Aggett P J, Harries J T, Harvey B A, Soothill J F
J Pediatr. 1979 Mar;94(3):391-4. doi: 10.1016/s0022-3476(79)80578-8.
Selected immunologic functions were assessed in 14 patients with the Shwachman syndrome. Nine patients were neutropenic and four had low levels of IgA or of IgM. Neutrophil mobility was significantly defective in the group of patients as a whole (in 12 it was below the lower limit of normal) and in their parents. No other consistent abnormality in immunity was found. These results suggest that the defective neutrophil mobility is a feature of Shwachman syndrome which may contribute to the vulnerability of these patients to frequent infections. The defect appears to be a primary genetic one, inherited as an autosomal recessive characteristic consistent with the assumed inheritance of Shwachman syndrome.
对14例施瓦茨曼综合征患者的部分免疫功能进行了评估。9例患者存在中性粒细胞减少,4例患者的IgA或IgM水平较低。总体而言,患者组及其父母的中性粒细胞移动能力均存在显著缺陷(12例患者的该指标低于正常下限)。未发现其他一致的免疫异常情况。这些结果表明,中性粒细胞移动能力缺陷是施瓦茨曼综合征的一个特征,这可能导致这些患者易频繁感染。该缺陷似乎是一种原发性遗传缺陷,以常染色体隐性特征遗传,这与施瓦茨曼综合征的假定遗传方式一致。