Current Therapies in Kidney Transplant Rejection

被引:9
|
作者
Alasfar, Sami [1 ]
Kodali, Lavanya [1 ]
Schinstock, Carrie A. [2 ]
机构
[1] Mayo Clin, Dept Med, Phoenix, AZ 85054 USA
[2] Mayo Clin, Dept Med, Rochester, MN 55905 USA
关键词
rejection; transplantation; kidney transplant; ANTIBODY-MEDIATED REJECTION; RENAL-ALLOGRAFT REJECTION; PLASMA-EXCHANGE; INTRAVENOUS IMMUNOGLOBULIN; PROTEASOME INHIBITION; HUMORAL REJECTION; CROSS-MATCH; PLASMAPHERESIS; ECULIZUMAB; RECIPIENTS;
D O I
10.3390/jcm12154927
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Despite significant advancements in immunosuppressive therapies, kidney transplant rejection continues to pose a substantial challenge, impacting the long-term survival of grafts. This article provides an overview of the diagnosis, current therapies, and management strategies for acute T-cell-mediated rejection (TCMR) and antibody-mediated rejection (ABMR). TCMR is diagnosed through histological examination of kidney biopsy samples, which reveal the infiltration of mononuclear cells into the allograft tissue. Corticosteroids serve as the primary treatment for TCMR, while severe or steroid-resistant cases may require T-cell-depleting agents, like Thymoglobulin. ABMR occurs due to the binding of antibodies to graft endothelial cells. The most common treatment for ABMR is plasmapheresis, although its efficacy is still a subject of debate. Other current therapies, such as intravenous immunoglobulins, anti-CD20 antibodies, complement inhibitors, and proteasome inhibitors, are also utilized to varying degrees, but their efficacy remains questionable. Management decisions for ABMR depend on the timing of the rejection episode and the presence of chronic changes. In managing both TCMR and ABMR, it is crucial to optimize immunosuppression and address adherence. However, further research is needed to explore newer therapeutics and evaluate their efficacy.
引用
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页数:13
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