Asahi M, Ueda S, Kurakazu M, Urabe H
J Invest Dermatol. 1982 Jan;78(1):38-43. doi: 10.1111/1523-1747.ep12497882.
A highly purified peptide antigen was produced from the cultured mycelia of Trichophyton mentagrophytes. Mycelia were extracted with 0.1 N-HCl at 37 degrees C repeatedly. The protein fraction was precipitated with picric acid and the final product was tentatively designated as Trichophyton mentagrophytes peptide (TMP). Total yield of TMP was about 3% of the original mycelia. When skin tests were done on sensitized guinea pigs, TMP showed a delayed-type reaction. The minimal dose which gave a positive reaction was 3 micrograms (0.1 ml of 30 micrograms/ml solution). Chemical analyses showed that TMP was almost exclusively of a peptide nature and digestion with bacterial peptidase (pronase) completely destroyed its skin test activity, thereby suggesting that protein fraction carried the entire antigenic activity. With chemical and/or physical processings, TMP showed firm stability; the skin test activity was unchanged after heating to 120 degrees C or after processing with HCl or NaOH. Fractionation of TMP by gel filtration demonstrated a considerable heterogeneity in its molecular size, while the antigenic activity was virtually the same in all the fractions. Disc electrophoresis also showed a wide-spread heterogeneous pattern. In the MIF test using peritoneal exudate cells from sensitized guinea pigs, 100 micrograms/ml of TMP had definite inhibitory effect on cell migration.
从须癣毛癣菌培养的菌丝体中制备出一种高度纯化的肽抗原。菌丝体在37℃下用0.1N - HCl反复提取。蛋白质部分用苦味酸沉淀,最终产物暂定为须癣毛癣菌肽(TMP)。TMP的总产量约为原始菌丝体的3%。当对致敏豚鼠进行皮肤试验时,TMP呈现迟发型反应。产生阳性反应的最小剂量为3微克(0.1毫升30微克/毫升的溶液)。化学分析表明,TMP几乎完全是肽性质的,用细菌肽酶(链霉蛋白酶)消化会完全破坏其皮肤试验活性,从而表明蛋白质部分具有全部抗原活性。经过化学和/或物理处理后,TMP表现出很强的稳定性;加热到120℃或用HCl或NaOH处理后,皮肤试验活性不变。通过凝胶过滤对TMP进行分级分离显示其分子大小存在相当大的异质性,而所有级分中的抗原活性实际上是相同的。圆盘电泳也显示出广泛的异质模式。在使用致敏豚鼠腹腔渗出细胞的巨噬细胞移动抑制试验中,100微克/毫升的TMP对细胞迁移有明确的抑制作用。