TY - JOUR
T1 - Effect on nasopharyngeal pneumococcal carriage of replacing PCV7 with PCV13 in the Expanded Programme of Immunization in The Gambia
AU - Roca, Anna
AU - Bojang, Abdoulie
AU - Bottomley, Christian
AU - Gladstone, Rebecca A.
AU - Adetifa, Jane U.
AU - Egere, Uzochukwu
AU - Burr, Sarah
AU - Antonio, Martin
AU - Bentley, Stephen
AU - Kampmann, Beate
AU - Oluwalana, Claire
AU - Idoko, Olubukola
AU - Cox, Isatou
AU - Kwambana, Brenda
AU - Jarju, Sheikh
AU - Foster-Nyarko, Ebenezer
AU - Greenwood, Brian
PY - 2015/12/16
Y1 - 2015/12/16
N2 - Introduction: In 2011, two years after the introduction of 7-valent Pneumococcal conjugate vaccine (PCV7), the Gambian immunization programme replaced PVC7 with PCV13 (13-valent). Our objective was to assess the additional impact of PCV13 on prevalence of pneumococcal nasopharyngeal carriage. Methods: We recruited healthy Gambian infants who had received three PCV doses. Nasopharyngeal swabs were collected from infants and their mothers during two cross-sectional surveys (CSS) conducted in infants vaccinated with PCV7 (CSS1) and vaccinated with PCV13 (CSS2). Pneumococci were isolated and serotyped following standardized methods. Whole genome sequencing was performed on non-typable pneumococcus isolated in CSS1 and CSS2. Results: 339 and 350 infants and their mothers were recruited in CSS1 and CSS2, respectively. Overall prevalence of pneumococcal carriage was 85.4% in infants. Among infants, prevalence of vaccine type (VT) carriage was lower in CSS2 [9.4% versus 4.9% (p= 0.025) for PCV7-VT; 33.3% versus 18.3% (p< 0.001) for PCV13-VT and 23.9% versus 13.7% (p= 0.001) for the 6 additional serotypes included in PCV13]. At CSS2, there was a decrease of serotypes 6A (from 15.3% to 5.7%, p< 0.001) and 19F (from 5.6% to 1.7%, p= 0.007), and an increase of non-typable pneumococci (0.3-6.0%, p< 0.001), most of which (82.4%) were from typable serotype backgrounds that had lost the ability to express a capsule. Prevalence of overall and VT carriage in mothers was similar in CSS1 and CSS2. Conclusions: Replacing PCV7 for PCV13 rapidly decreased prevalence of VT carriage among vaccinated Gambian infants. An indirect effect in mothers was not observed yet. Vaccine-driven selection pressure may have been responsible for the increase of non-typable isolates.
AB - Introduction: In 2011, two years after the introduction of 7-valent Pneumococcal conjugate vaccine (PCV7), the Gambian immunization programme replaced PVC7 with PCV13 (13-valent). Our objective was to assess the additional impact of PCV13 on prevalence of pneumococcal nasopharyngeal carriage. Methods: We recruited healthy Gambian infants who had received three PCV doses. Nasopharyngeal swabs were collected from infants and their mothers during two cross-sectional surveys (CSS) conducted in infants vaccinated with PCV7 (CSS1) and vaccinated with PCV13 (CSS2). Pneumococci were isolated and serotyped following standardized methods. Whole genome sequencing was performed on non-typable pneumococcus isolated in CSS1 and CSS2. Results: 339 and 350 infants and their mothers were recruited in CSS1 and CSS2, respectively. Overall prevalence of pneumococcal carriage was 85.4% in infants. Among infants, prevalence of vaccine type (VT) carriage was lower in CSS2 [9.4% versus 4.9% (p= 0.025) for PCV7-VT; 33.3% versus 18.3% (p< 0.001) for PCV13-VT and 23.9% versus 13.7% (p= 0.001) for the 6 additional serotypes included in PCV13]. At CSS2, there was a decrease of serotypes 6A (from 15.3% to 5.7%, p< 0.001) and 19F (from 5.6% to 1.7%, p= 0.007), and an increase of non-typable pneumococci (0.3-6.0%, p< 0.001), most of which (82.4%) were from typable serotype backgrounds that had lost the ability to express a capsule. Prevalence of overall and VT carriage in mothers was similar in CSS1 and CSS2. Conclusions: Replacing PCV7 for PCV13 rapidly decreased prevalence of VT carriage among vaccinated Gambian infants. An indirect effect in mothers was not observed yet. Vaccine-driven selection pressure may have been responsible for the increase of non-typable isolates.
KW - Africa
KW - Epidemiology
KW - Expanded Programme of Immunization
KW - Non-typable
KW - PCV13
KW - PCV7
KW - Vaccine-type
U2 - 10.1016/j.vaccine.2015.11.012
DO - 10.1016/j.vaccine.2015.11.012
M3 - Article
SN - 0264-410X
VL - 33
SP - 7144
EP - 7151
JO - Vaccine
JF - Vaccine
IS - 51
ER -