[Development and application of polysaccharide conjugate vaccine carrier protein].

The development of polysaccharide conjugate vaccines, which convert polysaccharide antigens into T-cell-dependent immunogens through covalent conjugation with protein carriers, represents a critical strategy for enhancing immune protection in infants and young children. Globally licensed conjugate vaccines currently employ carrier proteins including Tetanus Toxoid (TT), Diphtheria Toxoid (DT), and Cross-Reacting Material 197 (CRM197). Recent advances have focused on three key areas: novel carrier protein discovery, optimized conjugation strategies, and evaluation of immune interference during co-administration of multivalent formulations. These efforts aim to achieve broader serotype coverage, prolonged protective efficacy, and simplified immunization schedules. This review synthesizes recent progress in carrier protein development, encompassing vaccine design principles, manufacturing processes, safety profiles, and epidemiological effectiveness. Furthermore, it critically examines current selection criteria for carrier proteins, their clinical applications, and persistent challenges, providing strategic insights to inform future conjugate vaccine development and immunization policy optimization in China.

Authors

Institutions

Publication Details

Journal
PubMed
Published
2025-05-30
DOI
https://doi.org/10.3760/cma.j.cn112150-20250326-00245
Primary Topic
Immunotherapy and Immune Responses
Type
article
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

[Development and application of polysaccharide conjugate vaccine carrier protein].

Y Z Li, J X Li, Xiao Ma, Hongxing Pan et al.
PubMed
Immunotherapy and Immune Responses
article

[Development and application of polysaccharide conjugate vaccine carrier protein].

Y Z Li, J X Li, Xiao Ma, Hongxing Pan, Jun Shao, Ang Lin, Yuting Xu, Zhujun Shao, Bin Hao, A Q Xu
article en

Abstract

The development of polysaccharide conjugate vaccines, which convert polysaccharide antigens into T-cell-dependent immunogens through covalent conjugation with protein carriers, represents a critical strategy for enhancing immune protection in infants and young children. Globally licensed conjugate vaccines currently employ carrier proteins including Tetanus Toxoid (TT), Diphtheria Toxoid (DT), and Cross-Reacting Material 197 (CRM197). Recent advances have focused on three key areas: novel carrier protein discovery, optimized conjugation strategies, and evaluation of immune interference during co-administration of multivalent formulations. These efforts aim to achieve broader serotype coverage, prolonged protective efficacy, and simplified immunization schedules. This review synthesizes recent progress in carrier protein development, encompassing vaccine design principles, manufacturing processes, safety profiles, and epidemiological effectiveness. Furthermore, it critically examines current selection criteria for carrier proteins, their clinical applications, and persistent challenges, providing strategic insights to inform future conjugate vaccine development and immunization policy optimization in China.

PubMedVol. 59
China Pharmaceutical University (CN), Chinese Center For Disease Control and Prevention (CN), Jiangsu Provincial Center for Disease Control and Prevention (CN), Nanjing Municipal Center for Disease Control And Prevention (CN), CanSino (China) (CN), National Institutes for Food and Drug Control (CN), National Institute for Communicable Disease Control and Prevention (CN)
Immunotherapy and Immune Responses
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.