Evidence map›Paper›PMID 22069732›Full record

ReviewToxins2011

T cell targeting by anthrax toxins: two faces of the same coin.

Silvia Rossi Paccani, Cosima T Baldari

Open access · goldAbstract readReview
In one paragraph

Review in Toxins, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Compartmentalized Cyclic AMP Production by theFrontiers in immunology · 2018
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
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

2 authors at 2 institutions in 1 country.

Silvia Rossi PaccaniDepartment of Evolutionary Biology, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy. silvia.rossi_paccani@novartis.com
Cosima T Baldari
Novartis (Italy) · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacillus anthracis, similar to other bacterial pathogens, has evolved effective immune evasion strategies to prolong its survival in the host, thus ensuring the unchecked spread of the infection. This function is subserved by lethal (LT) and edema (ET) toxins, two exotoxins produced by vegetative anthrax bacilli following germination of the spores. The structure of these toxins and the mechanism of cell intoxication are topics covered by other reviews in this issue. Here we shall discuss how B. anthracis uses LT and ET to suppress the immune defenses of the host, focusing on T lymphocytes, the key players in adaptive immunity. We shall also summarize recent findings showing that, depending on its concentration, ET has the ability not only to suppress T cell activation but also to promote the polarization of CD4(+) T cells to the Th2 and Th17 subsets, highlighting the potential use of this toxin as an immunomodulator.

Indexed as

Antigens, BacterialBacillus anthracisBacterial ToxinsChemotaxisCytokinesHost-Pathogen InteractionsHumansLymphocyte ActivationMicrofilament ProteinsNeoplasm ProteinsReceptors, Cell SurfaceReceptors, PeptideT-Lymphocytesanthrax toxinanthrax toxin receptorsAntigens, BacterialANTXR1 protein, humanANTXR2 protein, humanBacterial ToxinsCytokinesMicrofilament ProteinsNeoplasm ProteinsReceptors, Cell SurfaceReceptors, PeptidecAMPedema toxinimmunodeviatingimmunosuppressionlethal toxinMAP kinasesT cellTCR signalingTh subset

Identifiers

PMID22069732
PMCPMC3202842
OpenAlexW2036340348

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.