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机构地区:[1]长治市第二人民医院皮肤科,山西长治046000 [2]太原市中心医院皮肤科,山西太原030009
出 处:《临床皮肤科杂志》2008年第4期207-209,共3页Journal of Clinical Dermatology
基 金:国家自然科学基金(30771940);山西省自然科学基金(20031110);太原市科技局基金(0503044)资助项目
摘 要:目的:探讨造血细胞与银屑病患者CD4+ CD25+调节性T细胞活性异常的关系。方法:在胸腺基质细胞支持下,将骨髓CD34+细胞向T细胞定向分化,免疫磁珠法分离CD4+ CD25+调节性T细胞,分别在自然增殖状态及链球菌超抗原刺激下,采用四甲基偶氮唑蓝(MTT)法和ELISA法测定定向分化的CD4+ CD25+ T细胞增殖活性及分泌细胞因子水平。结果:在自然增殖状态下,银屑病患者CD34+细胞定向分化的CD4+ CD25+ T细胞显示与正常对照相似的增殖活性及白介素(IL)-2、IL-4、IL-8、IL-10、干扰素(IFN)-γ等细胞因子分泌水平,然而,在受到A族链球菌超抗原刺激后,银屑病患者定向分化的CD4+ CD25+ T细胞较正常对照显示相对低的增殖活性及分泌IL-2、IL-10能力。结论:银屑病患者CD34+细胞定向分化的CD4+ CD25+ T细胞功能异常,提示银屑病患者调节性T细胞功能异常可能源自遗传背景决定的骨髓造血细胞活性。Objectives: To confirm the hypothesis that hematopoietic stem cells are responsible for dysfunctional CD4^+CD25^+ regulatory cells in psoriasis. Methods: Bone marrow-derived CD34^+ hematopoietic cells from psoriatic patients with family history and normal control were differentiated to T cells in vitro. CD4^+CD25^+ T cells were isolated by immunomagnetic beads, and furthermore proliferation activity and capacity of secreting cytokines were determined by MTT and ELISA. Results: The differentiated CD4^+CD25^+ T cells of psoriatic origin showed similar characteristics to those of normal volunteers, including pro- liferation, secreting profile of cytokines (IL-2, IL-4, IL-8, IL-10 and IFN-γ). However, proliferation and levels of cytokines IL-2, IL-10 from CD4^+CD25^+ cells of psoriatic CD34^+ cells origin were significantly lower than those of normal control in response to Strep-A. Conclusions: CD4^+CD25^+ T cells differentiated in vitro from hematopoietic cells of psoriasis patients are impaired in the regulatory functions. It suggests the dysfunction of psoriatic CD4^+CD25^+ T cells due to an inherent genetic programming passed down from bone marrow hematopoietic cells.
关 键 词:银屑病 CD34^+细胞 造血细胞 T淋巴细胞 调节性T细胞
分 类 号:R758.63[医药卫生—皮肤病学与性病学]
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