From Humoral Theory to Performant Risk Stratification in Kidney Transplantation

被引:31
作者
Lefaucheur, C. [1 ,2 ]
Viglietti, D. [1 ,2 ]
Mangiola, M. [3 ]
Loupy, A. [1 ,4 ]
Zeevi, A. [3 ]
机构
[1] INSERM, Paris Translat Res Ctr Organ Transplantat, UMR S970, Paris, France
[2] St Louis Hosp, AP HP, Kidney Transplant Dept, Paris, France
[3] Univ Pittsburgh, Med Ctr, Dept Transplant Pathol, Pittsburgh, PA USA
[4] Hop Necker Enfants Malad, AP HP, Kidney Transplant Dept, Paris, France
关键词
ANTIBODY-MEDIATED REJECTION; DONOR-SPECIFIC ANTIBODIES; HLA ANTIBODIES; CROSS-MATCH; COMPLEMENT-BINDING; IMMUNOGLOBULIN-G; GRAFT FAILURE; LIVER-TRANSPLANTATION; ALLOGRAFT SURVIVAL; RECIPIENTS;
D O I
10.1155/2017/5201098
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The purpose of the present review is to describe how we improve the model for risk stratification of transplant outcomes in kidney transplantation by incorporating the novel insights of donor-specific anti-HLA antibody (DSA) characteristics. The detection of anti-HLA DSA is widely used for the assessment of pre- and posttransplant risks of rejection and allograft loss; however, not all anti-HLA DSA carry the same risk for transplant outcomes. These antibodies have been shown to cause a wide spectrum of effects on allografts, ranging from the absence of injury to indolent or full-blown acute antibody-mediated rejection. Consequently, the presence of circulating anti-HLA DSA does not provide a sufficient level of accuracy for the risk stratification of allograft outcomes. Enhancing the predictive performance of anti-HLADSA is currently one of the most pressing unmet needs for facilitating individualized treatment choices that may improve outcomes. Recent advancements in the assessment of anti-HLADSA properties, including their strength, complement-binding capacity, and IgG subclass composition, significantly improved the risk stratification model to predict allograft injury and failure. Although risk stratification based on anti-HLA DSA properties appears promising, further specific studies that address immunological risk stratification in large and unselected populations are required to define the benefits and cost-effectiveness of such comprehensive assessment prior to clinical implementation.
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页数:8
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