Ravindran B, Biswas S, Hussain Q Z, Chaudhuri S N
Immunol Lett. 1984;7(6):329-33. doi: 10.1016/0165-2478(84)90090-7.
Conventional indirect haemagglutination test was performed in rhesus monkey sera (collected from Plasmodium knowlesi infected animals) with and without prior treatment of sera with 2-mercapto-ethanol (2-ME). Surprisingly, many sera samples showed significant enhancement of final titre with 2-ME. The 2-ME enhancement effect was more pronounced in the sera of hyperimmune monkeys on further injection of antigen or parasites. It was also noticeable in the sera during primary drug-suppressed P. knowlesi infection and appeared to have a bearing on the immune status of the animals to rechallenge. The use of a soluble antigen prepared from P. knowlesi infected erythrocytes was found to be essential in IHA test to demonstrate the 2-ME enhancement effect. Antigen prepared from freed parasites (commonly used) failed to show a similar effect in IHA. The possible role of certain T-lymphocyte products - antigen binding, non-agglutinating, 2-ME sensitive molecules - in malarial immunology has been proposed.
对恒河猴血清(采自感染诺氏疟原虫的动物)进行常规间接血凝试验,血清分别经过和未经过2-巯基乙醇(2-ME)处理。令人惊讶的是,许多血清样本经2-ME处理后最终滴度显著提高。在再次注射抗原或寄生虫的情况下,2-ME增强效应在超免疫猴的血清中更为明显。在初次药物抑制的诺氏疟原虫感染期间,血清中也可观察到这种效应,且似乎与动物再次感染的免疫状态有关。发现使用由感染诺氏疟原虫的红细胞制备的可溶性抗原对于在间接血凝试验中证明2-ME增强效应至关重要。由游离寄生虫制备的抗原(常用)在间接血凝试验中未显示出类似效应。有人提出某些T淋巴细胞产物——抗原结合、不凝集、对2-ME敏感的分子——在疟疾免疫学中的可能作用。