4.7 Review

Allorecognition and the spectrum of kidney transplant rejection

期刊

KIDNEY INTERNATIONAL
卷 101, 期 4, 页码 692-710

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.kint.2021.11.029

关键词

antibody-dependent cellular cytotoxicity; autoantibodies; complement-dependent cytotoxicity; delayed type hypersensitivity; graft failure; missing self; monocytes; natural killer cells; reclassification

资金

  1. Research Foundation Flanders (F.W.O.) [1844019N, 1196119N]

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The detection of mismatched human leukocyte antigens by adaptive immune cells is the main cause of transplant rejection. However, recent observations have questioned the traditional dichotomy between T-cell mediated rejection and antibody-mediated rejection, leading to a need for a more integrated view of kidney transplant rejection. This review highlights the gaps in the current classification of rejection, provides an overview of the expanding insights into the mechanisms of allorecognition, and discusses how these insights could improve our understanding and clinical approach to kidney transplant rejection.
Detection of mismatched human leukocyte antigens by adaptive immune cells is considered as the main cause of transplant rejection, leading to either T-cell mediated rejection or antibody-mediated rejection. This canonical view guided the successful development of immunosuppressive therapies and shaped the diagnostic Banff classification for kidney transplant rejection that is used in clinics worldwide. However, several observations have recently emerged that question this dichotomization between T-cell mediated rejection and antibody-mediated rejection, related to heterogeneity in the serology, histology, and prognosis of the rejection phenotypes. In parallel, novel insights were obtained concerning the dynamics of donor-specific anti-human leukocyte antigen antibodies, the immunogenicity of donor-recipient non-human leukocyte antigen mismatches, and the autoreactivity against self-antigens. Moreover, the potential of innate allorecognition was uncovered, as exemplified by natural killer cell-mediated microvascular inflammation through missing self, and by the emerging evidence on monocyte-driven allorecognition. In this review, we highlight the gaps in the current classification of rejection, provide an overview of the expanding insights into the mechanisms of allorecognition, and critically appraise how these could improve our understanding and clinical approach to kidney transplant rejection. We argue that consideration of the complex interplay of various allorecognition mechanisms can foster a more integrated view of kidney transplant rejection and can lead to improved risk stratification, targeted therapies, and better outcome after kidney transplantation.

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