Meyer-Rienecker H, Jenessen H L, Köhler H, Günther J K
J Neurol. 1976 Feb 13;211(3):229-40.
With the MEM test (Field) one can establish a cellular immune reaction becarus the sensitized lymphocytes release the macrophage slowing factor (MSF) upon interaction with the appropriate antigen. A macrophage migration inhibition was detected in some neurological diseases with destruction of the parenchyma. The modification MEM-LAD (linoleic acid depression) test made further differentiation possible in the 146 neurological patients and normals. The reduction of macrophage mobility inhibition was 94.7 + 4.7% in multiple sclerosis (MS) cases as compared with that of normals of 55.1 + 3.7% and of other neurological diseases of 47.8 + 7.1%. There were no significant differences due to the course and duration of the disease or to immunosuppressive therapy. The pathogenically important results in relatives of MS patients with values between the MS and normal group (78.5 + 0.7%) in mothers suggested a familial (genetic) disposition. The same value was found in a monozygotic twin of an MS patient. The results in the children studied showed that besides the endogenic metabolic component the aetiopathogenically important exogenic factors can operate early in life. In correlation with the principle of the MEM-LAD test the suppressive action of linoleic acid can result in a further therapeutic concept.
通过MEM试验(菲尔德法)能够建立细胞免疫反应,因为致敏淋巴细胞在与相应抗原相互作用时会释放巨噬细胞移动抑制因子(MSF)。在一些伴有实质破坏的神经疾病中检测到了巨噬细胞移动抑制现象。改良的MEM-LAD(亚油酸抑制)试验使对146例神经疾病患者和正常人的进一步区分成为可能。与正常人的55.1±3.7%以及其他神经疾病的47.8±7.1%相比,多发性硬化症(MS)患者巨噬细胞移动抑制的降低率为94.7±4.7%。疾病的病程和持续时间或免疫抑制治疗均未产生显著差异。MS患者亲属中具有介于MS组和正常组之间的值(母亲为78.5±0.7%),这在致病方面的重要结果提示了一种家族性(遗传)倾向。在一名MS患者的同卵双胞胎中也发现了相同的值。对所研究儿童的结果表明,除了内源性代谢成分外,在病因学上重要的外源性因素在生命早期即可起作用。与MEM-LAD试验的原理相关,亚油酸的抑制作用可产生进一步的治疗理念。