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B族疫苗AlpN在一项安慰剂对照双盲1期试验中的安全性和免疫原性。

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

作者信息

Gonzalez-Miro Majela, Pawlowski Andrzej, Lehtonen Janne, Cao Duojia, Larsson Sara, Darsley Michael, Kitson Geoff, Fischer Per B, Johansson-Lindbom Bengt

机构信息

Immunology Section, Lund University, BMC D14, Lund, Sweden.

Minervax A/S, Ole Maaløes Vej 3, 2200 Copenhagen N, Denmark.

出版信息

iScience. 2023 Feb 21;26(3):106261. doi: 10.1016/j.isci.2023.106261. eCollection 2023 Mar 17.

Abstract

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 αC 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 immunogenicity 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.

摘要

B族链球菌(GBS)是危及新生儿生命的感染及不良妊娠结局亚组的主要病因。基本上所有GBS菌株都拥有α样蛋白(Alp)家族的一个等位基因。一种由AlpαC和Rib的融合N端结构域组成的母体GBS疫苗(GBS-NN),最近在健康成年女性中被证明是安全且具有免疫原性的。为增强对所有临床相关Alp的抗体反应,已开发出第二代疫苗(AlpN),它也包含Alp1的N端结构域以及Alp2和Alp3共有的结构域。在本研究中,通过一项随机、双盲、安慰剂对照、平行组的I期研究评估了AlpN的安全性和免疫原性,该研究纳入了60名健康非妊娠女性。AlpN耐受性良好,能引发针对所有四个Alp-N端结构域同样强烈且持久的抗体反应,从而增强了对疫苗覆盖的所有Alp血清型的调理吞噬杀伤作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b26b/10005905/4f5e51b8024d/fx1.jpg

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