Antibody Responses to Immunizations in Children with Type I Diabetes Mellitus: a Case-Control Study.

Q2 Biochemistry, Genetics and Molecular Biology
Clinical and Vaccine Immunology Pub Date : 2016-11-04 Print Date: 2016-11-01 DOI:10.1128/CVI.00400-16
Michael Eisenhut, Alexander Chesover, Ronald Misquith, Nisha Nathwani, Andrew Walters
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引用次数: 10

Abstract

Type I diabetes mellitus (DM) has been associated with abnormalities of T cells. Our objective was to assess whether antibody responses to T-cell-dependent and -independent antigens in children with DM are lower than those of children without DM. We performed a case-control study matching children with DM to children without DM by age and by assessing antibody levels to pneumococcal serotypes, Haemophilus influenzae, and tetanus and diphtheria toxoids and reassessing antibody levels in patients with antibody levels below protective thresholds after booster immunization. We recruited 36 children with DM and 36 age-matched controls. The mean age was 10 years. There was no difference between groups in antibody levels against the antigens tested. Pneumococcal antibody levels below the protective threshold were found in 35.9% of DM patients after conjugate pneumococcal vaccination with no difference between groups. Booster immunization with unconjugated pneumococcal vaccine resulted in a median level against pneumococcal serotypes of 2.3 μg/ml (range, 0.05 to 664.7 μg/ml) in children with DM and 6.1 μg/ml (0.12 to 203.36 μg/ml) in children without DM (P = 0.013). Over 85% of children had levels above the protective threshold after booster immunization with no difference between groups. There was no evidence for a reduced antibody response to T-cell-dependent antigens given during childhood immunizations in children with DM. There was a reduced antibody response to antigens of pneumococcal strains in children with DM given unconjugated pneumococcal polysaccharide vaccine compared to that of children without DM without being associated with a difference in percentage of antibody levels below the protective threshold between groups.

1型糖尿病儿童对免疫的抗体反应:一项病例-对照研究
1型糖尿病(DM)与T细胞异常有关。我们的目的是评估糖尿病儿童对t细胞依赖性和非依赖性抗原的抗体反应是否低于非糖尿病儿童。我们进行了一项病例对照研究,将糖尿病儿童与非糖尿病儿童按年龄进行匹配,评估肺炎球菌血清型、流感嗜血杆菌、破伤风和白喉类毒素的抗体水平,并重新评估加强免疫后抗体水平低于保护阈值的患者的抗体水平。我们招募了36名糖尿病儿童和36名年龄匹配的对照组。平均年龄为10岁。两组之间针对抗原的抗体水平没有差异。合并肺炎球菌疫苗接种后,35.9%的糖尿病患者肺炎球菌抗体水平低于保护阈值,组间无差异。非结合肺炎球菌疫苗加强免疫,DM患儿对肺炎球菌血清型的中位水平为2.3 μg/ml(范围为0.05 ~ 664.7 μg/ml),非DM患儿为6.1 μg/ml (0.12 ~ 203.36 μg/ml) (P = 0.013)。在加强免疫后,超过85%的儿童免疫水平高于保护阈值,组间无差异。没有证据表明糖尿病儿童在儿童期免疫接种时对t细胞依赖性抗原的抗体应答降低。与非糖尿病儿童相比,接种非共轭肺炎球菌多糖疫苗的糖尿病儿童对肺炎球菌抗原的抗体应答降低,但与两组之间抗体水平低于保护阈值的百分比差异无关。
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来源期刊
Clinical and Vaccine Immunology
Clinical and Vaccine Immunology 医学-传染病学
CiteScore
2.88
自引率
0.00%
发文量
0
审稿时长
1.5 months
期刊介绍: Cessation. First launched as Clinical and Diagnostic Laboratory Immunology (CDLI) in 1994, CVI published articles that enhanced the understanding of the immune response in health and disease and after vaccination by showcasing discoveries in clinical, laboratory, and vaccine immunology. CVI was committed to advancing all aspects of vaccine research and immunization, including discovery of new vaccine antigens and vaccine design, development and evaluation of vaccines in animal models and in humans, characterization of immune responses and mechanisms of vaccine action, controlled challenge studies to assess vaccine efficacy, study of vaccine vectors, adjuvants, and immunomodulators, immune correlates of protection, and clinical trials.
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