma cells and the humoral response.
对于致敏患者中预先存在或供体特异性 HLA 抗体(DSA)介导的抗体致敏和抗体介导的排斥反应(AMR),迫切需要治疗干预措施。由于在移植时检测到预先存在的 DSA 或移植后 HLA 记忆的重新激活,导致急性和慢性 AMR,因此致敏患者的 AMR 和移植物丢失的风险增加。或者,由于免疫抑制不足而在移植后发展的 DSA 也可能导致急性和慢性 AMR 甚至移植物丢失。循环抗体是体液免疫反应的最终产物,一直是脱敏和 AMR 治疗的主要靶点。然而,在许多情况下,这些方案未能有效去除所有 DSA,并且与非致敏患者相比,持续存在 DSA 的患者的长期结局要差得多。我们相信,针对体液免疫的多个成分将为这些患者带来更好的结果。在这篇综述中,我们将简要讨论针对抗体或 B 细胞清除的常规脱敏方法,然后提出一种针对浆细胞和体液反应的机制设计脱敏方案。