Safety and immunogenicity of the group B streptococcus vaccine AlpN in a placebo-controlled double-blind phase 1 trial

被引:6
|
作者
Gonzalez-Miro, Majela [1 ]
Pawlowski, Andrzej [1 ]
Lehtonen, Janne [2 ]
Cao, Duojia [1 ]
Larsson, Sara [1 ]
Darsley, Michael [2 ]
Kitson, Geoff [2 ]
Fischer, Per B. [2 ]
Johansson-Lindbom, Bengt [1 ,2 ]
机构
[1] Lund Univ, Immunol Sect, BMC D14, Lund, Sweden
[2] Minervax AS, Ole Maaloes Vej 3, DK-2200 Copenhagen N, Denmark
基金
欧盟第七框架计划;
关键词
MATERNAL COLONIZATION; C-PROTEIN; DISEASE WORLDWIDE; CONJUGATE VACCINE; TETANUS; HEALTHY; INTERNALIZATION; IMMUNIZATION; DIPHTHERIA; TRANSPORT;
D O I
10.1016/j.isci.2023.106261
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Group B streptococcus (GBS) is a leading cause of life-threatening neonatal infections and subsets of adverse pregnancy outcomes. Essentially all GBS strains possess one allele of the alpha-like protein (Alp) family. A maternal GBS vaccine, consisting of the fused N-terminal domains of the Alps aC and Rib (GBS-NN), was recently demonstrated to be safe and immunogenic in healthy adult women. To enhance antibody responses to all clinically relevant Alps, a second-generation vaccine has been developed (AlpN), also containing the N-terminal domain of Alp1 and the one shared by Alp2 and Alp3. In this study, the safety and immuno-genicity of AlpN is assessed in a randomized, double-blind, placebo-controlled, and parallel-group phase I study, involving 60 healthy non-pregnant women. AlpN is well tolerated and elicits similarly robust and persistent antibody responses against all four Alp-N-terminal domains, resulting in enhanced opsonophagocytic killing of all Alp serotypes covered by the vaccine.
引用
收藏
页数:21
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