Accommodation in allogeneic and xenogeneic organ transplantation: Prevalence, impact, and implications for monitoring and for therapeutics

被引:5
|
作者
Platt, Jeffrey L.
Cascalho, Marilia
机构
[1] Univ Michigan, Dept Surg, Ann Arbor, MI USA
[2] Univ Michigan, Dept Microbiol & Immunol, Ann Arbor, MI USA
基金
美国国家卫生研究院;
关键词
ABO-incompatible transplant; Accommodation; Allograft; Antibody; Antibody-mediated rejection; B cell; Complement; Complement activation; Endothelial cell activation; Heparan sulfate; Organ transplant; Rejection; Xenograft; ACUTE-VASCULAR-REJECTION; PORCINE ENDOTHELIAL-CELLS; DONOR-SPECIFIC ANTIBODY; MEMBRANE-ATTACK COMPLEX; INCOMPATIBLE KIDNEY-TRANSPLANTATION; HEPARAN-SULFATE PROTEOGLYCAN; DECAY-ACCELERATING FACTOR; HYPERACUTE REJECTION; RENAL-TRANSPLANTATION; MEDIATED REJECTION;
D O I
10.1016/j.humimm.2022.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Accommodation refers to acquired resistance of organs or tissues to immune or inflammatory reactions that might otherwise cause severe injury or rejection. As first observed in ABO-incompatible kidney transplants and heterotopic cardiac xenografts, accommodation was identified when organ transplants continued to func-tion despite the presence of anti-graft antibodies and/or other reactants in the blood of recipients. Recent evi-dence suggests many and perhaps most organ transplants have accommodation, as most recipients mount B cell responses specific for the graft. Wide interest in the impact of graft-specific antibodies on the outcomes of trans-plants prompts questions about which mechanisms confer protection against such antibodies, how accommo-dation might be detected and whether and how rejection could be superimposed on accommodation. Xenotransplantation offers a unique opportunity to address these questions because immune responses to xeno-grafts are easily detected and the pathogenic impact of immune responses is so severe. Xenotransplantation also provides a compelling need to apply these and other insights to decrease the intensity and toxicity of immunosuppression that otherwise could limit clinical application.
引用
收藏
页码:5 / 17
页数:13
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