首页> 美国卫生研究院文献>Human Vaccines Immunotherapeutics >Investigation in a murine model of possible mechanisms of enhanced local reactions to post-primary diphtheria-tetanus toxoid boosters in recipients of acellular pertussis-diphtheria-tetanus vaccine
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Investigation in a murine model of possible mechanisms of enhanced local reactions to post-primary diphtheria-tetanus toxoid boosters in recipients of acellular pertussis-diphtheria-tetanus vaccine

机译:在小鼠模型中研究脱细胞百日咳-白喉-破伤风疫苗接种者对原发性白喉-破伤风类毒素加强剂局部反应增强的可能机制

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摘要

In recipients primed with acellular pertussis diphtheria-tetanus combined vaccine (DTaP) an increased incidence of severe local reactions with extensive redness/swelling has been reported for each subsequent dose of diphtheria-tetanus based combination vaccine given as a booster. This has been attributed to residual active pertussis toxin (PT) in the primary vaccine. In this study, we investigated the possible contribution of the A-subunit enzymatic activity and the B-oligomer carbohydrate binding activity of residual PT in DTaP to local reactions in a murine model using Japanese DTaP batches produced before and after the introduction of a test for reversion of pertussis toxoid to toxin. Residual PT activity was correlated with the B-oligomer carbohydrate binding activity. The in vivo mouse footpad swelling model assay indicated that the B-oligomer carbohydrate binding activity and possibly other factors were associated with intensified sensitization to local reaction following diphtheria toxoid booster.
机译:据报道,在以白喉-破伤风-白破伤风联合疫苗(DTaP)免疫的基础上,接种白喉-破伤风-白破伤风-破伤风联合疫苗(DTaP)的患者,随着剂量的增加,白喉-破伤风联合疫苗的严重局部反应伴随泛红/肿胀的发生率增加。这归因于一级疫苗中残留的活性百日咳毒素(PT)。在这项研究中,我们使用引入DPS的测试前后产生的日本DTaP批次,研究了DTaP中残留PT的A亚基酶活性和B寡聚糖结合活性对鼠模型中局部反应的可能贡献。百日咳类毒素恢复为毒素。残余PT活性与B-低聚物碳水化合物结合活性相关。体内小鼠足垫肿胀模型测定表明,白喉类毒素加强后,B-低聚物的碳水化合物结合活性和可能的​​其他因素与对局部反应的敏化作用增强有关。

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