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TREATMENT OF FIBROSIS WITH GENETICALLY-ENGINEERED MACROPHAGES

机译:近因工程巨噬细胞治疗纤维化

摘要

Provided herein are macrophages engineered for treating fibrosis and ameliorating the effects of fibrotic lesions in various organs and tissues. Certain embodiments are directed to genetically-engineered macrophages capable of treating fibrosis or reducing fibrotic lesions. In certain aspects macrophages can be genetically-engineered to (1) target extracelluar matrix (ECM) or components thereof, (2) enhance degradation of ECM, or (3) target ECM and enhance degradation of ECM. Further provided is a cellular therapy product comprising a genetically-engineered macrophage comprising at least one of a recombinant targeting protein and a recombinant catalytic enzyme. Further provided is a method of treating an individual for fibrosis comprising administering the cellular therapy product.
机译:本文提供了用于治疗纤维化和改善各种器官和组织中纤维化病变的影响的巨噬细胞。 某些实施方案涉及能够治疗纤维化或减少纤维化病变的遗传工程巨噬细胞。 在某些方面,巨噬细胞可以遗传地设计为(1)靶细胞外基质(ECM)或其组分,(2)增强ECM的降解,或(3)靶ECM并增强ECM的降解。 进一步提供的是细胞治疗产品,其包含遗传工程巨噬细胞,其包含至少一种重组靶向蛋白和重组催化酶。 进一步提供的是治疗纤维化的个体的方法,包括给予细胞治疗产品。

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