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20-Valent Pneumococcal Conjugate Vaccine: A Review of Its Use in Adults

肺炎链球菌 医学 肺炎球菌结合疫苗 免疫原性 血清型 肺炎球菌多糖疫苗 肺炎球菌肺炎 肺炎球菌病 肺炎球菌感染 免疫学 结合疫苗 耐受性 肺炎 肺炎球菌疫苗 病毒学 微生物学 免疫系统 不利影响 内科学 抗生素 生物
作者
Matt Shirley
出处
期刊:Drugs [Adis, Springer Healthcare]
卷期号:82 (9): 989-999 被引量:27
标识
DOI:10.1007/s40265-022-01733-z
摘要

Acknowledgements During the peer review process, the manufacturer of PCV20 was also offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit. Declarations Funding The preparation of this review was not supported by any external funding. Authorship and Conflict of interest Matt Shirley is a salaried employee of Adis International Ltd/Springer Nature, and declares no relevant conflicts of interest. All authors contributed to the review and are responsible for the article content. Ethics approval, Consent to participate, Consent to publish, Availability of data and material, Code availability Not applicable. Additional information about this Adis Drug Review can be found here.
Abstract The introduction of multi-valent pneumococcal vaccines around the world, such as the 13-valent pneumococcal conjugate vaccine (PCV13), has had a significant effect in reducing the burden of disease caused by Streptococcus pneumoniae infection globally. However, S. pneumoniae serotypes not covered by PCV13 still cause significant disease. A 20-valent pneumococcal conjugate vaccine (PCV20; Prevnar20®; Apexxnar®) has recently been licensed for active immunisation for the prevention of invasive disease and pneumonia caused by S. pneumoniae in adults. PCV20 contains all components of PCV13 with the addition of polysaccharide conjugates of seven more serotypes, selected based on their generalised geographic distribution and relative prevalence as a cause of pneumococcal disease. The immunogenicity of PCV20 in adults has been demonstrated in a well-designed program of clinical trials which showed that PCV20 administered as a single dose by intramuscular injection induced robust immune responses to all 20 S. pneumoniae serotypes covered by the vaccine. PCV20 was well tolerated, with a tolerability and safety profile similar to that for PCV13. By expanding the coverage of disease-causing S. pneumoniae serotypes relative to other PCVs, PCV20 presents a valuable new tool with the potential to further reduce the impact of pneumococcal disease. © Springer Nature Switzerland AG 2022
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