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Effect of tumor necrosis factor-alpha and interleukin-2 on spleen lymphocyte migration in mouse skin.

机译:肿瘤坏死因子-α和白介素-2对小鼠皮肤脾淋巴细胞迁移的影响。

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Tumor necrosis factor-alpha (TNF-alpha) and interleukin-2 (IL-2) are reported to enhance lymphocyte binding to endothelial cells in vitro. We examined these two agents on lymphocyte migration in vivo. Spleen lymphocytes were radiolabeled with tritiated uridine (3H-UR) and then injected i.v. into mice. Each cytokine (TNF-alpha or IL-2) or both cytokines were then injected intradermally on the back of mice. The results demonstrated that TNF-alpha stimulates lymphocyte migration in vivo in dose-dependent fashion. Kinetic analysis demonstrated that migration with TNF-alpha started at 3 h, peaked at 6 h, followed by a gradual decline back to baseline at 24 h. IL-2, on the other hand, was nearly inactive, and did not augment lymphocyte migration over and above that induced by TNF-alpha when both cytokines were injected together.
机译:据报道,肿瘤坏死因子-α(TNF-α)和白介素2(IL-2)在体外可增强淋巴细胞与内皮细胞的结合。我们检查了这两种试剂对体内淋巴细胞迁移的影响。用tri化尿苷(3H-UR)对脾淋巴细胞进行放射性标记,然后静脉内注射。进入老鼠。然后将每种细胞因子(TNF-α或IL-2)或两种细胞因子皮内注射到小鼠背部。结果证明,TNF-α以剂量依赖性方式刺激体内淋巴细胞迁移。动力学分析表明,TNF-α的迁移在3 h开始,在6 h达到峰值,然后在24 h逐渐下降回到基线。另一方面,当将两种细胞因子一起注射时,IL-2几乎是无活性的,并且不会增加淋巴细胞的迁移,而不会超过TNF-α诱导的淋巴细胞迁移。

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