首页> 外国专利> PROCESS AND SYSTEM FOR GENETIC AND EPIGENETIC IN VITRO REPROGRAMMING OF CELLS AND USE OF A REPROGRAMMED CELL IN THE PREPARATION OF A PHARMACEUTICAL COMPOSITION

PROCESS AND SYSTEM FOR GENETIC AND EPIGENETIC IN VITRO REPROGRAMMING OF CELLS AND USE OF A REPROGRAMMED CELL IN THE PREPARATION OF A PHARMACEUTICAL COMPOSITION

机译:遗传和表位的细胞体外重编程的过程和系统,以及在医药组合物的制备中使用重编程的细胞

摘要

The invention relates to an epigenetic and genetic treatment method and system. The invention can be used to rejuvenate an adult cell nucleus without passing through an embryonic stage and to obtain a tissue that is genetically-rejuvenated and autologous in relation to the original nucleus, comprising the temporary introduction of a nucleus into an enucleated oocyte (genetic rejuvenation), followed by oocyte extraction prior to cell division. The treated nucleus can then be introduced into an adult cytoplasm originating from the nucleus. In this way, cell divisions from the rejuvenated nucleus take place in an adult autologous cytoplasm and the resulting cells immediately take the form of adult, differentiated and functional cells. The rejuvenated autologous tissue thus created can then be grafted without rejection to the adult tissue of the organism from the treated nucleus. Throughout the inventive procedure, the treated cytoplasms and nuclei remain permanently in the adult state and no artificial cell differentiation is necessary. In this way, the invention is different from standard deep cloning in which the treated cells must return to the embryonic stage and which involves artificial cell differentiation. In addition, the tissues derived from standard cloning are not immunologically compatible with the original adult tissues from the treated nucleus since the cell division thereof takes place in the oocyte which represents a foreign cytoplasm to the nucleus. Moreover, standard cloning enables the creation of whole organisms unlike the inventive method and system which can only be used to treat a single tissue. The possible applications of the invention include, for example, the repair of necrotic tissues, such as a myocardial infarction, and damaged tissues, such as the retina (RMD), heart failure, renal failure, liver failure and osteoporosis, the treatment of cancers that occur with age, such as prostate cancer, rectal cancer, colon cancer, etc. The anodyne implantation of a small volume of autologous, rejuvenated, still-healthy cells from the affected organ should inhibit the aforementioned cancers and the metastases thereof.
机译:本发明涉及表观遗传治疗方法和系统。本发明可用于使成年细胞核恢复活力而不经过胚胎期,并且获得与原始细胞核有关的基因被恢复活力和自体的组织,包括将细胞核暂时引入去核的卵母细胞(遗传回春)。 ),然后在细胞分裂之前先进行卵母细胞提取。然后可以将处理过的细胞核引入起源于细胞核的成年细胞质中。以这种方式,在新生的自体细胞质中发生了从新生核的细胞分裂,并且所得的细胞立即采取了成年的,分化的和功能性细胞的形式。然后,可以将由此产生的再生的自体组织移植,而不会从处理过的核排斥到生物体的成年组织。在整个发明过程中,处理过的细胞质和细胞核永久保持成年状态,不需要人工细胞分化。以此方式,本发明不同于标准的深克隆,在深度的深克隆中,被处理的细胞必须返回到胚胎阶段,并且涉及人工细胞分化。另外,源自标准克隆的组织与来自经处理的核的原始成年组织在免疫学上不相容,因为其细胞分裂发生在卵母细胞中,卵母细胞代表了细胞核的外来细胞质。此外,与仅可用于治疗单个组织的发明方法和系统不同,标准克隆能够创建整个生物体。本发明的可能应用包括例如修复坏死组织,例如心肌梗塞和受损组织,例如视网膜(RMD),心力衰竭,肾衰竭,肝衰竭和骨质疏松症,癌症的治疗。随着年龄的增长,前列腺癌,直肠癌,结肠癌等会随着年龄的增长而发生。从受影响的器官以少量的自体,再生的,仍然健康的细胞进行止痛剂植入,应能抑制上述癌症及其转移。

著录项

  • 公开/公告号IL186988A

    专利类型

  • 公开/公告日2011-12-29

    原文格式PDF

  • 申请/专利权人 FRED ZACOUTO;

    申请/专利号IL20070186988

  • 发明设计人

    申请日2007-10-29

  • 分类号C12N5/075;

  • 国家 IL

  • 入库时间 2022-08-21 17:24:49

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