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J Osawa
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引用次数: 0

摘要

采用抗原特异性淋巴细胞增殖试验(LPT)研究了巯基药物致敏小鼠淋巴细胞(LNC)对重组白细胞介素2 (il -2)的反应。用硫普罗宁(TP)和硫硫酸金钠(GTM)对小鼠进行体外培养,观察其对LNC的二次反应。采用碘化丙啶快速荧光显色法(RFP)代替3h -胸腺嘧啶摄取法定量测定LPT。TP或gtm引物的LNC对特异性抗原的增殖反应与对照无显著差异。与此相反,当致敏小鼠的LNC与致敏抗原和rIL-2一起培养时,可以观察到明显的增殖。反应的强度取决于il -2的浓度。我们认为在TP或gtm致敏小鼠的LPT中添加IL-2可增强抗原特异性淋巴细胞增殖反应,采用RFP法测定IL-2的反应性可能有助于检测人体巯基药物过敏。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[IL-2 responsiveness in antigen-specific lymphocyte proliferation test with sulfhydryl drug-sensitized murine lymphocytes--using rapid fluorochromasia assay].

Response of murine lymphnode cells (LNC) sensitized with sulfhydryl drugs to recombinant interleukin 2 (rIL-2) was studied in antigen-specific lymphocyte proliferation test (LPT). Mice were primed with tiopronin (TP) and gold sodium thiomalate (GTM) and the secondary response to LNC was measured in a proliferative assay in vitro. Rapid fluorochromasia assay with propidium iodide (RFP) was used for the quantitative measurement of LPT instead of 3H-thymidine uptake. There was no difference in proliferative response to specific antigen between TP or GTM-primed LNC and control ones. In contrast, a significant proliferation was observed when LNC from sensitized mice were cultured with sensitizing antigen and rIL-2. The strength of response was dependent on the concentration of rIL-2. It was considered that adding rIL-2 to LPT of TP or GTM-sensitized mice enhanced antigen-specific lymphocyte proliferative response and the measurement of IL-2 responsiveness using RFP method might be useful to detect sulfhydryl drug allergy in man.

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