Szczawinska-Poplonyk Aleksandra, Breborowicz Anna, Samara Husam, Ossowska Lidia, Dworacki Grzegorz
Department of Pediatric Pneumonology, Allergology and Clinical Immunology, III Chair of Pediatrics, Poznan University of Medical Science, Poznan, Poland
Department of Pediatric Pneumonology, Allergology and Clinical Immunology, III Chair of Pediatrics, Poznan University of Medical Science, Poznan, Poland.
Clin Vaccine Immunol. 2015 Aug;22(8):875-82. doi: 10.1128/CVI.00148-15. Epub 2015 May 27.
The impaired synthesis of antigen-specific antibodies, which is indispensable for an adaptive immune response to infections, is a fundamental pathomechanism that leads to clinical manifestations in children with antibody production defects. The aim of this study was to evaluate the synthesis of antigen-specific antibodies following immunization in relation to peripheral blood B cell subsets in young children with hypogammaglobulinemia. Twenty-two children, aged from 8 to 61 months, with a deficiency in one or more major immunoglobulin classes participated in the study. Postvaccination antibodies against tetanus and diphtheria toxoids, the surface antigen of the hepatitis B virus, and the capsular Haemophilus influenzae type b polysaccharide antigen were assessed along with an immunophenotypic evaluation of peripheral blood B lymph cell maturation. A deficiency of antibodies against the tetanus toxoid was assessed in 73% of cases and that against the diphtheria toxoid was assessed in 68% of cases, whereas a deficiency of antibodies against the surface antigen of the hepatitis B virus was revealed in 59% of the children included in the study. A defective response to immunization with a conjugate vaccine with the Haemophilus influenzae type b polysaccharide antigen was demonstrated in 55% of hypogammaglobulinemic patients. Increased proportions of transitional B lymph cells and an accumulation of plasmablasts accompanied antibody deficiencies. The defective response to vaccine protein and polysaccharide antigens is a predominating disorder of humoral immunity in children with hypogammaglobulinemia and may result from a dysfunctional state of the cellular elements of the immune system.
抗原特异性抗体的合成受损是抗体产生缺陷患儿出现临床表现的一种基本病理机制,而抗原特异性抗体的合成对于感染的适应性免疫反应至关重要。本研究的目的是评估低丙种球蛋白血症幼儿免疫接种后抗原特异性抗体的合成情况及其与外周血B细胞亚群的关系。22名年龄在8至61个月之间、一种或多种主要免疫球蛋白类别缺乏的儿童参与了本研究。对接种疫苗后针对破伤风类毒素、白喉类毒素、乙型肝炎病毒表面抗原和b型流感嗜血杆菌荚膜多糖抗原的抗体进行了评估,并对外周血B淋巴细胞成熟情况进行了免疫表型评估。73%的病例评估出破伤风类毒素抗体缺乏,68%的病例评估出白喉类毒素抗体缺乏,而在纳入研究的儿童中,59%的儿童显示出乙型肝炎病毒表面抗原抗体缺乏。55%的低丙种球蛋白血症患者表现出对含b型流感嗜血杆菌多糖抗原的结合疫苗免疫接种反应缺陷。过渡性B淋巴细胞比例增加和成浆细胞积聚伴随着抗体缺乏。对疫苗蛋白和多糖抗原的反应缺陷是低丙种球蛋白血症患儿体液免疫的主要紊乱,可能是由于免疫系统细胞成分的功能失调状态所致。