A dose ranging study of 2 different formulations of 15-valent pneumococcal conjugate vaccine (PCV15) in healthy infants.


Journal

Human vaccines & immunotherapeutics
ISSN: 2164-554X
Titre abrégé: Hum Vaccin Immunother
Pays: United States
ID NLM: 101572652

Informations de publication

Date de publication:
2019
Historique:
pubmed: 29 1 2019
medline: 27 2 2020
entrez: 29 1 2019
Statut: ppublish

Résumé

Two new formulations of an investigational 15-valent pneumococcal conjugate vaccine (PCV15-A and PCV15-B) were developed using 2 different protein-polysaccharide conjugation processes and evaluated in separate phase I/II studies (NCT02037984 [V114-004] and NCT02531373 [V114-005]) to assess optimal concentrations of pneumococcal polysaccharide (PnPs) and Aluminum Phosphate Adjuvant. Various lots of PCV15-A and PCV15-B containing different concentrations of PnPs and/or adjuvant were compared to PCV13 in young adults and infants. Adults received single dose and infants received 4 doses at 2, 4, 6, and 12-15 months of age. Adverse events (AEs) were collected after each dose. Serotype-specific immunoglobulin G (IgG) concentrations and opsonophagocytic activity (OPA) were measured prior and 30 days postvaccination in adults, at 1 month postdose 3 (PD3), pre-dose4, and postdose 4 (PD4) in infants. Safety profiles were comparable across vaccination groups. At PD3, serotype-specific IgG GMCs were generally lower for either PCV15 formulation than PCV13 for most shared serotypes. PCV15 consistently elicited higher antibody responses to the 2 serotypes unique to the vaccine (22F and 33F) and serotype 3 for which PCV13 was shown to be ineffective. Except for serotypes 6A and 6B, no dose-response effect was observed with increasing concentrations of PnPs and/or adjuvant. PCV15 is safe and induces IgG and OPA responses to all 15 serotypes in the vaccine. No significant differences in antibody responses were observed with increases in PnPs and/or Aluminum Phosphate Adjuvant.

Sections du résumé

BACKGROUND
Two new formulations of an investigational 15-valent pneumococcal conjugate vaccine (PCV15-A and PCV15-B) were developed using 2 different protein-polysaccharide conjugation processes and evaluated in separate phase I/II studies (NCT02037984 [V114-004] and NCT02531373 [V114-005]) to assess optimal concentrations of pneumococcal polysaccharide (PnPs) and Aluminum Phosphate Adjuvant.
METHODS
Various lots of PCV15-A and PCV15-B containing different concentrations of PnPs and/or adjuvant were compared to PCV13 in young adults and infants. Adults received single dose and infants received 4 doses at 2, 4, 6, and 12-15 months of age. Adverse events (AEs) were collected after each dose. Serotype-specific immunoglobulin G (IgG) concentrations and opsonophagocytic activity (OPA) were measured prior and 30 days postvaccination in adults, at 1 month postdose 3 (PD3), pre-dose4, and postdose 4 (PD4) in infants.
RESULTS
Safety profiles were comparable across vaccination groups. At PD3, serotype-specific IgG GMCs were generally lower for either PCV15 formulation than PCV13 for most shared serotypes. PCV15 consistently elicited higher antibody responses to the 2 serotypes unique to the vaccine (22F and 33F) and serotype 3 for which PCV13 was shown to be ineffective. Except for serotypes 6A and 6B, no dose-response effect was observed with increasing concentrations of PnPs and/or adjuvant.
CONCLUSION
PCV15 is safe and induces IgG and OPA responses to all 15 serotypes in the vaccine. No significant differences in antibody responses were observed with increases in PnPs and/or Aluminum Phosphate Adjuvant.

Identifiants

pubmed: 30689507
doi: 10.1080/21645515.2019.1568159
pmc: PMC6988874
doi:

Substances chimiques

Antibodies, Bacterial 0
Immunoglobulin G 0
Pneumococcal Vaccines 0
Vaccines, Conjugate 0

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

549-559

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Auteurs

R Rupp (R)

a University of Texas Medical Branch , Galveston , TX , USA.

D Hurley (D)

b Wasatch Pediatrics, Cottonwood Office , Murray , UT , USA.

S Grayson (S)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

J Li (J)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

K Nolan (K)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

R D McFetridge (RD)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

J Hartzel (J)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

C Abeygunawardana (C)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

M Winters (M)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

H Pujar (H)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

P Benner (P)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

L Musey (L)

c Merck & Co., Inc ., Kenilworth , NJ , USA.

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Classifications MeSH