Evidence map›Paper›PMID 17671648›Full record

ArticleThe Journal of clinical investigation2007

New TB vaccines: is there a requirement for CD8 T cells?

W Henry Boom

Abstract readComment
In one paragraph

Article in The Journal of clinical investigation, 2007. 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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

W Henry BoomTuberculosis Research Unit, Case Western Reserve University and University Hospitals' Case Medical Center, Cleveland, Ohio 44106-4984, USA. whb@case.edu

Funding

HETEROGENEITY OF TCELLS IN M TUBERCULOSIS INFECTIONR01AI027243 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY · 1989 to 2016
$5.5M
MYCOBACTERIUM TUBERCULOSIS INFECTION IN THE LUNGR01HL055967 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI BOOM, W. HENRY · 1995 to 2010
$4.2M
NHLBI NIH HHS HL55967NHLBI NIH HHS R01 HL055967NIAID NIH HHS AI27243NIAID NIH HHS N01 AI070022NIAID NIH HHS R01 AI027243PHS HHS HHSN266200700022C
6 · The paper itself

Abstract

MHC class I-restricted CD8(+) T cells are necessary to mount an immune response against Mycobacterium tuberculosis. M. tuberculosis antigens can enter MHC class I cross-processing pathways through a number of different mechanisms, including via the uptake of antigen-containing apoptotic vesicles released by infected cells. A study in this issue of the JCI by Hinchey and colleagues shows that M. tuberculosis inhibits host cell apoptosis and thus may interfere with optimal cross-priming and action of CD8(+) T cells (see the related article beginning on page 2279). M. tuberculosis genetically modified to induce apoptosis is shown to be more effective in priming CD8(+) T cells in vivo and therefore may be a more effective vaccine against tuberculosis than the currently utilized M. bovis BCG vaccine.

Indexed as

Adenosine TriphosphatasesBacterial ProteinsGene DeletionMembrane Transport ProteinsAnimalsCell LineGuinea PigsHumansMacrophagesMiceMice, Inbred BALB CMycobacterium bovisMycobacterium tuberculosisSuperoxide DismutaseTuberculosisTuberculosis VaccinesAdenosine TriphosphatasesBacterial ProteinsMembrane Transport ProteinsSecA2 protein, MycobacteriumSuperoxide DismutaseTuberculosis Vaccines

Identifiers

PMID17671648
PMCPMC1934597

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.