Cell regeneration medicine in case of salih myopathy and hypoxic encephalopathyhy

Felipe Torres Obando, J. M. Velasco, N. Soto, D. Vergara
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Abstract

(GW) have low immunogenicity due to the fact that they do not activate the proliferation of T cells, as they do not express the main histocompatibility complex class II (MHCII) or the cd40, cd80 and cd86 molecules, necessary for the activation of t cells.3 The world literature has not shown that when CMMGW is administered, the proliferation of lymphocytes is suppressed and also does not activate mhc20. For this reason, rejection after cell graft transplantation is minimal or null, even among individuals without any consanguinity.4 Another beneficial effect is that MSCs have an immunomodulatory effect on T and B lymphocytes, dendritic cells and NK cells, since it can inhibit the proliferation of immune cells and reduce the secretion of cytokines and the presence of the subtypes of cells infiltrated in tissue.3,5–8 which attenuates inflammation and promotes wound healing. These characteristics and properties of allogeneic CMMGW provide an advantage for tissue regeneration and thus achieve wound closure and avoid rejection.9–12
唾液性肌病和缺氧性脑病的细胞再生药物
(GW)具有较低的免疫原性,因为它们不表达激活T细胞所必需的主要组织相容性复合体II类(MHCII)或cd40、cd80和cd86分子,因此它们不激活T细胞的增殖国际文献尚未表明,当CMMGW被施用时,淋巴细胞的增殖受到抑制,也不激活mhc20。因此,即使在没有任何血缘关系的个体中,细胞移植后的排斥反应也很少或完全没有另一个有益的作用是MSCs对T淋巴细胞和B淋巴细胞、树突状细胞和NK细胞具有免疫调节作用,可以抑制免疫细胞的增殖,减少细胞因子的分泌,减少组织中浸润细胞亚型的存在。3,5 - 8,减轻炎症,促进伤口愈合。同种异体CMMGW的这些特性和特性为组织再生提供了优势,从而实现伤口愈合和避免排斥反应
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