| Literature DB >> 25323223 |
Sarah Browall1, Erik Backhaus2, Pontus Naucler3, Ilias Galanis4, Karin Sjöström4, Diana Karlsson5, Stefan Berg6, Joachim Luthander7, Margareta Eriksson7, Carl Spindler8, Mikael Ejdebäck5, Birger Trollfors6, Jessica Darenberg9, Mats Kalin8, Ake Örtqvist10, Rune Andersson11, Birgitta Henriques-Normark12.
Abstract
Pneumococcal conjugated vaccines (PCVs) have shown protection against invasive pneumococcal disease by vaccine serotypes, but an increase in non-vaccine serotype disease has been observed. Type-specific effects on clinical manifestation need to be explored. Clinical data from 2096 adults and 192 children with invasive pneumococcal disease were correlated to pneumococcal molecular serotypes. Invasive disease potential for pneumococcal serotypes were calculated using 165 invasive and 550 carriage isolates from children. The invasive disease potential was lower for non-PCV13 compared to vaccine-type strains. Patients infected with non-PCV13 strains had more underlying diseases, were less likely to have pneumonia and, in adults, tended to have a higher mortality. Furthermore, patients infected with pneumococci belonging to clonal serotypes only expressing non-PCV13 capsules had a higher risk for septicaemia and mortality. PCV vaccination will probably lead to a decrease in invasive pneumococcal disease but an alteration in the clinical manifestation of invasive pneumococcal disease. Genetic lineages causing invasive pneumococcal disease in adults often express non-vaccine serotypes, which can expand after vaccination with an increased risk of infection in patients with underlying diseases. ©ERS 2014.Entities:
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Year: 2014 PMID: 25323223 DOI: 10.1183/09031936.00080814
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671