scholarly journals Determining the pneumococcal conjugate vaccine coverage required for indirect protection within Asia and the Pacific: a prospective observational study

2019 ◽  
Vol 7 ◽  
pp. S15
Author(s):  
Jocelyn Chan ◽  
Jana Y Lai ◽  
Claire von Mollendorf ◽  
Christopher Blyth ◽  
David A B Dance ◽  
...  
2020 ◽  
Vol 15 (04) ◽  
pp. 169-175
Author(s):  
Anna Solé-Ribalta ◽  
Maria F. de Sevilla ◽  
Fernando Moraga-Llop ◽  
Alvaro D. Conradi ◽  
Sergi Hernández ◽  
...  

Abstract Objective After the introduction of 13-valent pneumococcal conjugate vaccine (PCV13), a decrease of serotype-3 invasive pneumococcal disease (IPD) has not been homogenously observed around Europe. The aim of the study is to analyze the incidence of serotype-3 IPD in our area (Catalonia, Spain) and describe what microbiological and clinical characteristics distinguish serotype-3 IPD from nonserotype-3 IPD. Methods This study is a prospective observational study performed in three hospitals of Barcelona (Spain), from January 2012 to June 2016. Patients younger than 18 years with a diagnosis of IPD were included. Epidemiological, clinical, and microbiological data were collected. Results A total of 253 cases of IPD were included; of these, 53 were caused by serotype 3. The incidence rate of serotype-3 IPD remained stable over the study years (risk ratio [RR] = 0.64; 95% confidence interval [CI]: 0.3–1.38). In 92.5% (49/53) of the cases of serotype-3 IPD, the diagnosis was pneumonia and 89.8% (44/49) of them reported a complicated pneumonia. Also, 98.1% (52/53) were detected by positive real-time polymerase chain reaction (PCR) in blood or pleural effusion. Seventeen patients were properly vaccinated with PCV13 before the infection. Conclusion After the introduction of PCV13 a global decline of invasive pneumococcal disease has been reported, specially, due to a decrease of serotypes 1 and 19A cases. Serotype-3 Streptococcus pneumoniae IPD remained stable throughout the years of study, being currently the main serotype causing IPD in our area. Serotype 3 causes mostly pneumonia and physicians must be aware of possible complications. Real-time PCR have a significantly higher diagnostic yield for serotype 3 compared with culture. Some vaccination failures were observed.


2013 ◽  
Vol 9 (3) ◽  
pp. 614-620 ◽  
Author(s):  
Filippo Ansaldi ◽  
Daniela de Florentiis ◽  
Paola Canepa ◽  
Antonella Ceravolo ◽  
Emanuela Rappazzo ◽  
...  

JAMA ◽  
2007 ◽  
Vol 297 (16) ◽  
pp. 1784 ◽  
Author(s):  
Rosalyn J. Singleton ◽  
Thomas W. Hennessy ◽  
Lisa R. Bulkow ◽  
Laura L. Hammitt ◽  
Tammy Zulz ◽  
...  

Pneumonia ◽  
2020 ◽  
Vol 12 (1) ◽  
Author(s):  
Sarah Javati ◽  
Geraldine Masiria ◽  
Arthur Elizah ◽  
John-Paul Matlam ◽  
Rebecca Ford ◽  
...  

Abstract Background Maternal immunization with pneumococcal conjugate vaccine (PCV) may protect young infants in high-risk settings against the high risk of pneumococcal infections in early life. The aim of this study was to determine the safety and immunogenicity of 13-valent PCV (PCV13) in healthy women of childbearing age in PNG. Methods As part of this observational study, 50 non-pregnant women of childbearing age (18-45 yrs. old) living in the highlands of PNG were vaccinated with a single dose of PCV13. Local and systemic reactogenicity were assessed 24–48 h after vaccination. Venous blood samples were collected before and 1 month after vaccination to measure PCV13 serotype-specific IgG antibody concentrations. Results No severe adverse effects were reported during the 1-month follow-up period. IgG antibody concentrations significantly increased after vaccination for all PCV13 serotypes. One month after vaccination IgG antibody levels ≥2.5 μg/mL were reached in at least 75% of women for all PCV13 serotypes, except serotype 3, and ≥ 5 μg/mL in at least 75% of women for 7 serotypes (serotypes 6B, 9 V, 14, 18C, 19A, 19F and 23F). Conclusion PCV13 is safe and immunogenic in women of childbearing age living in a high-risk setting in PNG. This supports the implementation of studies to investigate the safety and immunogenicity of maternal PCV vaccination in high-risk settings as a strategy to protect infants in these settings against the high risk of pneumococcal infections in early life. Trial registration NCT04183322. Registered 3 December 2019 - Retrospectively registered


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