7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Safety, Tolerability, and Immunogenicity of a 20-Valent Pneumococcal Conjugate Vaccine (PCV20) in Adults 60 to 64 Years of Age

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Pneumococcal conjugate vaccines (PCVs) have significantly decreased pneumococcal disease worldwide; however, expanding serotype coverage may further reduce disease burden. A 20-valent PCV (PCV20) containing capsular polysaccharide conjugates of serotypes present in the 13-valent PCV (PCV13) and 7 new serotypes (8, 10A, 11A, 12F, 15B, 22F, and 33F) is currently in development. This phase 2 study evaluated safety, tolerability, and immunogenicity of PCV20 in adults without prior pneumococcal vaccination.

          Methods

          In this randomized, active-controlled, double-blinded trial, 444 adults 60 through 64 years of age were randomized to receive either a single dose of PCV20 followed 1 month later by saline placebo or a single dose of PCV13 followed 1 month later by 23-valent polysaccharide vaccine. Local injection site reactions, select systemic symptoms, and adverse events (AEs) were recorded. Immunogenicity was assessed by measuring serotype-specific opsonophagocytic activity (OPA) titers before and approximately 1 month after each vaccination.

          Results

          Local reaction and systemic event rates were similar after vaccination with PCV20 or PCV13; no serious vaccine-related AEs were reported. In the PCV20 group, functional immune responses as measured by OPA were robust for all 20 serotypes included in the vaccine, with geometric mean fold rises from baseline ranging from 6.0 to 113.4.

          Conclusions

          PCV20 was well tolerated in adults 60 to 64 years of age, with a safety profile consistent with historical experience of PCVs in this age group. Substantial OPA responses were elicited against all serotypes. Results demonstrate the potential for PCV20 to expand pneumococcal disease protection.

          Clinical Trials Registration

          NCT03313037.

          Abstract

          A 20-valent pneumococcal conjugate vaccine (PCV20) is being developed to expand serotype coverage beyond the 13-valent PCV (PCV13). In older adults, PCV20 exhibited safety and tolerability consistent with PCV13. PCV20 elicited robust immune responses to all 20 vaccine serotypes.

          Related collections

          Most cited references36

          • Record: found
          • Abstract: found
          • Article: not found

          Sustained reductions in invasive pneumococcal disease in the era of conjugate vaccine.

          Changes in invasive pneumococcal disease (IPD) incidence were evaluated after 7 years of 7-valent pneumococcal conjugate vaccine (PCV7) use in US children. Laboratory-confirmed IPD cases were identified during 1998-2007 by 8 active population-based surveillance sites. We compared overall, age group-specific, syndrome-specific, and serotype group-specific IPD incidence in 2007 with that in 1998-1999 (before PCV7) and assessed potential serotype coverage of new conjugate vaccine formulations. Overall and PCV7-type IPD incidence declined by 45% (from 24.4 to 13.5 cases per 100,000 population) and 94% (from 15.5 to 1.0 cases per 100,000 population), respectively (P< .01 all age groups). The incidence of IPD caused by serotype 19A and other non-PCV7 types increased from 0.8 to 2.7 cases per 100,000 population and from 6.1 to 7.9 cases per 100,000 population, respectively (P< .01 for all age groups). The rates of meningitis and invasive pneumonia caused by non-PCV7 types increased for all age groups (P< .05), whereas the rates of primary bacteremia caused by these serotypes did not change. In 2006-2007, PCV7 types caused 2% of IPD cases, and the 6 additional serotypes included in an investigational 13-valent conjugate vaccine caused 63% of IPD cases among children <5 years-old. Dramatic reductions in IPD after PCV7 introduction in the United States remain evident 7 years later. IPD rates caused by serotype 19A and other non-PCV7 types have increased but remain low relative to decreases in PCV7-type IPD.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Effect of use of 13-valent pneumococcal conjugate vaccine in children on invasive pneumococcal disease in children and adults in the USA: analysis of multisite, population-based surveillance.

            In 2000, seven-valent pneumococcal conjugate vaccine (PCV7) was introduced in the USA and resulted in dramatic reductions in invasive pneumococcal disease (IPD) and moderate increases in non-PCV7 type IPD. In 2010, PCV13 replaced PCV7 in the US immunisation schedule. We aimed to assess the effect of use of PCV13 in children on IPD in children and adults in the USA.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Polysaccharide conjugate vaccine against pneumococcal pneumonia in adults.

              Pneumococcal polysaccharide conjugate vaccines prevent pneumococcal disease in infants, but their efficacy against pneumococcal community-acquired pneumonia in adults 65 years of age or older is unknown.
                Bookmark

                Author and article information

                Journal
                Clin Infect Dis
                Clin Infect Dis
                cid
                Clinical Infectious Diseases: An Official Publication of the Infectious Diseases Society of America
                Oxford University Press (US )
                1058-4838
                1537-6591
                01 October 2021
                27 July 2020
                27 July 2020
                : 73
                : 7
                : e1489-e1497
                Affiliations
                [1 ]Medical Research South , LLC, Charleston, South Carolina, USA
                [2 ]Lynn Health Science Institute , Oklahoma City, Oklahoma, USA
                [3 ]Vaccine Research and Development, Pfizer Inc , Collegeville, Pennsylvania, USA
                [4 ]Vaccine Research and Development, Pfizer Inc , Pearl River, New York, USA
                Author notes
                Correspondence: M. Young Jr, Vaccine Research and Development, Pfizer Inc, 500 Arcola Rd, Collegeville, PA 19426 ( mariano.young-jr@ 123456pfizer.com ).
                Article
                ciaa1045
                10.1093/cid/ciaa1045
                8492133
                32716500
                4cd248dc-45ba-4653-9929-d4ecca74bc05
                © The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence ( https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                : 20 March 2020
                : 24 June 2020
                : 20 July 2020
                : 29 September 2020
                Page count
                Pages: 9
                Funding
                Funded by: Pfizer Inc., DOI 10.13039/100004319;
                Award ID: SAF2016-80033-R
                Categories
                Online Only Articles
                Major Articles and Commentaries
                AcademicSubjects/MED00290

                Infectious disease & Microbiology
                adult,immunogenicity and safety,20-valent pneumococcal conjugate vaccine,streptococcus pneumoniae,clinical trial

                Comments

                Comment on this article