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Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam

BACKGROUND: Pneumococcal conjugate vaccines (PCVs) generate herd protection by reducing nasopharyngeal (NP) carriage. Two PCVs, PCV10 and PCV13, have been in use for over a decade, yet there are few data comparing their impact on carriage. Here we report their effect on carriage in a 2+1 schedule, c...

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Autores principales: Temple, Beth, Nation, Monica Larissa, Dai, Vo Thi Trang, Beissbarth, Jemima, Bright, Kathryn, Dunne, Eileen Margaret, Hinds, Jason, Hoan, Pham Thi, Lai, Jana, Nguyen, Cattram Duong, Ortika, Belinda Daniela, Phan, Thanh V., Thuy, Ho Nguyen Loc, Toan, Nguyen Trong, Uyen, Doan Y., Satzke, Catherine, Smith-Vaughan, Heidi, Huu, Tran Ngoc, Mulholland, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052188/
https://www.ncbi.nlm.nih.gov/pubmed/33745731
http://dx.doi.org/10.1016/j.vaccine.2021.02.043
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author Temple, Beth
Nation, Monica Larissa
Dai, Vo Thi Trang
Beissbarth, Jemima
Bright, Kathryn
Dunne, Eileen Margaret
Hinds, Jason
Hoan, Pham Thi
Lai, Jana
Nguyen, Cattram Duong
Ortika, Belinda Daniela
Phan, Thanh V.
Thuy, Ho Nguyen Loc
Toan, Nguyen Trong
Uyen, Doan Y.
Satzke, Catherine
Smith-Vaughan, Heidi
Huu, Tran Ngoc
Mulholland, Kim
author_facet Temple, Beth
Nation, Monica Larissa
Dai, Vo Thi Trang
Beissbarth, Jemima
Bright, Kathryn
Dunne, Eileen Margaret
Hinds, Jason
Hoan, Pham Thi
Lai, Jana
Nguyen, Cattram Duong
Ortika, Belinda Daniela
Phan, Thanh V.
Thuy, Ho Nguyen Loc
Toan, Nguyen Trong
Uyen, Doan Y.
Satzke, Catherine
Smith-Vaughan, Heidi
Huu, Tran Ngoc
Mulholland, Kim
author_sort Temple, Beth
collection PubMed
description BACKGROUND: Pneumococcal conjugate vaccines (PCVs) generate herd protection by reducing nasopharyngeal (NP) carriage. Two PCVs, PCV10 and PCV13, have been in use for over a decade, yet there are few data comparing their impact on carriage. Here we report their effect on carriage in a 2+1 schedule, compared with each other and with unvaccinated controls. METHODS: Data from four groups within a parallel, open-label randomised controlled trial in Ho Chi Minh City contribute to this article. Three groups were randomised to receive a 2+1 schedule of PCV10 (n = 250), a 2+1 schedule of PCV13 (n = 251), or two doses of PCV10 at 18 and 24 months (controls, n = 197). An additional group (n = 199) was recruited at 18 months to serve as controls from 18 to 24 months. NP swabs collected at 2, 6, 9, 12, 18, and 24 months were analysed (blinded) for pneumococcal carriage. This study aimed to determine if PCV10 and PCV13 have a differential effect on pneumococcal carriage, a secondary outcome of the trial. We also describe the serotype distribution among unvaccinated participants. Trial registration: ClinicalTrials.gov NCT01953510. FINDINGS: Compared with unvaccinated controls, a 2+1 schedule of PCV10 reduced PCV10-type carriage by 45–62% from pre-booster through to 24 months of age, and a 2+1 schedule of PCV13 reduced PCV13-type carriage by 36–49% at 12 and 18 months of age. Compared directly with each other, there were few differences between the vaccines in their impact on carriage. Vaccine serotypes accounted for the majority of carriage in unvaccinated participants. INTERPRETATION: Both PCV10 and PCV13 reduce the carriage of pneumococcal vaccine serotypes. The introduction of either vaccine would have the potential to generate significant herd protection in this population. FUNDING: National Health and Medical Research Council of Australia, Bill & Melinda Gates Foundation.
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spelling pubmed-80521882021-04-21 Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam Temple, Beth Nation, Monica Larissa Dai, Vo Thi Trang Beissbarth, Jemima Bright, Kathryn Dunne, Eileen Margaret Hinds, Jason Hoan, Pham Thi Lai, Jana Nguyen, Cattram Duong Ortika, Belinda Daniela Phan, Thanh V. Thuy, Ho Nguyen Loc Toan, Nguyen Trong Uyen, Doan Y. Satzke, Catherine Smith-Vaughan, Heidi Huu, Tran Ngoc Mulholland, Kim Vaccine Article BACKGROUND: Pneumococcal conjugate vaccines (PCVs) generate herd protection by reducing nasopharyngeal (NP) carriage. Two PCVs, PCV10 and PCV13, have been in use for over a decade, yet there are few data comparing their impact on carriage. Here we report their effect on carriage in a 2+1 schedule, compared with each other and with unvaccinated controls. METHODS: Data from four groups within a parallel, open-label randomised controlled trial in Ho Chi Minh City contribute to this article. Three groups were randomised to receive a 2+1 schedule of PCV10 (n = 250), a 2+1 schedule of PCV13 (n = 251), or two doses of PCV10 at 18 and 24 months (controls, n = 197). An additional group (n = 199) was recruited at 18 months to serve as controls from 18 to 24 months. NP swabs collected at 2, 6, 9, 12, 18, and 24 months were analysed (blinded) for pneumococcal carriage. This study aimed to determine if PCV10 and PCV13 have a differential effect on pneumococcal carriage, a secondary outcome of the trial. We also describe the serotype distribution among unvaccinated participants. Trial registration: ClinicalTrials.gov NCT01953510. FINDINGS: Compared with unvaccinated controls, a 2+1 schedule of PCV10 reduced PCV10-type carriage by 45–62% from pre-booster through to 24 months of age, and a 2+1 schedule of PCV13 reduced PCV13-type carriage by 36–49% at 12 and 18 months of age. Compared directly with each other, there were few differences between the vaccines in their impact on carriage. Vaccine serotypes accounted for the majority of carriage in unvaccinated participants. INTERPRETATION: Both PCV10 and PCV13 reduce the carriage of pneumococcal vaccine serotypes. The introduction of either vaccine would have the potential to generate significant herd protection in this population. FUNDING: National Health and Medical Research Council of Australia, Bill & Melinda Gates Foundation. Elsevier Science 2021-04-15 /pmc/articles/PMC8052188/ /pubmed/33745731 http://dx.doi.org/10.1016/j.vaccine.2021.02.043 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Temple, Beth
Nation, Monica Larissa
Dai, Vo Thi Trang
Beissbarth, Jemima
Bright, Kathryn
Dunne, Eileen Margaret
Hinds, Jason
Hoan, Pham Thi
Lai, Jana
Nguyen, Cattram Duong
Ortika, Belinda Daniela
Phan, Thanh V.
Thuy, Ho Nguyen Loc
Toan, Nguyen Trong
Uyen, Doan Y.
Satzke, Catherine
Smith-Vaughan, Heidi
Huu, Tran Ngoc
Mulholland, Kim
Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title_full Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title_fullStr Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title_full_unstemmed Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title_short Effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: Results from a randomised controlled trial in Vietnam
title_sort effect of a 2+1 schedule of ten-valent versus 13-valent pneumococcal conjugate vaccine on pneumococcal carriage: results from a randomised controlled trial in vietnam
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8052188/
https://www.ncbi.nlm.nih.gov/pubmed/33745731
http://dx.doi.org/10.1016/j.vaccine.2021.02.043
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