Evidence map›Paper›PMID 22531914›Full record

ArticleEuropean journal of immunology2012

CBA/J mice generate protective immunity to soluble Ag85 but fail to respond efficiently to Ag85 during natural Mycobacterium tuberculosis infection.

Gillian L Beamer, Joshua Cyktor, David K Flaherty, Paul C Stromberg, Bridget Carruthers, Joanne Turner

Abstract read
In one paragraph

Article in European journal of immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Mitochondrial Transplantation Promotes Protective Effector and Memory CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  5. Extracellular Delivery of Functional Mitochondria Rescues the Dysfunction of CD4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. 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

6 authors.

Gillian L BeamerCenter for Microbial Interface Biology, The Ohio State University, Columbus, OH, USA.
Joshua Cyktor
David K Flaherty
Paul C Stromberg
Bridget Carruthers
Joanne Turner

Funding

MOUSE PATHOBIOLOGY: MODELS OF HUMAN DISEASET32RR007073 · NCRR · OHIO STATE UNIVERSITY · PI ROSOL, THOMAS J · 2002 to 2011
$3.2M
Immune correlates of reactivation tuberculosisR01AI064522 · NIAID · OHIO STATE UNIVERSITY · PI TURNER, JOANNE · 2007 to 2012
$2.0M
Chemokines and their receptors in the pathogenesis of tuberculosisK08AI071111 · NIAID · OHIO STATE UNIVERSITY · PI BEAMER, GILLIAN L · 2007 to 2010
$492k
NCRR NIH HHS T32 RR007073NCRR NIH HHS T32 RR07073NIAID NIH HHS K08 AI071111NIAID NIH HHS N01 AI040091NIAID NIH HHS R01 AI064522
6 · The paper itself

Abstract

In CBA/J mice, susceptibility to Mycobacterium tuberculosis (M.tb) is associated with low interferon-gamma (IFN-γ) responses to antigens (Antigen 85 (Ag85) and early secreted antigenic target-6 (ESAT-6)) that have been defined as immunodominant. Here, we asked whether the failure of CBA/J mice to recognize Ag85 is a consequence of M.tb infection or whether CBA/J mice have a general defect in generating specific T-cell responses to this protein antigen. We compared CBA/J mice during primary M.tb infection, Ag85 vaccination followed by M.tb challenge, or M.tb memory immune mice for their capacity to generate Ag85-specific IFN-γ responses and to control M.tb infection. CBA/J mice did not respond efficiently to Ag85 in the context of natural infection or re-infection. In contrast, CBA/J mice could generate Ag85-specific IFN-γ responses and protective immunity when this antigen was delivered as a soluble protein. Our data indicate that although M.tb infection of CBA/J mice does not drive an Ag85 response, these mice can fully and protectively respond to Ag85 if it is delivered as a vaccine. The data from this experimental model suggest that the Ag85-containing vaccines in clinical trials should protect M.tb susceptible humans.

Indexed as

AnimalsAntigens, BacterialDisease Models, AnimalHumansImmunologic MemoryInterferon-gammaMiceMycobacterium tuberculosisT-LymphocytesTuberculosisVaccinationAntigens, BacterialInterferon-gamma

Identifiers

PMID22531914
PMCPMC3641789

What OpenQuestion holds

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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.