Goldman A S, Goldblum R M
Pediatr Clin North Am. 1977 May;24(2):277-91. doi: 10.1016/s0031-3955(16)33419-8.
Patients with primary disorders of B lymphocytes and immunoglobulins usually display increased susceptibility to bacterial infections but atopic, autoimmune, and malignant disorders are also more common in these patients. The spectrum of these disorders ranges from a virtual absence of B cells and immunoglobulins to selective deficiencies of immunoglobulin subclasses. The diagnosis is dependent upon the demonstration of the immunologic deficits by specialized laboratory procedures which include the quantitation of immunoglobulins, the formation of antibodies in vivo and in vitro and the demonstration of B cells in the tissues or the peripheral blood. There are five major points in the management of these patients: (1) the delineation of the immunologic defects by laboratory testing, (2) the use of parenterally injected human immunoglobulins, (3) the rapid identification of infecting organisms and the prompt institution of appropriate antibiotic therapy, (4) screening the family for immunodeficiency in those cases which are of genetic origin, and (5) genetic counseling.
原发性B淋巴细胞和免疫球蛋白紊乱的患者通常对细菌感染的易感性增加,但这些患者中特应性、自身免疫性和恶性疾病也更常见。这些疾病的范围从几乎没有B细胞和免疫球蛋白到免疫球蛋白亚类的选择性缺陷。诊断依赖于通过专门的实验室程序来证明免疫缺陷,这些程序包括免疫球蛋白的定量、体内和体外抗体的形成以及组织或外周血中B细胞的证明。这些患者的管理有五个要点:(1)通过实验室检测来确定免疫缺陷;(2)使用经肠胃外注射的人免疫球蛋白;(3)快速识别感染生物并及时开始适当的抗生素治疗;(4)在那些有遗传起源的病例中对家族进行免疫缺陷筛查;(5)遗传咨询。