Dessaint J P, Katz S P, Waksman B H
J Immunopharmacol. 1979;1(3):399-414. doi: 10.3109/08923977909026382.
TAF (T-cell activating factor), produced by peritoneal macrophages and assayed by its ability to potentiate DNA synthesis in macrophage-depleted lymph node cells stimulated with Phytochemagglutinin-concanavalin A, was shown to contain catheptic carboxypeptidase B (CPB) which accounted almost quantitatively for its potentiating activity. TAF action was inhibited by CPB inhibitors and could be mimicked by commercial pig pancreas CPB. The activity was absorbed from active supernatants on EACA-Sepharose and could be eluted with free EACA (epsilon aminocaproic acid).
T细胞激活因子(TAF)由腹膜巨噬细胞产生,通过其增强经植物血凝素-伴刀豆球蛋白A刺激的巨噬细胞耗尽的淋巴结细胞中DNA合成的能力进行测定,结果显示其含有组织蛋白酶羧肽酶B(CPB),该酶几乎定量地解释了其增强活性。TAF的作用被CPB抑制剂抑制,并且可以被商业猪胰腺CPB模拟。该活性从活性上清液中吸附到EACA-琼脂糖上,并且可以用游离的EACA(ε-氨基己酸)洗脱。