Evidence map›Paper›PMID 39927262›Full record

ArticleFrontiers in microbiology2025

Immunogenicity and protective efficacy of a multi-antigenic adenovirus-based vaccine candidate against

Jin-Seung Yun, Eunkyung Shin, Young-Ran Lee, Jung-Ah Lee, Hyeokjin Lee, Jong-Seok Kim, Sung Jae Shin, Sang-Jun Ha, Sang-Won Lee, Dokeun Kim and 2 more

Erratum issuedAbstract read
In one paragraph

Article in Frontiers in microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Antigen 85B ofVaccines · 2026
    Review
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Jin-Seung YunKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Eunkyung ShinKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Young-Ran LeeBio-Convergence R&D Division, Korea Institute of Ceramic Engineering and Technology, Cheongju, Chungbuk, Republic of Korea.
Jung-Ah LeeKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Hyeokjin LeeKorea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Jong-Seok KimDepartment of Cell Biology, College of Medicine, Myunggok Medical Research Institute, Konyang University, Daejeon, Republic of Korea.
Sung Jae ShinDepartment of Microbiology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sang-Jun HaDepartment of Biochemistry, College of Life Science and Biotechnology, Yonsei University, Seoul, Republic of Korea.
Sang-Won LeeKorea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Dokeun KimKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Jung-Sik YooKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.
Hye-Sook JeongKorea National Institute of Health, Korea Disease Control and Prevention Agency, Cheongju, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The inadequate efficacy of the Bacillus Calmette-Guérin (BCG) vaccine against adult pulmonary tuberculosis (TB) necessitates the development of new and effective vaccines. Human adenovirus serotype 5 (Ad5), which induces T-cell response, is a widely used viral vector. In this study, we aimed to evaluate the efficacy of a multi-antigenic recombinant Ad5 vectored vaccine and determine the optimal immunization route for enhanced immune response against Methods: We constructed a multi-antigenic recombinant Ad5 vectored vaccine expressing four antigens (Ag85B-ESAT6-MPT64-Rv2660c) of Results: Compared with the BCG-only (2 × 10 Conclusion: Our results indicate that rAd-TB4 immunization enhances the immune response to the vaccine boosting antigens in BCG-primed mice, making it a potential adult pulmonary TB vaccine candidate.

Indexed as

adenovirus vectorBCG vaccineimmune responseimmunizationmouse modelmulti-antigenic vaccinepulmonary tuberculosis

Identifiers

PMID39927262
PMCPMC11802578

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.