Safety and Immunogenicity of an mRNA-Based hMPV/PIV3 Combination Vaccine in Seropositive Children

被引:2
|
作者
Ghamloush, Sabine Schnyder [1 ]
Essink, Brandon [2 ]
Hu, Bo [1 ]
Kalidindi, Shiva [1 ]
Morsy, Louie [1 ]
Egwuenu-Dumbuya, Chioma [1 ]
Kapoor, Archana [1 ]
Girard, Bethany [1 ]
Dhar, Rakesh [1 ]
Lackey, Rebecca [1 ]
Snape, Matthew D. [3 ]
Shaw, Christine A. [1 ]
机构
[1] Moderna Inc, 200 Technol Sq, Cambridge, MA 02139 USA
[2] MeridiTable San Clin Res, Savannah, GA USA
[3] Moderna Biotech UK Distributor Ltd, London, England
关键词
PARAINFLUENZA VIRUS; HUMAN METAPNEUMOVIRUS; YOUNG-CHILDREN; GLOBAL BURDEN; UNITED-STATES; INFECTION;
D O I
10.1542/peds.2023-064748
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
OBJECTIVES Human metapneumovirus (hMPV) and parainfluenza virus type 3 (PIV3) are common respiratory illnesses in children. The safety and immunogenicity of an investigational mRNA-based vaccine, mRNA-1653, encoding membrane-anchored fusion proteins of hMPV and PIV3, was evaluated in hMPV/PIV3-seropositive children.METHODS In this phase 1b randomized, observer-blind, placebo-controlled, dose-ranging study, hMPV/PIV3-seropositive children were enrolled sequentially into 2 dose levels of mRNA-1653 administered 2 months apart; children aged 12 to 36 months were randomized (1:1) to receive 10-mu g of mRNA-1653 or placebo and children aged 12 to 59 months were randomized (3:1) to receive 30-mu g of mRNA-1653 or placebo.RESULTS Overall, 27 participants aged 18 to 55 months were randomized; 15 participants received 10-mu g of mRNA-1653 (n = 8) or placebo (n = 7), whereas 12 participants received 30-mu g of mRNA-1653 (n = 9) or placebo (n = 3). mRNA-1653 was well-tolerated at both dose levels. The only reported solicited local adverse reaction was tenderness at injection site; solicited systemic adverse reactions included grade 1 or 2 chills, irritability, loss of appetite, and sleepiness. A single 10-mu g or 30-mu g mRNA-1653 injection increased hMPV and PIV3 neutralizing antibody titers (geometric mean fold-rise ratio over baseline: hMPV-A = 2.9-6.1; hMPV-B = 6.2-13.2; PIV3 = 2.8-3.0) and preF and postF binding antibody concentrations (geometric mean fold-rise ratio: hMPV preF = 5.3-6.1; postF = 4.6-6.5 and PIV3 preF = 13.9-14.2; postF = 11.0-12.1); a second injection did not further increase antibody levels in these seropositive children. Binding antibody responses were generally preF biased.CONCLUSIONS mRNA-1653 was well-tolerated and boosted hMPV and PIV3 antibody levels in seropositive children aged 12 to 59 months, supporting the continued development of mRNA-1653 or its components for the prevention of hMPV and PIV3.
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页数:9
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