Journal
CLINICAL INFECTIOUS DISEASES
Volume 74, Issue 9, Pages 1639-1649Publisher
OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciab645
Keywords
indirect protection; invasive pneumococcal disease; Israel epidemiology; pneumococcal conjugate vaccines
Categories
Funding
- Pfizer [0887X1-4603]
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A ten-year surveillance after the implementation of PCV7/PCV13 showed a significant reduction in invasive pneumococcal disease in children and adults, with stabilization after four years. The main PCV13 serotypes were 3, 19A, and 14, while serotypes 8 and 12F were the predominant nonvaccine serotypes.
Ten-year surveillance post-PCV7/PCV13 implementation showed a steep reduction in invasive pneumococcal disease in children and adults, stabilizing after 4 years. The main PCV13 pneumococcal serotypes were 3, 19A, and 14; serotypes 8 and 12F were the leading nonvaccine serotypes. Background. Following 13-valent pneumococcal conjugate vaccine (PCV13) implementation in infants worldwide, overall and vaccine-type invasive pneumococcal disease (IPD) rates declined in children, with variable indirect impact on adults. Methods. A population-based, prospective, nationwide active surveillance of IPD in Israel, 2004-2019 (for adults >= 18 years, 2009-2019). The 7-valent PCV (PCV7)/PCV13 were implemented in Israel in July 2009/November 2010, respectively, with >90% uptake in children <2 years. The 23-valent pneumococcal polysaccharide vaccine (PPV-23) uptake among those >65 years was similar to 75%. For pre-PCV episodes with missing serotype, extrapolations were applied. Overall, PCV13 serotypes (VT13) and non-VT13 (NVT) incidence rate ratios (IRRs) comparing pre-PCV (2004-2008), early-PCV (2009-2011), and late-PCV13 (2016-2019) periods were calculated for different age groups. Results. Overall, 8614 IPD cases were recorded. IPD rates declined by 67% in children <5 and 5-17 years, comparing late-PCV13 versus pre-PCV periods (IRR [95% CI]: .33 [.27-.40] and .33 [.21-.50], respectively). For adults, comparing late-PCV13 with early-PCV periods, rates significantly declined by 53% in those aged 18-44, while rates did not decline significantly in other age groups. VT13 rates significantly declined in all ages, with decline rates ranging between 94% in children <5 years and 60% in adults >= 85 years. NVT rates significantly increased in <5-, 50-64-, and >= 65-year age groups. In the late-PCV13 period, serotypes 3, 14, and 19A remained the predominant VT13, while serotypes 8 and 12F emerged as predominant NVTs. Conclusions. Continuous monitoring of circulating serotypes in all ages demonstrated direct and indirect PCV effects, which are essential for the development of new vaccination strategies.
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