Evidence map›Paper›PMID 25905680›Full record

ArticleHuman vaccines & immunotherapeutics2015

Immunogenicity and protective efficacy of DMT liposome-adjuvanted tuberculosis subunit CTT3H vaccine.

Xindong Teng, Maopeng Tian, Jianrong Li, Songwei Tan, Xuefeng Yuan, Qi Yu, Yukai Jing, Zhiping Zhang, Tingting Yue, Lei Zhou and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Research Progress on Liposome Pulmonary Delivery ofJournal of aerosol medicine and pulmonary drug delivery · 2024
    Review
  6. Liposomal delivery system/adjuvant for tuberculosis vaccine.Immunity, inflammation and disease · 2023
    Review
  7. Review
  8. Article
  9. Immunogenicity of heparin-binding hemagglutinin expressed byIranian journal of basic medical sciences · 2018
    Article
  10. Heterologous Boost FollowingFrontiers in immunology · 2018
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. A New Adjuvant MTOM MediatesFrontiers in immunology · 2017
    Article
  16. Article
  17. Article
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

11 authors at 2 institutions in 1 country.

Xindong Tenga Department of Pathogen Biology; School of Basic Medicine; Huazhong University of Science & Technology ; Wuhan , PR China.
Maopeng Tian
Jianrong Li
Songwei Tan
Xuefeng Yuan
Qi Yu
Yukai Jing
Zhiping Zhang
Tingting Yue
Lei Zhou
Xionglin Fan
Huazhong University of Science and Technology · CNBeijing Administration Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Different strategies have been proposed for the development of protein subunit vaccine candidates for tuberculosis (TB), which shows better safety than other types of candidates and the currently used Bacillus Calmette-Guérin (BCG) vaccine. In order to develop more effective protein subunits depending on the mechanism of cell-mediated immunity against TB, a polyprotein CTT3H, based on 5 immunodominant antigens (CFP10, TB10.4, TB8.4, Rv3615c, and HBHA) with CD8(+) epitopes of Mycobacterium tuberculosis, was constructed in this study. We vaccinated C57BL/6 mice with a TB subunit CTT3H protein in an adjuvant of dimethyldioctadecylammonium/monophosphoryl lipid A/trehalose 6,6'-dibehenate (DDA/MPL/TDB, DMT) liposome to investigate the immunogenicity and protective efficacy of this novel vaccine. Our results demonstrated that DMT liposome-adjuvanted CTT3H vaccine not only induced an antigen-specific CD4(+) Th1 response, but also raised the number of PPD- and CTT3H-specific IFN-γ(+) CD8(+) T cells and elicited strong CTL responses against TB10.4, which provided more effective protection against a 60 CFU M. tuberculosis aerosol challenge than PBS control and DMT adjuvant alone. Our findings indicate that DMT-liposome is an effective adjuvant to stimulate CD8(+) T cell responses and the DMT-adjuvanted subunit CTT3H vaccine is a promising candidate for the next generation of TB vaccine.

Indexed as

Adjuvants, ImmunologicAnimalsAntigens, BacterialCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesDisease Models, AnimalFemaleLiposomesMice, Inbred C57BLMycobacterium tuberculosisRecombinant Fusion ProteinsTuberculosisTuberculosis VaccinesVaccines, SubunitVaccines, SyntheticAdjuvants, ImmunologicAntigens, BacterialLiposomesRecombinant Fusion ProteinsTuberculosis VaccinesVaccines, SubunitVaccines, SyntheticadjuvantDDAMPLsubunit vaccineTDBtuberculosis

Identifiers

PMID25905680
PMCPMC4514263
OpenAlexW1510313930

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.