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SARS患者T淋巴细胞亚群的改变及动态观察
引用本文:杨民,路遥,付琦,徐克沂. SARS患者T淋巴细胞亚群的改变及动态观察[J]. 中华微生物学和免疫学杂志, 2003, 23(12): 936-938
作者姓名:杨民  路遥  付琦  徐克沂
作者单位:100011,北京地坛医院
摘    要:目的 了解SARS患者T细胞亚群的改变及动态变化 ,探讨其发病机理及对预后的影响。方法 将住院 5 4例SARS患者分为治愈组 (31例 )与死亡组 (2 3例 )两组 ,用流式细胞仪进行T细胞亚群的动态观察。结果 治愈组与死亡组CD4 + 、CD8+ 均值在发病初的 15d内均显著低于正常值 ,死亡组更为显著 ,但两组比较P >0 .0 5 ,差异无显著性。发病 15d后治愈组CD4 + 、CD8+ 均值显著上升 ,而死亡组CD4 + 、CD8+ 均值持续低水平 ,两组比较P <0 .0 0 1,差异有非常显著性。治愈组早期 (≤15d)与后期 (>15d)CD4 + 、CD8+ 均值比较P <0 .0 0 1,差异有非常显著性。死亡组早期与后期CD4 + 、CD8+ 均值比较P >0 .0 5 ,差异无显著性。结论 SARS患者在发病初的 15d内细胞免疫功能是低下的。治愈组 15d后细胞免疫功能逐渐恢复正常 ,预后良好。而死亡组 15d后细胞免疫功能持续低水平 ,提示预后不良。发病的第 15天左右是疾病的转折点。CD4 + 值持续 <2 5 0 ,CD8+ 值持续 <2 0 0是预后不良的重要指标。

关 键 词:SARS T淋巴细胞亚群 动态观察 发病机理 预后 非典型肺炎
修稿时间:2003-06-28

Subsets of peripheral T lymphocyte in SARS patients
YANG Min,LU Yao,FU Qi,XU Ke-yi. Subsets of peripheral T lymphocyte in SARS patients[J]. Chinese Journal of Microbiology and Immunology, 2003, 23(12): 936-938
Authors:YANG Min  LU Yao  FU Qi  XU Ke-yi
Affiliation:YANG Min,LU Yao,FU Qi,XU Ke-yi. Beijing Ditan Hospital,Beijing 100011,China
Abstract:Objective To investigate the change of subsets of peripheral T lymphocyte in patients with severe acute respiratory syndrome (SARS) and their clinical significance. Methods Subsets of peripheral T lymphocyte from 54 patients with SARS (included 23 dead cases) were examined by flow cytometer. Results The numbers of both CD4 + and CD8 + lymphocytes were significantly decreased in acute phase (15 days) of SARS patients. No significant difference was found between dead and alive groups ( P >0.05). After 15 days of treatment the numbers of CD4 + and CD8 + lymphocytes of the alive cases were significantly increased and the in dead cases the numbers were still lower ( P <0.001). Conclusion The patients with SARS were found to have a damaged cellular immunity. The alive patients would recovered from the damage of cellular immunity after 15 days. The a poor prognosis would be expected if the number of CD4 + was persistantly lower then 250.
Keywords:Severe acute respiratory syndrome  T lymphocyte subsets
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