Forsell J H, Kateley J R, Yoshizawa T, Pestka J J
Appl Environ Microbiol. 1985 Jun;49(6):1523-6. doi: 10.1128/aem.49.6.1523-1526.1985.
Concentrations of T-2, HT-2, 3'-OH T-2, 3'-OH HT-2, T-2 triol, and T-2 tetraol toxins which inhibited [3H]thymidine uptake in mitogen-stimulated human peripheral lymphocytes by 50% were 1.5, 3.5, 4.0, 50, 150, and 150 ng/ml, respectively. The results suggested that the initial hydrolysis of T-2 toxin and the hydroxylation of T-2 toxin to 3'-OH T-2 toxin did not significantly decrease the immunotoxicity of the parent molecule, whereas further hydrolysis to T-2 triol and T-2 tetraol toxins or hydroxylation to 3'-OH HT-2 toxin decreased in vitro toxicity for human lymphocytes.
T-2、HT-2、3'-羟基T-2、3'-羟基HT-2、T-2三醇和T-2四醇毒素抑制丝裂原刺激的人外周血淋巴细胞摄取[3H]胸苷50%时的浓度分别为1.5、3.5、4.0、50、150和150 ng/ml。结果表明,T-2毒素的初始水解以及T-2毒素羟基化为3'-羟基T-2毒素并没有显著降低母体分子的免疫毒性,而进一步水解为T-2三醇和T-2四醇毒素或羟基化为3'-羟基HT-2毒素则降低了对人淋巴细胞的体外毒性。