最佳认知距离和吸收能力

B. Nooteboom, W. Vanhaverbeke, G. Duysters, V. Gilsing, A. van den Oord
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引用次数: 1367

摘要

本申请涉及一种通过识别阻断CD4和MHC (II类)基因产物相互作用的化合物来识别可用于抑制不想要的人CD4 T细胞免疫反应的化合物的方法,以及一种包括施用这种已识别化合物的治疗方法。抑制不希望的人类CD4 T细胞免疫反应的化合物可用于治疗疾病,如多发性硬化症和预防移植物排斥和移植物抗宿主病。更具体地说,该申请涉及分子量在1400至400之间的化合物,其模拟人类CD4淋巴细胞表面抗原的三个部分。部分为D1结构域的C-C′环残基29-35;残基317-323为D4结构域的C-C′环;和残基346-353,CD4分子D4结构域的CDR3或FG脊。这类化合物的具体实例包括环肽和拟肽。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimal Cognitive Distance and Absorptive Capacity
The application concerns a method of identifying compounds that can be used to inhibit undesired human CD4 T cell immune responses by identifying compounds that block the interaction of CD4 and MHC, class II, gene products and a method of treatment which comprises administering such an identified compound. The compounds that inhibit undesired human CD4 T cell immune responses can be used to treat disease such as multiple sclerosis and to prevent graft rejection and graft versus host disease. More specifically, the application concerns compounds having molecular weights between about 1400 and 400 that mimic three portions of the human CD4 lymphocyte cell surface antigen. The portions are residues 29-35, the C-C' loop of the D1 domain; residues 317-323, the C-C' loop of the D4 domain; and residues 346-353, the CDR3 or FG ridge of the D4 domain of the CD4 molecule. Specific examples of such compounds include cyclic peptides and peptidomimetic.
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