Expanded Analysis of 20 Pneumococcal Serotypes Associated With Radiographically Confirmed Community-acquired Pneumonia in Hospitalized US Adults

Author:

Isturiz Raul1,Grant Lindsay1,Gray Sharon1,Alexander-Parrish Ronika1,Jiang Qin1,Jodar Luis1,Peyrani Paula1,Ford Kimbal D1,Pride Michael W2,Self Wesley H3,Counselman Francis4,Volturo Gregory5,Ostrosky-Zeichner Luis6,Wunderink Richard G7,Sherwin Robert8,Overcash J Scott9,File Thomas10,Ramirez Julio11

Affiliation:

1. Medical Development, Scientific and Clinical Affairs, Pfizer Inc, Collegeville, Pennsylvania, USA

2. Vaccine Research and Development, Pfizer Inc, Pearl River, New York, USA

3. Department of Emergency Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA

4. Department of Emergency Medicine, Eastern Virginia Medical School, Norfolk, Virginia, USA

5. Department of Emergency Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA

6. McGovern Medical School and Memorial Hermann Medical Center, Houston, Texas, USA

7. Department of Medicine, Pulmonary and Critical Care, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA

8. Department of Emergency Medicine, Wayne State University, Detroit, Michigan, USA

9. eStudySite Clinical Research, Chula Vista, California, USA

10. Summa Health, Northeast Ohio Medical University, Akron, Ohio, USA

11. Division of Infectious Diseases, University of Louisville, Louisville, Kentucky, USA

Abstract

Abstract Background Streptococcus pneumoniae is a causative agent of community-acquired pneumonia (CAP). The 13-valent pneumococcal conjugate vaccine (PCV13) has significantly decreased the burden of PCV13-serotype pneumococcal disease; however, disease from nonvaccine serotypes remains substantial. A recent study documented the persistence of PCV13 serotypes among US adults hospitalized with radiographically confirmed CAP. The current analysis used a recently developed urinary antigen detection (UAD) assay (UAD2) to extend these results to additional serotypes included in an investigational PCV20 vaccine. Methods This prospective study enrolled adults aged ≥18 years hospitalized with radiographically confirmed CAP between October 2013 and September 2016. Presence of S pneumoniae was determined by blood and respiratory sample culture, BinaxNOW urine testing, and UAD. In addition to Quellung on cultured isolates when available, serotypes were identified from urine specimens using UAD1 for PCV13 serotypes and UAD2 for 7 PCV20-unique serotypes (8, 10A, 11A, 12F, 15B, 22F, and 33F) and 4 additional serotypes (2, 9N, 17F, and 20). Results Among 12 055 subjects with radiographically confirmed CAP, 1482 were positive for S pneumoniae. PCV13- and PCV20-unique serotypes were associated with 37.7% (n = 559) and 27.0% (n = 400) of cases, respectively; 288 subjects were exclusively diagnosed as positive for S pneumoniae by UAD2. Demographic and clinical disease characteristics were similar between subjects with CAP caused by PCV13 and PCV20-unique serotypes. Conclusions The current analysis using UAD2 identified a sizeable proportion of hospitalized adult CAP associated with PCV20-unique serotypes. PCV20 may therefore address the burden of CAP caused by the additional serotypes present in the vaccine.

Funder

Pfizer

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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