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骨髓增生异常综合征患者中红系祖细胞(BFU-E)的体外生长及T淋巴细胞爆式促进活性(BPA)的产生。

In vitro growth of erythroid progenitor cells (BFU-E) and production of burst-promoting activity (BPA) by T lymphocytes in patients with myelodysplastic syndromes.

作者信息

Morra L, Moccia F, Ponassi I, Bessone G, Mela G S, Ponassi G A

机构信息

Dipartimento di Medicina Interna, Università di Genova, Italy.

出版信息

Biomed Pharmacother. 1992;46(9):393-9. doi: 10.1016/0753-3322(92)90043-7.

Abstract

The in vitro growth of circulating erythroid progenitors (BFU-E) populations and the production of burst-promoting activity (BPA) by T lymphocytes have been studied in 17 patients with myelodysplastic syndromes. Based on the in vitro growth patterns of BFU-E, four groups of patients have been identified: i) normal BFU-E growth; ii) low spontaneous BFU-E growth, but normal response to LCM; iii) impaired BFU-E response to LCM; iv) no BFU-E growth. The pattern of BFU-E growth seems to be related to the clinical stage of the disease rather than to the FAB subgroup to which the patients belong. The ability of T lymphocytes to stimulate BFU-E growth was significantly reduced in all patients. The possible mechanisms inducing the impaired production of BPA by T lymphocytes are discussed. The in vitro evaluation of circulating erythroid precursors can supply useful prognostic information and possibly indications concerning the responsiveness of erythropoietic stem cells to recombinant human erythropoietin in vivo.

摘要

对17例骨髓增生异常综合征患者的循环红系祖细胞(BFU-E)群体的体外生长情况以及T淋巴细胞产生爆式促进活性(BPA)的情况进行了研究。根据BFU-E的体外生长模式,已将患者分为四组:i)BFU-E生长正常;ii)自发BFU-E生长低,但对LCM反应正常;iii)BFU-E对LCM反应受损;iv)无BFU-E生长。BFU-E的生长模式似乎与疾病的临床阶段有关,而非与患者所属的FAB亚组有关。所有患者中T淋巴细胞刺激BFU-E生长的能力均显著降低。讨论了导致T淋巴细胞产生BPA受损的可能机制。循环红系前体细胞的体外评估可为体内促红细胞生成干细胞对重组人促红细胞生成素的反应性提供有用的预后信息及可能的指征。

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