Montelli T C, Iwasso M T, Peraçoli M T, Mota N G
Arq Neuropsiquiatr. 1981 Mar;39(1):1-12. doi: 10.1590/s0004-282x1981000100001.
The immunological status of five children with West syndrome consequent to previous cerebral lesions was investigated. Three children had West syndrome and two were in transition from West to Lennox-Gastaut syndrome. All of them showed cellular immunological deficiencies in the following tests: sensitization to DNCB, intracutaneous reaction to PHA, inhibition of leucocyte migration, blastic transformation of lymphocytes, T and B lymphocytes in peripheric blood and levels of serum immunoglobulins. These immunological deficiencies, of different degrees of severity, were associated to frequent infections in these children. A possible association between the immunological deficiencies and autoimmunity is discussed.
对五名因先前脑部病变而患有韦斯特综合征的儿童的免疫状态进行了调查。三名儿童患有韦斯特综合征,两名儿童正从韦斯特综合征向伦诺克斯-加斯东综合征转变。在以下测试中,他们均表现出细胞免疫缺陷:对二硝基氯苯的致敏性、对PHA的皮内反应、白细胞迁移抑制、淋巴细胞的母细胞转化、外周血中的T和B淋巴细胞以及血清免疫球蛋白水平。这些不同程度严重的免疫缺陷与这些儿童频繁感染有关。讨论了免疫缺陷与自身免疫之间可能的关联。