Fakunle Y M, Greenwood B M
Lancet. 1976 Sep 18;2(7986):608-9. doi: 10.1016/s0140-6736(76)90671-1.
Serum-IgM is always abnormally high in tropical splenomegaly syndrome. It is postulated that patients with this disease have an abnormal immunoglobulin response to malaria because they lack effective T suppressor cells. This defect may be genetically determined, thus explaining the tribal and familial aggregation of the disease. Hypermacroglobulinaemia is associated with the formation of large amounts of high-molecular-weight immune complexes. These complexes are important in the pathogenesis of the clinical features of the syndrome.
在热带脾肿大综合征中,血清IgM总是异常升高。据推测,该疾病患者对疟疾有异常的免疫球蛋白反应,因为他们缺乏有效的T抑制细胞。这种缺陷可能是由基因决定的,从而解释了该疾病的部落聚集性和家族聚集性。高巨球蛋白血症与大量高分子量免疫复合物的形成有关。这些复合物在该综合征临床特征的发病机制中很重要。