Literature DB >> 18577410

A clinical trial examining the effect of increased total CRM(197) carrier protein dose on the antibody response to Haemophilus influenzae type b CRM(197) conjugate vaccine.

Vytautas Usonis1, Vytautas Bakasenas, Stephen Lockhart, Sherryl Baker, William Gruber, France Laudat.   

Abstract

CRM(197) is a carrier protein in certain conjugate vaccines. When multiple conjugate vaccines with the same carrier protein are administered simultaneously, reduced response to vaccines and/or antigens related to the carrier protein may occur. This study examined responses of infants who, in addition to diphtheria toxoid/tetanus toxoid/acellular pertussis vaccine (DTaP) received either diphtheria CRM(197)-based Haemophilus influenzae type b conjugate vaccine (HbOC) or HbOC and a diphtheria CRM(197)-based combination 9-valent pneumococcal conjugate vaccine/meningococcal group C conjugate vaccine. Administration of conjugate vaccines with CRM(197) carrier protein load >50 microg did not reduce response to CRM(197) conjugate vaccines or immunogenicity to immunologically cross-reactive diphtheria toxoid.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18577410     DOI: 10.1016/j.vaccine.2008.05.087

Source DB:  PubMed          Journal:  Vaccine        ISSN: 0264-410X            Impact factor:   3.641


  2 in total

1.  Fluorine-modified sialyl-Tn-CRM197 vaccine elicits a robust immune response.

Authors:  Chengcheng Song; Xiu-Jing Zheng; Haili Guo; Yafei Cao; Fan Zhang; Qin Li; Xin-Shan Ye; Yifa Zhou
Journal:  Glycoconj J       Date:  2019-07-02       Impact factor: 2.916

Review 2.  Factors contributing to the immunogenicity of meningococcal conjugate vaccines.

Authors:  Michael Bröker; Francesco Berti; Paolo Costantino
Journal:  Hum Vaccin Immunother       Date:  2016-03-02       Impact factor: 3.452

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.