首页> 美国卫生研究院文献>The Journal of Clinical Investigation >In vivo administration of lymphocyte-specific monoclonal antibodies in nonhuman primates. Delivery of ribosome-inactivating proteins to spleen and lymph node T cells.
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In vivo administration of lymphocyte-specific monoclonal antibodies in nonhuman primates. Delivery of ribosome-inactivating proteins to spleen and lymph node T cells.

机译:非人灵长类动物体内淋巴细胞特异性单克隆抗体的体内给药。将核糖体失活蛋白递送至脾和淋巴结T细胞。

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摘要

The selective delivery in vivo of a T lymphocyte-specific monoclonal antibody and immunotoxin conjugates to T cells in lymph node and spleen was assessed in rhesus monkeys. A transient coating of all T lymphocytes in the lymph nodes and spleens of healthy rhesus monkeys could be achieved after infusion of unconjugated anti-T11. Because derivatized antibody is cleared more rapidly than unconjugated antibody, it was necessary to infuse a higher dose of immunotoxin than antibody alone to achieve saturation of the lymphocyte binding sites with anti-T11. When sufficient antibody-toxin conjugate was infused, toxin was readily demonstrable on lymph node and spleen T cells by 16 h after infusion. This demonstration that toxins can be successfully delivered with specificity to target T cell populations in the monkey suggests that killing of restricted cell populations in vivo should be feasible.
机译:在恒河猴中评估了T淋巴细胞特异性单克隆抗体和免疫毒素偶联物向淋巴结和脾脏中T细胞的体内选择性递送。输注未结合的抗T11抗体后,即可获得健康恒河猴的淋巴结和脾脏中所有T淋巴细胞的瞬时涂层。由于衍生抗体的清除速度比未结合抗体的清除速度更快,因此有必要注入比单独抗体更高剂量的免疫毒素,以使抗T11的淋巴细胞结合位点达到饱和。当注入足够的抗体-毒素结合物时,在注入后16 h内,淋巴结和脾T细胞上的毒素很容易被证实。毒素可以特异性地成功递送到猴子中的靶T细胞群体的这一证明表明,体内杀死限制性细胞群体应该是可行的。

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