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α-羟乙酰神经氨酸(Neu5Gc)末端聚糖的结构复杂性与动物组织分布。对其在临床异种移植中免疫原性的影响。

The Structural Complexity and Animal Tissue Distribution of -Glycolylneuraminic Acid (Neu5Gc)-Terminated Glycans. Implications for Their Immunogenicity in Clinical Xenografting.

作者信息

Breimer Michael E, Holgersson Jan

机构信息

Department of Surgery, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Laboratory Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Front Mol Biosci. 2019 Jul 19;6:57. doi: 10.3389/fmolb.2019.00057. eCollection 2019.

Abstract

-Glycolylneuraminic acid (Neu5Gc)-terminated glycans are present in all animal cells/tissues that are already used in the clinic such as bioprosthetic heart valves (BHV) as well as in those that potentially will be xenografted in the future to overcome end stage cell/organ failure. Humans, as a species lack this antigen determinant and can react with an immune response after exposure to Neu5Gc present in these products/cells/tissues. Genetically engineered source animals lacking Neu5Gc has been generated and so has animals that in addition lack the major αGal xenoantigen. The use of cells/tissues/organs from such animals may improve the long-term performance of BHV and allow future xenografting. This review summarizes the present knowledge regarding structural complexity and tissue distribution of Neu5Gc on glycans of cells/tissue/organs already used in the clinic or intended for treatment of end stage organ failure by xenografting. In addition, we briefly discuss the role of anti-Neu5Gc antibodies in the xenorejection process and how knowledge about Neu5Gc structural complexity can be used to design novel diagnostics for anti-Neu5Gc antibody detection.

摘要
  • 糖基化神经氨酸(Neu5Gc)末端聚糖存在于所有已用于临床的动物细胞/组织中,如生物人工心脏瓣膜(BHV),以及那些未来可能用于异种移植以克服终末期细胞/器官衰竭的细胞/组织中。作为一个物种,人类缺乏这种抗原决定簇,在接触这些产品/细胞/组织中存在的Neu5Gc后可能会产生免疫反应。已经培育出了缺乏Neu5Gc的基因工程源动物,也培育出了同时缺乏主要αGal异种抗原的动物。使用来自此类动物的细胞/组织/器官可能会改善BHV的长期性能,并为未来的异种移植创造条件。这篇综述总结了目前关于Neu5Gc在已用于临床或旨在通过异种移植治疗终末期器官衰竭的细胞/组织/器官聚糖上的结构复杂性和组织分布的知识。此外,我们简要讨论了抗Neu5Gc抗体在异种排斥过程中的作用,以及关于Neu5Gc结构复杂性的知识如何用于设计检测抗Neu5Gc抗体的新型诊断方法。

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