Evidence map›Paper›PMID 26605642›Full record

ReviewMolecular medicine (Cambridge, Mass.)2015

Once Upon a Time: The Adaptive Immune Response in Atherosclerosis--a Fairy Tale No More.

Marie Le Borgne, Giuseppina Caligiuri, Antonino Nicoletti

Open access · goldAbstract readReview
In one paragraph

Review in Molecular medicine (Cambridge, Mass.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. IntermedinCell death & disease · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. 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

3 authors at 1 institution in 1 country.

Marie Le BorgneUnité 1148, Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Xavier Bichat, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France; Département Hospitalo-Universitaire DHU FIRE, Paris, France.
Giuseppina CaligiuriUnité 1148, Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Xavier Bichat, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France; Département Hospitalo-Universitaire DHU FIRE, Paris, France.
Antonino NicolettiUnité 1148, Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Xavier Bichat, Paris, France; Université Paris Diderot, Sorbonne Paris Cité, Paris, France; Département Hospitalo-Universitaire DHU FIRE, Paris, France.
Hôpital Xavier Arnozan · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive research has been carried out to decipher the function of the adaptive immune response in atherosclerosis, with the expectation that it will pave the road for the design of immunomodulatory therapies that will prevent or reverse the progression of the disease. All this work has led to the concept that some T- and B-cell subsets are proatherogenic, whereas others are atheroprotective. In addition to the immune response occurring in the spleen and lymph nodes, it has been shown that lymphoid neo-genesis takes place in the adventitia of atherosclerotic vessels, leading to the formation of tertiary lymphoid organs where an adaptive immune response can be mounted. Whereas the mechanisms orchestrating the formation of these organs are becoming better understood, their impact on atherosclerosis progression remains unclear. Several potential therapeutic strategies against atherosclerosis, such as protective vaccination against atherosclerosis antigens or inhibiting the activation of proatherogenic B cells, have been proposed based on our improving knowledge of the role of the immune system in atherosclerosis. These strategies have shown success in preclinical studies, giving hope that they will lead to clinical applications.

Indexed as

Adaptive ImmunityAdventitiaAnimalsAtherosclerosisAutoantigensBlood VesselsB-Lymphocyte SubsetsCytokinesHumansImmunity, InnateImmunologic FactorsLymph NodesMiceSpleenT-Lymphocyte SubsetsVaccinationAutoantigensCytokinesImmunologic Factors

Identifiers

PMID26605642
PMCPMC4661052
OpenAlexW2408222629

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.