Evidence map›Paper›PMID 25589549›Full record

ReviewClinical and vaccine immunology : CVI2015

Quest for correlates of protection against tuberculosis.

Kamlesh Bhatt, Sheetal Verma, Jerrold J Ellner, Padmini Salgame

Open access · diamondAbstract readReview
In one paragraph

Review in Clinical and vaccine immunology : CVI, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 2% 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

87 citing papers in PubMed, 1 synthesis or guideline pooled it, 132 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Antigen 85B ofVaccines · 2026
    Review
  5. Article
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  10. Review
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  13. Review
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  19. The Immunogenicity and Safety ofMicroorganisms · 2023
    Article
  20. Article

27 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 1 country.

Kamlesh BhattDepartment of Medicine, Center for Emerging Pathogens, New Jersey Medical School, Rutgers-The State University of New Jersey, Newark, New Jersey, USA.
Sheetal VermaDepartment of Medicine, Center for Emerging Pathogens, New Jersey Medical School, Rutgers-The State University of New Jersey, Newark, New Jersey, USA.
Jerrold J EllnerSection of Infectious Diseases, Department of Medicine, Boston Medical Center and Boston University School of Medicine, Boston, Massachusetts, USA.
Padmini SalgameDepartment of Medicine, Center for Emerging Pathogens, New Jersey Medical School, Rutgers-The State University of New Jersey, Newark, New Jersey, USA salgampa@njms.rutgers.edu.
Rutgers, The State University of New Jersey · USBoston Medical Center · USRutgers New Jersey Medical School

Funding

Validation and Application of a Model for Human-like TB Latency in RabbitsU19AI111276 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI ALLAND, DAVID, HORSBURGH, CHARLES ROBERT · 2014 to 2020
$23.3M
US-Brazil Research Collaboration on Strain Variation in TBU01AI065663 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI ELLNER, JERROLD J. · 2005 to 2015
$5.2M
NIAID NIH HHS AI065663NIAID NIH HHS AI111276NIAID NIH HHS U01 AI065663NIAID NIH HHS U19 AI111276
6 · The paper itself

Abstract

A major impediment to tuberculosis (TB) vaccine development is the lack of reliable correlates of immune protection or biomarkers that would predict vaccine efficacy. Gamma interferon (IFN-γ) produced by CD4(+) T cells and, recently, multifunctional CD4(+) T cells secreting IFN-γ, tumor necrosis factor (TNF), and interleukin-2 (IL-2) have been used in vaccine studies as a measurable immune parameter, reflecting activity of a vaccine and potentially predicting protection. However, accumulating experimental evidence suggests that host resistance against Mycobacterium tuberculosis infection is independent of IFN-γ and TNF secretion from CD4(+) T cells. Furthermore, the booster vaccine MVA85A, despite generating a high level of multifunctional CD4(+) T cell response in the host, failed to confer enhanced protection in vaccinated subjects. These findings suggest the need for identifying reliable correlates of protection to determine the efficacy of TB vaccine candidates. This article focuses on alternative pathways that mediate M. tuberculosis control and their potential for serving as markers of protection. The review also discusses the significance of investigating the natural human immune response to M. tuberculosis to identify the correlates of protection in vaccination.

Indexed as

BCG VaccineBiomarkersCD4-Positive T-LymphocytesHumansImmunity, InnateImmunologic MemoryInterferon-gammaInterleukin-2Killer Cells, NaturalMycobacterium bovisMycobacterium tuberculosisTh17 CellsTuberculosisTuberculosis VaccinesTumor Necrosis Factor-alphaVaccines, DNABCG VaccineBiomarkersInterferon-gammaInterleukin-2MVA 85ATuberculosis VaccinesTumor Necrosis Factor-alphaVaccines, DNA

Identifiers

PMID25589549
PMCPMC4340894
OpenAlexW2004277637

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.