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合成去 muramyl 肽脂 Triglymyc 在小鼠和豚鼠体内免疫调节活性的比较。

Comparison of immunomodulatory activities in mice and guinea pigs of a synthetic desmuramyl peptidolipid triglymyc.

作者信息

Leclerc C D, Audibert F M, Chedid L A, Deriaud E J, Masihi N K, Lederer E

出版信息

Infect Immun. 1984 Mar;43(3):870-5. doi: 10.1128/iai.43.3.870-875.1984.

Abstract

A nonpyrogenic desmuramyl peptidolipid, 1-O-(L-alanyl-D-isoglutaminyl-L-alanyl-glycerol-mycolate), had previously been shown to be inactive as adjuvant in guinea pigs, but to be very active in stimulating nonspecific resistance. We now show that 1-O-(L-alanyl-D-isoglutaminyl-L-alanyl-glycerol-mycolate) is capable of enhancing or suppressing the immune responses in mice when injected with or before an antigen. In vivo suppression of the immune response to sheep erythrocytes was also observed with high doses of murabutide, a nonpyrogenic adjuvant-active N-acetylmuramyl-L-alanyl-D-isoglutamine analog. Chemiluminescence measurements with mouse spleen cells show a very strong activity of 1-O-(L-alanyl-D-isoglutaminyl-L-alanyl-glycerol-mycolate) by far superior to the effect obtained with the corresponding muramyl peptide, N-acetylmuramyl-L-alanyl-D-isoglutaminyl-L-alanyl-glycerol-myco late.

摘要

一种无热原性的去muramyl肽脂,1-O-(L-丙氨酰-D-异谷氨酰胺基-L-丙氨酰-甘油-霉菌酸酯),此前已证明在豚鼠中作为佐剂无活性,但在刺激非特异性抵抗力方面非常活跃。我们现在表明,1-O-(L-丙氨酰-D-异谷氨酰胺基-L-丙氨酰-甘油-霉菌酸酯)在与抗原同时注射或在抗原之前注射时,能够增强或抑制小鼠的免疫反应。高剂量的murabutide(一种无热原性的具有佐剂活性的N-乙酰muramyl-L-丙氨酰-D-异谷氨酰胺类似物)在体内也观察到对绵羊红细胞免疫反应的抑制作用。用小鼠脾细胞进行的化学发光测量显示,1-O-(L-丙氨酰-D-异谷氨酰胺基-L-丙氨酰-甘油-霉菌酸酯)具有非常强的活性,远远优于相应的muramyl肽N-乙酰muramyl-L-丙氨酰-D-异谷氨酰胺基-L-丙氨酰-甘油-霉菌酸酯所产生的效果。

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