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恶性肿瘤胸腹水中TIL生物学活性研究

Study on biological activity of TIL from malignant pleursl effusion and ascites and the regulation of its killing activity
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摘要 从卵巢癌腹水和肺癌胸水中分离出肿瘤浸润淋巴细胞(TIL),用rIL-2诱导培养,观察其增殖活性。同时观察了PJ-CW、POGP、PHA等对其杀伤活性的调节作用。结果表明,在培养5~10天时TIL增殖较快,其表面产生的CD3、CD4、CD8、Tac等抗原,随培养时间的延长,表达量增加,尤以CD8增加较明显,CD4/CD8比值逐降。其表面产生的HLA-DR、HLA-ABC抗原,在培养15天内有增加表现,以后下降。其杀伤活性在培养5~10天较高,其后活性下降。在培养系统中加入PJ-CW、POGP、PHA等后,培养5天时,TIL杀伤活性分别为82.70%,85.50%,84.35%(对照组为内保持较高的杀伤活性。 Tumor infiltration lymphocytes (TIL) were separated from ovary cancer ascites and lung cancer pleural effusion , and cultured with rlL -2. We observed the dynamics of its proliferation activity , production of surface antigens and killing activity ,in addition ,the regulation effect of PJ-CW ,POGP ,PHA on the killing activity of TIL we were also observed. It showed iT IL proliferated fast at culture for 5-10 days , with prolongation of the culture time ,production of CD3 , 4 , 8 ,Tac antigen ,especially CD8 increased ,so the ratio of CD4 /CD8 decreased gradually. The production of HLA -DR , HLA-ABC antigens increased within culture for 15 days , and then decreased . The killing activity increased and reached the top at culture for 5 days ,and then decreased. Adding PJ-CW ,POGP and PHA into the culture medium , the killing activity of TIL at culture for 5-10 days was 82.70% , 85.50% and 84. 35% respectively ,higher than that of control (66. 80%) obviously, and maintained higher killing activity within 20 days.
出处 《中华微生物学和免疫学杂志》 CAS CSCD 北大核心 1996年第3期168-170,共3页 Chinese Journal of Microbiology and Immunology
关键词 肿瘤浸润 淋巴细胞 胸腹水 肿瘤 生物活性 Tumor infiltration cymphocytes (TIL) PJ-CW POGP PHA Killing activity
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