Letvin N L, Chalifoux L V, Reimann K A, Ritz J, Schlossman S F, Lambert J M
J Clin Invest. 1986 Sep;78(3):666-73. doi: 10.1172/JCI112625.
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.
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缀合物在体内向淋巴结和脾脏中的T细胞的选择性递送。在输注未缀合的抗T11后,健康恒河猴的淋巴结和脾脏中的所有T淋巴细胞可实现短暂包被。由于衍生化抗体的清除比未缀合抗体更快,因此有必要输注比单独抗体更高剂量的免疫毒素,以实现抗T11对淋巴细胞结合位点的饱和。当输注足够的抗体-毒素缀合物时,输注后16小时在淋巴结和脾脏T细胞上很容易检测到毒素。毒素能够成功地特异性递送至猴体内的靶T细胞群体,这一结果表明在体内杀伤受限细胞群体应该是可行的。