Evidence map›Paper›PMID 19458207›Full record

ArticleClinical and vaccine immunology : CVI2009

Development of a murine mycobacterial growth inhibition assay for evaluating vaccines against Mycobacterium tuberculosis.

Marcela Parra, Amy L Yang, JaeHyun Lim, Kristopher Kolibab, Steven Derrick, Nathalie Cadieux, Liyanage P Perera, William R Jacobs, Michael Brennan, Sheldon L Morris

Open access · diamondAbstract read
In one paragraph

Article in Clinical and vaccine immunology : CVI, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 13% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. TheF1000Research · 2021
    Article
  7. Article
  8. RNA Sensing ofVaccines · 2020
    Review
  9. Article
  10. Article
  11. Article
  12. Frontiers in immunology · 2019
    Article
  13. Vaccine-Mediated Mechanisms Controlling Replication ofFrontiers in cellular and infection microbiology · 2018
    Article
  14. Frontiers in immunology · 2018
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 6 institutions in 1 country.

Marcela ParraCenter for Biologics Evaluation and Research, United States Food and Drug Administration, Bethesda, MD 20892, USA.
Amy L Yang
JaeHyun Lim
Kristopher Kolibab
Steven Derrick
Nathalie Cadieux
Liyanage P Perera
William R Jacobs
Michael Brennan
Sheldon L Morris
Aeras · USAlbert Einstein College of Medicine · USCenter for Biologics Evaluation and Research · USCenter for Cancer Research · USHoward Hughes Medical Institute · USUnited States Food and Drug Administration · US

Funding

PHS HHS IAA 224-06-1322
6 · The paper itself

Abstract

The development and characterization of new tuberculosis (TB) vaccines has been impeded by the lack of reproducible and reliable in vitro assays for measuring vaccine activity. In this study, we developed a murine in vitro mycobacterial growth inhibition assay for evaluating TB vaccines that directly assesses the capacity of immune splenocytes to control the growth of Mycobacterium tuberculosis within infected macrophages. Using this in vitro assay, protective immune responses induced by immunization with five different types of TB vaccine preparations (Mycobacterium bovis BCG, an attenuated M. tuberculosis mutant strain, a DNA vaccine, a modified vaccinia virus strain Ankara [MVA] construct expressing four TB antigens, and a TB fusion protein formulated in adjuvant) can be detected. Importantly, the levels of vaccine-induced mycobacterial growth-inhibitory responses seen in vitro after 1 week of coculture correlated with the protective immune responses detected in vivo at 28 days postchallenge in a mouse model of pulmonary tuberculosis. In addition, similar patterns of cytokine expression were evoked at day 7 of the in vitro culture by immune splenocytes taken from animals immunized with the different TB vaccines. Among the consistently upregulated cytokines detected in the immune cocultures are gamma interferon, growth differentiation factor 15, interleukin-21 (IL-21), IL-27, and tumor necrosis factor alpha. Overall, we have developed an in vitro functional assay that may be useful for screening and comparing new TB vaccine preparations, investigating vaccine-induced protective mechanisms, and assessing manufacturing issues, including product potency and stability.

Indexed as

AnimalsCoculture TechniquesCytokinesLeukocytes, MononuclearMacrophagesMiceMycobacterium tuberculosisTuberculosisTuberculosis VaccinesCytokinesTuberculosis Vaccines

Identifiers

PMID19458207
PMCPMC2708400
OpenAlexW1996209042

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.