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人骨髓来源的基质祖细胞(间充质祖细胞)的体外扩增及随后的输注:对治疗应用的意义。

Ex vivo expansion and subsequent infusion of human bone marrow-derived stromal progenitor cells (mesenchymal progenitor cells): implications for therapeutic use.

作者信息

Lazarus H M, Haynesworth S E, Gerson S L, Rosenthal N S, Caplan A I

机构信息

Department of Medicine, Ireland Cancer Center of University Hospitals of Cleveland, Case Western Reserve University, Ohio 44106, USA.

出版信息

Bone Marrow Transplant. 1995 Oct;16(4):557-64.

PMID:8528172
Abstract

We report a phase I trial to determine the feasibility of collection, ex vivo culture-expansion and intravneous infusion of human bone marrow-derived progenitor stromal cells (mesenchymal progenitor cells (MPCs)). Ten milliliter bone marrow samples were obtained from 23 patients with hematologic malignancies in complete remission. Bone marrow mononuclear cells were separated and adherent cells were culture-expanded in vitro for 4-7 weeks. Autologous MPCs were reinfused intravenously and a bone marrow examination repeated 2 weeks later for histologic assessment and in vitro hematopoietic cultures. Patient age ranged from 18 to 68 years and 12 subjects previously had undergone an autologous or syngeneic bone marrow transplant 4-52 months prior to collection of MPCs. A median of 364 x 10(6) nucleated bone marrow cells (range: 103 to 1004 x 10(6)) were used for ex vivo expansion. Median number of MPCs which were obtained after ex vivo culture expansion was 59.0 (range: 1.1 to 347 x 10(6)) representing a median cell doubling of 16,000-fold (13 doublings). Fifteen of 23 patients completed the ex vivo expansion and underwent MPC infusion. Time to infusion of MPCs after collection ranged from 28 to 49 days. Five patients in each of three groups were given 1, 10 and 50 x 10(6) MPCs. No adverse reactions were observed with the infusion of the MPCs. MPCs obtained from cancer patients can be collected, expanded in vitro and infused intravenously without toxicity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们报告了一项I期试验,以确定采集、体外培养扩增和静脉输注人骨髓来源的祖基质细胞(间充质祖细胞(MPCs))的可行性。从23例完全缓解的血液系统恶性肿瘤患者中获取10毫升骨髓样本。分离骨髓单个核细胞,贴壁细胞在体外培养扩增4 - 7周。将自体MPCs静脉回输,2周后重复进行骨髓检查以进行组织学评估和体外造血培养。患者年龄在18至68岁之间,12名受试者在采集MPCs前4 - 52个月曾接受过自体或同基因骨髓移植。用于体外扩增的有核骨髓细胞中位数为364×10⁶(范围:103至1004×10⁶)。体外培养扩增后获得的MPCs中位数为59.0(范围:1.1至347×10⁶),代表细胞中位数倍增16000倍(13次倍增)。23例患者中有15例完成了体外扩增并接受了MPCs输注。采集后至输注MPCs的时间为28至49天。三组中每组5例患者分别接受了1×10⁶、10×10⁶和50×10⁶个MPCs。输注MPCs未观察到不良反应。从癌症患者获得的MPCs可以采集、体外扩增并静脉输注且无毒性。(摘要截断于250字)

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