Evidence map›Paper›PMID 28272457›Full record

ArticleScientific reports2017

Novel vaccine potential of Rv3131, a DosR regulon-encoded putative nitroreductase, against hyper-virulent Mycobacterium tuberculosis strain K.

Kee Woong Kwon, Woo Sik Kim, Hongmin Kim, Seung Jung Han, Mi-Young Hahn, Jong Seok Lee, Ki Taek Nam, Sang-Nae Cho, Sung Jae Shin

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. BCGΔBCG1419c increased memory CD8Scientific reports · 2022
    Article
  7. Article
  8. Tuberculosis: The success tale of less explored dormantFrontiers in cellular and infection microbiology · 2022
    Review
  9. Review
  10. Article
  11. Review
  12. GrpE Immunization Protects AgainstFrontiers in immunology · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Frontiers in microbiology · 2017
    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

9 authors.

Kee Woong KwonDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Woo Sik KimDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Hongmin KimDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Seung Jung HanDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Mi-Young HahnDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Jong Seok LeeDepartment of Microbiology Research, International Tuberculosis Research Center, Changwon 51755, South Korea.
Ki Taek NamSeverance Biomedical Science Institute, Brain Korea 21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul 03722, South Korea.
Sang-Nae ChoDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.
Sung Jae ShinDepartment of Microbiology, Yonsei University College of Medicine, Seoul 03722, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence indicates that latency-associated Mycobacterium tuberculosis (Mtb)-specific antigens from the dormancy survival regulator regulon (DosR) may be promising novel vaccine target antigens for the development of an improved tuberculosis vaccine. After transcriptional profiling of DosR-related genes in the hyper-virulent Beijing Mtb strain K and the reference Mtb strain H37Rv, we selected Rv3131, a hypothetical nitroreductase, as a vaccine antigen and evaluated its vaccine efficacy against Mtb K. Mtb K exhibited stable and constitutive up-regulation of rv3131 relative to Mtb H37Rv under three different growth conditions (at least 2-fold induction) including exponential growth in normal culture conditions, hypoxia, and inside macrophages. Mice immunised with Rv3131 formulated in GLA-SE, a well-defined TLR4 adjuvant, displayed enhanced Rv3131-specific IFN-γ and serum IgG2c responses along with effector/memory T cell expansion and remarkable generation of Rv3131-specific multifunctional CD4

Indexed as

Bacterial ProteinsImmunizationNitroreductasesProtein KinasesTuberculosis VaccinesAdjuvants, ImmunologicAnimalsCD4-Positive T-LymphocytesCytokinesDNA-Binding ProteinsFemaleHumansMiceAdjuvants, ImmunologicBacterial ProteinsCytokinesDNA-Binding ProteinsDosR protein, Mycobacterium tuberculosisNitroreductasesProtein KinasesTuberculosis Vaccines

Identifiers

PMID28272457
PMCPMC5341159

What OpenQuestion holds

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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.