TY - JOUR
T1 - A cross-sectional observational study of pneumococcal carriage in children, their parents, and older adults following the introduction of the 7-valent pneumococcal conjugate vaccine
AU - Hamaluba, Mainga
AU - Kandasamy, Rama
AU - Ndimah, Susan
AU - Morton, Richard
AU - Caccamo, Marisa
AU - Robinson, Hannah
AU - Kelly, Sarah
AU - Field, Aimee
AU - Norman, Lily
AU - Plested, Emma
AU - Thompson, Ben A V
AU - Zafar, Azhar
AU - Kerridge, Simon A
AU - Lazarus, Rajeka
AU - John, Tessa
AU - Holmes, Jane
AU - Fenlon, Shannon N
AU - Gould, Katherine A
AU - Waight, Pauline
AU - Hinds, Jason
AU - Crook, Derrick
AU - Snape, Matthew D
AU - Pollard, Andrew J
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Using nasopharyngeal carriage as a marker of vaccine impact, pneumococcal colonization and its relation to invasive disease were examined in children, their parents, and older adults in the United Kingdom following introduction of 7-valent pneumococcal conjugate vaccine (PCV7) and prior to 13-valent pneumococcal conjugate vaccine (PCV13).A cross-sectional observational study was conducted, collecting nasopharyngeal swabs from children aged 25 to 55 months who had previously received 3 doses of PCV7, their parents, and adults aged ≥65 years. Pneumococcal serotyping was conducted according to World Health Organization guidelines with nontypeable isolates further analyzed by molecular serotyping. A national invasive disease surveillance program was conducted throughout the corresponding period.Pneumococcus was isolated from 47% of children, 9% of parents, and 2.2% of older adults. For these groups, the percentage of serotypes covered by PCV7 were 1.5%, 0.0%, and 15.4%, with a further 20.1%, 44.4%, and 7.7% coverage added by those in PCV13. In each group, the percentage of disease due to serotypes covered by PCV7 were 1.0%, 7.4% and 5.1% with a further 65.3%, 42.1%, and 61.4% attributed to those in PCV13.The prevalence of carriage is the highest in children, with direct vaccine impact exemplified by low carriage and disease prevalence of PCV7 serotypes in vaccinated children, whereas the indirect effects of herd protection are implied by similar observations in unvaccinated parents and older adults.
AB - Using nasopharyngeal carriage as a marker of vaccine impact, pneumococcal colonization and its relation to invasive disease were examined in children, their parents, and older adults in the United Kingdom following introduction of 7-valent pneumococcal conjugate vaccine (PCV7) and prior to 13-valent pneumococcal conjugate vaccine (PCV13).A cross-sectional observational study was conducted, collecting nasopharyngeal swabs from children aged 25 to 55 months who had previously received 3 doses of PCV7, their parents, and adults aged ≥65 years. Pneumococcal serotyping was conducted according to World Health Organization guidelines with nontypeable isolates further analyzed by molecular serotyping. A national invasive disease surveillance program was conducted throughout the corresponding period.Pneumococcus was isolated from 47% of children, 9% of parents, and 2.2% of older adults. For these groups, the percentage of serotypes covered by PCV7 were 1.5%, 0.0%, and 15.4%, with a further 20.1%, 44.4%, and 7.7% coverage added by those in PCV13. In each group, the percentage of disease due to serotypes covered by PCV7 were 1.0%, 7.4% and 5.1% with a further 65.3%, 42.1%, and 61.4% attributed to those in PCV13.The prevalence of carriage is the highest in children, with direct vaccine impact exemplified by low carriage and disease prevalence of PCV7 serotypes in vaccinated children, whereas the indirect effects of herd protection are implied by similar observations in unvaccinated parents and older adults.
KW - Adult
KW - Aged
KW - Child, Preschool
KW - Cross-Sectional Studies
KW - Female
KW - Humans
KW - Male
KW - Nasopharynx/drug effects
KW - Pneumococcal Infections/prevention & control
KW - Serogroup
KW - Streptococcus pneumoniae/genetics
KW - Vaccines, Conjugate/pharmacology
U2 - 10.1097/MD.0000000000000335
DO - 10.1097/MD.0000000000000335
M3 - Article (Academic Journal)
C2 - 25569650
SN - 0025-7974
VL - 94
SP - e335
JO - Medicine (Baltimore)
JF - Medicine (Baltimore)
IS - 1
ER -