Immunogenicity of Reduced-Dose Monovalent Type 2 Oral Poliovirus Vaccine in Mocuba, Mozambique.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
24 08 2022
Historique:
received: 30 07 2020
accepted: 05 11 2020
pubmed: 13 11 2020
medline: 27 8 2022
entrez: 12 11 2020
Statut: ppublish

Résumé

The monovalent type 2 oral poliovirus vaccine (mOPV2) stockpile is low. One potential strategy to stretch the existing mOPV2 supply is to administer a reduced dose: 1 drop instead of 2. We conducted a randomized, controlled, open-label, noninferiority trial (10% margin) to compared immunogenicity after administration of 1 versus 2 drops of mOPV2. We enrolled 9-22-month-old infants from Mocuba district of Mozambique. Poliovirus neutralizing antibodies were measured in serum samples collected before and 1 month after mOPV2 administration. Immune response was defined as seroconversion from seronegative (<1:8) at baseline to seropositive (≥1:8) after vaccination or boosting titers by ≥4-fold for those with titers between 1:8 and 1:362 at baseline. The trial was registered at anzctr.org.au (no. ACTRN12619000184178p). We enrolled 378 children, and 262 (69%) completed per-protocol requirements. The immune response of mOPV2 was 53.6% (95% confidence interval, 44.9%-62.1%) and 60.6% (52.2%-68.4%) in 1-drop and 2-drop recipients, respectively. The noninferiority margin of the 10% was not reached (difference, 7.0%; 95% confidence interval, -5.0% to 19.0%). A small loss of immunogenicity of reduced mOPV2 was observed. Although the noninferiority target was not achieved, the Strategic Advisory Group of Experts on Immunization recommended the 1-drop strategy as a dose-sparing measure if mOPV2 supplies deteriorate further.

Sections du résumé

BACKGROUND
The monovalent type 2 oral poliovirus vaccine (mOPV2) stockpile is low. One potential strategy to stretch the existing mOPV2 supply is to administer a reduced dose: 1 drop instead of 2.
METHODS
We conducted a randomized, controlled, open-label, noninferiority trial (10% margin) to compared immunogenicity after administration of 1 versus 2 drops of mOPV2. We enrolled 9-22-month-old infants from Mocuba district of Mozambique. Poliovirus neutralizing antibodies were measured in serum samples collected before and 1 month after mOPV2 administration. Immune response was defined as seroconversion from seronegative (<1:8) at baseline to seropositive (≥1:8) after vaccination or boosting titers by ≥4-fold for those with titers between 1:8 and 1:362 at baseline. The trial was registered at anzctr.org.au (no. ACTRN12619000184178p).
RESULTS
We enrolled 378 children, and 262 (69%) completed per-protocol requirements. The immune response of mOPV2 was 53.6% (95% confidence interval, 44.9%-62.1%) and 60.6% (52.2%-68.4%) in 1-drop and 2-drop recipients, respectively. The noninferiority margin of the 10% was not reached (difference, 7.0%; 95% confidence interval, -5.0% to 19.0%).
CONCLUSION
A small loss of immunogenicity of reduced mOPV2 was observed. Although the noninferiority target was not achieved, the Strategic Advisory Group of Experts on Immunization recommended the 1-drop strategy as a dose-sparing measure if mOPV2 supplies deteriorate further.

Identifiants

pubmed: 33180924
pii: 5979486
doi: 10.1093/infdis/jiaa704
pmc: PMC9400415
doi:

Substances chimiques

Antibodies, Viral 0
Poliovirus Vaccine, Inactivated 0
Poliovirus Vaccine, Oral 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

292-298

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America.

Références

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pubmed: 32193361
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pubmed: 29477307
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pubmed: 25316865
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J Infect Dis. 2014 Nov 1;210 Suppl 1:S380-9
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Auteurs

Nilsa de Deus (N)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

Igor Paulo Ubisse Capitine (IPU)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

Adilson Fernando Loforte Bauhofer (AFL)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.
Instituto de Higiene e Medicina Tropical-Universidade Nova de Lisboa, Lisboa, Portugal.

Selma Marques (S)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

Marta Cassocera (M)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.
Instituto de Higiene e Medicina Tropical-Universidade Nova de Lisboa, Lisboa, Portugal.

Assucênio Chissaque (A)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.
Instituto de Higiene e Medicina Tropical-Universidade Nova de Lisboa, Lisboa, Portugal.

Diocreciano Matias Bero (DM)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

José Paulo Langa (JP)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

Fernando Manuel Padama (FM)

Direcção Provincial de Saúde da Zambézia, Mozambique.

Visalakshi Jeyaseelan (V)

Polio Eradication Department, World Health Organization, Geneva, Switzerland.

M Steven Oberste (MS)

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Concepcion F Estivariz (CF)

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

Harish Verma (H)

Polio Eradication Department, World Health Organization, Geneva, Switzerland.

Ilesh Jani (I)

Instituto Nacional de Saúde (INS), Maputo, Mozambique.

Ondrej Mach (O)

Polio Eradication Department, World Health Organization, Geneva, Switzerland.

Roland W Sutter (RW)

Polio Eradication Department, World Health Organization, Geneva, Switzerland.

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Classifications MeSH