细胞壁的免疫佐剂活性,它们的水溶性组分和肽聚糖亚基,由各种革兰氏阳性菌和合成的n-乙酰muramyl肽制备。

S Kotani, Y Watanabe, T Shimono, T Narita, K Kato
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引用次数: 0

摘要

1. 大约20种革兰氏阳性细菌的细胞壁,除了少数例外,被发现在刺激血清抗体水平增加和诱导卵蛋白延迟型超敏反应时,以油包水乳剂的形式给药给豚鼠时,绝对具有佐剂活性。2. 通过使用多种细胞壁裂解酶,免疫佐剂原理被溶解,在金黄色葡萄球菌、化脓性链球菌、变形链球菌、植物乳杆菌、白喉链球菌、Myc的细胞壁上观察到佐剂活性的完全保留。耻毛苔和粘毛苔。n -乙酰muramyl肽单体(L-Lys或中位磷酸二酶型)被证明是负责佐剂活性表现的单位化学结构,以刺激抗体介导和细胞介导的免疫反应。3.采用双环己基碳二亚胺- n -羟基琥珀酰亚胺法制备了n -乙酰基-4,6- o -苄基- -muramide苄酯和各肽苄酯缩合,氢解去除保护基团,制备了几种n -乙酰基muramyl肽。n -乙酰muramyl- l- alanyl- d -异谷氨酰胺被确定为细菌细胞壁免疫佐剂活性特征所必需的最小结构实体。合成的n -乙酰muramyl- l-丙氨酸和l- alanyl- d -异谷氨酰基-l -赖氨酸- d -丙氨酸都没有活性。
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Immunoadjuvant activities of cell walls, their water-soluble fractions and peptidoglycan subunits, prepared from various gram-positive bacteria, and of synthetic n-acetylmuramyl peptides.

1. The cell walls from some 20 species of gram-positive bacteria, with only few exceptions, were found to be definitely adjuvant-active in both stimulation of increased serum antibody levels and induction of delayed-type hypersensitivity to ovalbumin when administered to guinea pigs in the form of a water-in-oil emulsion. 2. By the use of various cell wall lytic enzymes, the immunoadjuvant principles were solubilized with the full retention of adjuvant activities observed with the cell walls of S. aureus, Str. pyogenes, Str. mutans, L. plantarum, C. diphtheriae, Myc. smegmatis and A. viscosus. N-acetylmuramyl peptide monomers (either L-Lys or meso-Dap type) were shown to be the unit chemical structure responsible for the manifestation of adjuvant activities to stimulate both antibody-mediated and cell-mediated immune responses. 3. Several N-Acetylmuramyl peptides were prepared by condensation of benzyl N-acetyl-4,6-O-benzylidene-alpha-muramide with each peptide benzyl ester by means of dicyclohexylcarbodiimide-N-hydroxysuccinimide method and removal of the protecting groups by hydrogenolysis. N-acetylmuramyl-L-alanyl-D-isoglutamine was identified as the minimum structural entity essential for the immunoadjuvant activities characteristic of bacterial cell walls. Neither synthetic N-acetylmuramyl-L-alanine nor L-alanyl-D-isoglutaminyl-L-lysyl-D-alanin was found to be active.

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