Evidence map›Paper›PMID 42890491›Full record

ArticleChina CDC weekly2026

Safety of PCV13 with Different Carrier Proteins (CRM197, TT, and TT/DT) - Jiangsu Province, China, 2022-2024.

Xun Li, Borong Xu, Zhiguo Wang, Hongxiong Guo, Yuanyuan Zhu, Ran Hu, Jing Yu

Abstract read
In one paragraph

Article in China CDC weekly, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Xun LiDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Borong XuDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Zhiguo WangDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Hongxiong GuoDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Yuanyuan ZhuDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Ran HuDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.
Jing YuDepartment of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention (Jiangsu Provincial Academy of Preventive Medicine), Nanjing City, Jiangsu Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: This study aimed to evaluate the safety of three kinds of 13-valent pneumococcal conjugate vaccines (PCV13) with different carrier proteins - cross-reactive material 197 (CRM197), tetanus toxoid (TT), and a novel tetanus toxoid/diphtheria toxoid (TT/DT) dual-carrier - by monitoring adverse events following immunization (AEFI) in Jiangsu Province, China. Methods: The Chinese National Adverse Events Following Immunization Information System and Jiangsu Province Vaccination Integrated Service Management Information System were used. Reporting rates (RR) per 100,000 doses were calculated and stratified. Chi-square tests with Bonferroni correction and disproportionality analyses were performed. Results: A total of 1,734,810 PCV13 doses were administered, with 5,195 AEFI reports (RR=299.46 per 100,000 doses). RR was highest for TT/DT-carrier (399.84 per 100,000 doses) versus CRM197-carrier (286.69 per 100,000 doses) and TT-carrier (286.01 per 100,000 doses). Common adverse reactions accounted for 98.23% (5,103/5,195) of all AEFIs, with fever, local redness, and induration being the most common. Disproportionality analysis revealed positive signals for general reactions. Conclusion: All three PCV13 carrier protein types demonstrated acceptable safety profiles in Jiangsu Province from 2022 to 2024. Despite a higher RR for TT/DT-carrier PCV13 than for the other two PCV13 carrier protein types, most AEFIs were mild and common reactions.

Indexed as

Adverse ReactionCarrier ProteinPneumococcal Polysaccharide Conjugate VaccinePost-Marketing Surveillance

Identifiers

PMID42890491
PMCPMC13673390

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.