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Clustering of cases of insulin dependent diabetes (IDDM) occurring three years after hemophilus influenza B (HiB) immunization support causal relationship between immunization and IDDM.

机译:乙型血友病流感(HiB)免疫后三年发生的胰岛素依赖型糖尿病(IDDM)病例的聚类支持了免疫与IDDM之间的因果关系。

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OBJECTIVE: The hemophilus vaccine has been linked to the development of autoimmune type 1 diabetes, insulin dependent diabetes (IDDM) in ecological studies. METHODS: We attempted to determine if the Hemophilus influenza B (HiB) vaccine was associated with an increased risk of IDDM by looking for clusters of cases of IDDM using data from a large clinical trial. All children born in Finland between October 1st, 1985 and August 31st, 1987, approximately 116,000 were randomized to receive 4 doses of the HiB vaccine (PPR-D, Connaught) starting at 3 months of life or one dose starting after 24 months of life. A control-cohort included all 128,500 children born in Finland in the 24 months prior to the HiB vaccine study. Non-obese diabetic prone (NOD) mice were immunized with a hemophilus vaccine to determine if immunization increased the risk of IDDM. RESULTS: The difference in cumulative incidence between those receiving 4 doses and those receiving 0 doses is 54 cases of IDDM/100,000 (P = 0.026) at 7 years, (relative risk = 1.26). Most of the extra cases of IDDM appeared in statistically significant clusters that occurred in periods starting approximately 38 months after immunization and lasting approximately 6-8 months. Immunization with pediatric vaccines increased the risk of insulin diabetes in NOD mice. CONCLUSION: Exposure to HiB immunization is associated with an increased risk of IDDM. NOD mice can be used as an animal model of vaccine induced diabetes.
机译:目的:在生态学研究中,已将血友病疫苗与自身免疫性1型糖尿病,胰岛素依赖型糖尿病(IDDM)的发展联系起来。方法:我们试图通过使用来自大型临床试验的数据寻找IDDM病例群,来确定B型流感嗜血杆菌疫苗是否与IDDM风险增加相关。在1985年10月1日至1987年8月31日期间在芬兰出生的所有儿童中,大约116,000被随机分配,从出生3个月开始接受4剂HiB疫苗(PPR-D,Connaught),或从出生24个月后开始接受一剂。对照组包括HiB疫苗研究前24个月在芬兰出生的所有128,500名儿童。用血友病疫苗免疫非肥胖型糖尿病易感性(NOD)小鼠,以确定免疫是否增加了IDDM的风险。结果:接受4剂和接受0剂的患者在7年时的累积发生率差异为54例IDDM / 100,000(P = 0.026)(相对风险= 1.26)。 IDDM的大多数额外病例均出现在具有统计学意义的簇中,这些簇发生在免疫后约38个月开始,持续约6-8个月。儿科疫苗免疫增加了NOD小鼠发生胰岛素糖尿病的风险。结论:HiB免疫暴露与IDDM风险增加有关。 NOD小鼠可用作疫苗诱导的糖尿病的动物模型。

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