Miyawaki Toshio, Kanegane Hirokazu
Department of Pediatrics, Faculty of Medicine, University of Toyama.
Nihon Rinsho. 2010 Jun;68(6):1197-203.
The primary antibody deficiency syndromes are a group of relatively rare disorders characterized by an inability to produce efficient antibody responses, resulting in clinically agammaglobulinemia in affected individuals. Most of them are caused by mutations in genes involved in B cell differentiation. They commonly present with recurrent infections due to encapsulated bacteria. Treatment of primary antibody deficiencies involves immunoglobulin replacement therapy with appropriate antibiotic therapy. However, diagnostic delay in these disorders remains a problem. In this article, we will discuss the pathogenesis, diagnosis, and treatment of primary antibody deficiency syndromes, with some attention to recent advances in this field.
原发性抗体缺陷综合征是一组相对罕见的疾病,其特征是无法产生有效的抗体反应,导致受影响个体临床上出现无丙种球蛋白血症。其中大多数是由参与B细胞分化的基因突变引起的。它们通常因包膜细菌感染而反复出现感染。原发性抗体缺陷的治疗包括免疫球蛋白替代疗法和适当的抗生素治疗。然而,这些疾病的诊断延迟仍然是一个问题。在本文中,我们将讨论原发性抗体缺陷综合征的发病机制、诊断和治疗,并关注该领域的一些最新进展。