期刊文献+

疣毒净对复发性尖锐湿疣患者淋巴细胞凋亡调控蛋白的影响 被引量:2

The influence of Youdujing on lymphocyte apoptosis-modulated protein in recurrent condyloma acuminatum
下载PDF
导出
摘要 目的 : 观察中药疣毒净系列制剂对复发性尖锐湿疣患者淋巴细胞凋亡调控蛋白的影响。方法 : 选择经疣毒净系列制剂治疗前、后复发性尖锐湿疣患者血液行淋巴细胞凋亡调控蛋白Bcl - 2、CD95 + 、CD95L的检测并与健康人群进行对照。结果 : 复发性尖锐湿疣患者治疗前后CD95 + 、CD95L表达水平高于健康对照组 ,Bcl- 2则低于健康对照组 (P<0 .0 5 ) ,而治疗前组CD95 + 、CD95L表达水平分别高于治疗后组 (P <0 .0 5 ) ,Bcl- 2则低于治疗后组 (P <0 .0 1)。结论 Objective: To determine the influence of lymphocyte apoptosis-modulated protein in the patients with recurrent condyloma acuminatum (CA) treated with Youdujing (YDJ). Methods: Apoptosis modulated proteins Bcl-2, CD95 + and CD95L were detected in the patients with recurrent CA before and after treatment with YDJ and compared with normal controls.Results: Before or after the treatment with YDJ, the expressions of CD95 + and CD95L was higher in patients with recurrent CA than that in normal controls while the expression of Bcl-2 was lower in the patients than that in normal controls (P<0.05). In addition, the expression of CD95 + and CD95L was higher before the treatment with YDJ than that after the treatment with YDJ (P<0.05), while the expression of Bcl-2 was higher after treatment than that before treatment (P<0.01). Conclusion : The ability of anti-apoptosis has significantly increased in the patients treated with YDJ.
出处 《中国麻风皮肤病杂志》 北大核心 2003年第6期553-554,共2页 China Journal of Leprosy and Skin Diseases
基金 广东省自然科学基金题 (编号 :0 0 356)
  • 相关文献

参考文献4

二级参考文献5

  • 1肖嵘,王仁林,张运昌.尖锐湿疣患者外周血淋巴细胞表型及治疗后的变化[J].中国皮肤性病学杂志,1995,9(4):204-204. 被引量:56
  • 2肖嵘,中国皮肤性病学杂志,1995年,9卷,204页
  • 3Thompson CB.Apoptosis in the pathogenesis and treatment of disease[J],1995(5203).
  • 4Cauda R;Tyring SK;Grossi CE.Patients with condyloma acuminatum exhibit decreased interleukin- 2 and interferon gamma production and depressed natural killer activity[J],1987.
  • 5Yared G;Hussain KB;Nathani MG.Cytokine- mediated apoptosis and inhibition of virus production and anchorage independent growth of viral transfected hepatoblastoma cells[J],1998.

共引文献236

同被引文献14

引证文献2

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部