Shroff Geeta, Srivastav Arpita, Shroff Rohan
Nutech Mediworld, New Delhi, India.
Int J Stem Cells. 2018 May 30;11(1):105-110. doi: 10.15283/ijsc17064.
Human embryonic stem cells (hESCs) have the potential to treat various human disorders currently labeled as incurable and/or terminal illness. However, the fear that the patients' immune system would recognize them as non self and lead to an immune rejection has hampered their use. The main cause for immune rejection is usually the incompatibility of both donor and recipient's major histocompatibility complex (MHC).
We describe a hESC line developed through a patented technology that does not lead to immune reaction upon transplantation. We have transplanted these cells in >1,400 patients with chronic/terminal conditions and did not observe any immune reaction. No immunosuppressant were administered to these patients. We analyzed the expression levels of MHC-I and MHC-II on the surface of these hESCs using microarray technology. The gene targets for miRNA were analyzed using Gene ontology and DAVID database and pathways for these genes were determined using Reactome and Panther databases.
Our results showed that the levels of expression of MHC-I and MHC-II on hESCs is almost negligible and thus the hESCs are less susceptible to an immune rejection.
The hESCs cultured at our facility expresses low levels of MHC-I and do not produce an immune reaction. These can be administered universally and need no cross matching before transplantation.
人类胚胎干细胞(hESCs)有潜力治疗目前被列为无法治愈和/或绝症的各种人类疾病。然而,担心患者的免疫系统会将它们识别为非自身并导致免疫排斥反应,这阻碍了它们的应用。免疫排斥的主要原因通常是供体和受体的主要组织相容性复合体(MHC)不匹配。
我们描述了一种通过专利技术开发的hESC系,该系在移植后不会引发免疫反应。我们已将这些细胞移植到1400多名患有慢性/终末期疾病的患者体内,未观察到任何免疫反应。这些患者未使用免疫抑制剂。我们使用微阵列技术分析了这些hESCs表面MHC-I和MHC-II的表达水平。使用基因本体论和DAVID数据库分析了miRNA的基因靶点,并使用Reactome和Panther数据库确定了这些基因的途径。
我们的结果表明,hESCs上MHC-I和MHC-II的表达水平几乎可以忽略不计,因此hESCs较不易受到免疫排斥。
在我们的设施中培养的hESCs表达低水平的MHC-I,不会产生免疫反应。这些细胞可以普遍施用,移植前无需进行交叉配型。