肽聚糖佐剂:活性所需的最小结构。

A Adam, F Ellouz, R Ciorbaru, J F Petit, E Lederer
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引用次数: 0

摘要

研究了分枝杆菌细胞壁佐剂活性组分的化学结构。以前已经证明,通过溶菌酶消化或其他处理从分枝杆菌细胞壁获得的可溶性肽聚糖片段可作为佐剂,增强体液和细胞免疫。然后我们发现分枝杆菌的肽聚糖(即双糖四肽)的单体亚基具有佐剂活性;然后,对来自其他菌株的类似化合物进行了测试;发现中二氨基亚酸单体亚基和含有肽聚糖的l -赖氨酸具有辅助活性。目前研究的最小的活性化合物是SINAY et al.(1975)为我们合成的N-acetyl-muramyl-L-alanyl-D-isoglutamine。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peptidoglycan adjuvants: minimal structure required for activity.

The chemical structure of the adjuvant active fraction of mycobacterial cell walls has been investigated. It had been shown previously that soluble peptidoglycan fragments obtained from cell walls of Mycobacteria by lysozyme digestion or by other treatments act as adjuvants for increasing both humoral and cellular immunity. We then found that even the monomer subunit of the peptidoglycan of Mycobacteria (i.e. a disaccharide-tetrapeptide) is adjuvant active; then, similar compounds from other strains of bacteria were tested; the monomeric subunits of meso-diaminopimelic acid as well as L-lysine containing peptidoglycans were found to be adjuvant active. The smallest active compound studied so far is N-acetyl-muramyl-L-alanyl-D-isoglutamine synthesized for us by SINAY et al. (1975).

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