Chisholm P L, Williams C A, Jones W E, Majeau G R, Oleson F B, Burrus-Fischer B, Meier W, Hochman P S
Biogen, Cambridge, MA 02142, USA.
Ther Immunol. 1994 Aug;1(4):205-16.
LFA3TIP, a fusion protein comprised of the first extracellular domain of LFA-3 fused to the hinge, CH2 and CH3 domains of human IgG1, inhibits proliferation of human T cells in vitro. LFA3TIP also inhibits responses of human CD2 transgenic mice by rapidly and totally depleting peripheral T cells. These effects require binding of the LFA-3 and CH2 domains of LFA3TIP to CD2+ T cells and Fc gamma R+ accessory cells, respectively. As CD2 is well conserved in primate species, we evaluated the effects of LFA3TIP in nonhuman primates. We report in vitro results leading to the selection of the baboon as a model for analysis of LFA3TIP, and in vivo effects of single and multidose regimens of LFA3TIP administration. This is the first report of the in vivo administration of an immunomodulatory fusion protein to primates. LFA3TIP is shown to mediate effects on primate T lymphocytes without apparent related toxicities or immunogenicity. Results are discussed in context of potential mechanisms of LFA3TIP immunotherapy.
LFA3TIP是一种融合蛋白,由LFA - 3的第一个细胞外结构域与人IgG1的铰链区、CH2和CH3结构域融合而成,在体外可抑制人T细胞的增殖。LFA3TIP还可通过快速、完全清除外周T细胞来抑制人CD2转基因小鼠的反应。这些效应分别需要LFA3TIP的LFA - 3和CH2结构域与CD2 + T细胞和FcγR + 辅助细胞结合。由于CD2在灵长类动物中高度保守,我们评估了LFA3TIP在非人类灵长类动物中的作用。我们报告了体外实验结果,这些结果促使选择狒狒作为分析LFA3TIP的模型,以及LFA3TIP单剂量和多剂量给药方案的体内效应。这是首次关于向灵长类动物体内施用免疫调节融合蛋白的报告。结果显示LFA3TIP可介导对灵长类T淋巴细胞的作用,且无明显相关毒性或免疫原性。本文结合LFA3TIP免疫治疗的潜在机制对结果进行了讨论。