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Pneumococcal conjugated vaccine: PHiD-CV.

机译:肺炎球菌结合疫苗:PHiD-CV。

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At the beginning of a new century, we have gained significant achievements against pneumococcal infections by using conjugated pneumococcal vaccines. In January 2009, the EMEA issued a positive opinion about, and recommended the approval of, GlaxoSmithKline's pediatric pneumococcal candidate vaccine, which is indicated for active immunization against invasive pneumococcal disease (IPD) and acute otitis media caused by Streptococcus pneumoniae in infants and children from 6 weeks up to 2 years of age. The approved 10-valent pneumococcal vaccine (PHiD-CV) contains all serotypes in 7-valent pneumococcal conjugate vaccine (PCV-7) plus serotypes 1, 5 and 7F. Protein D from nontypeable Haemophilus influenzae is the carrier protein for eight serotypes, while tetanus and diphtheria toxins are in the carrier proteins for the remaining two serotypes. It has also been proved that PHiD-CV is immunogenic, safe and well-tolerated in children. This vaccine can be coadministered with routinely used pediatric vaccines. Noninferiority criteria of PHiD-CV compared with PCV-7 were established in shared serotypes, except for serotypes 6B and 23F, and PHiD-CV is immunogenic for additional serotypes as assessed by the percentage of subjects with antibody concentrations. PHiD-CV is also immunogenic for ten serotypes as assessed by post-primary and post-booster dose opsonophagocytic activity responses. Vaccine efficacy against IPD and other conditions should be monitored for shared serotypes and also additional serotypes during the postmarketing period. Optimal scheduling, safety and immunogenicity data in children with different risk factors for IPD, or whether it will provide herd immunity, are the questions waiting for answers in the postmarketing period. Further studies are needed to assess the potential advantages of protein D as a carrier and the potential efficacy of this new vaccine against H. influenzae. The potential public health efficacy of PHiD-CV in low-income countries, where IPD and pneumonia are a major public health problem, is a major concern.
机译:在新世纪之初,我们通过使用结合的肺炎球菌疫苗在抗肺炎球菌感染方面取得了重大成就。 2009年1月,欧洲,中东和非洲地区对葛兰素史克的儿科肺炎球菌候选疫苗发表了积极意见,并建议批准该疫苗,该疫苗可针对由婴儿和儿童感染的肺炎链球菌引起的侵袭性肺炎球菌病(IPD)和急性中耳炎进行主动免疫长达2周的年龄为6周。批准的10价肺炎球菌疫苗(PHiD-CV)包含7价肺炎球菌结合疫苗(PCV-7)中的所有血清型,以及血清型1、5和7F。来自不可分型流感嗜血杆菌的蛋白D是八种血清型的载体蛋白,而破伤风和白喉毒素在其余两种血清型的载体蛋白中。还已经证明,PHiD-CV对儿童具有免疫原性,安全性和良好的耐受性。该疫苗可与常规使用的儿科疫苗共同施用。在共享血清型中建立了PHiD-CV与PCV-7相比的非劣效性标准,但血清型6B和23F除外,而PHiD-CV对于其他血清型具有免疫原性,这通过具有抗体浓度的受试者的百分比来评估。 PHiD-CV对十种血清型也具有免疫原性,如通过初次和加强剂量后的调理吞噬细胞活性反应所评估。在上市后期间,应监测针对IPD和其他条件的疫苗有效性,以检测共有的血清型以及其他血清型。在上市后期间,等待具有答案的问题是具有不同IPD危险因素的儿童的最佳日程安排,安全性和免疫原性数据,或者该数据是否具有成群免疫力。需要进一步的研究来评估蛋白质D作为载体的潜在优势以及这种新型疫苗对抗流感嗜血杆菌的潜在功效。在IPD和肺炎是主要的公共卫生问题的低收入国家,PHiD-CV的潜在公共卫生功效引起了人们的极大关注。

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