Evidence map›Paper›PMID 18431321›Full record

ArticleMinerva medica2008

Role of cytokine p40 family in multiple sclerosis.

S Brahmachari, K Pahan

Open access · greenAbstract read
In one paragraph

Article in Minerva medica, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Article
  3. Build muscles and protect myelin.NeuroImmune pharmacology and therapeutics · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. IL-12 p40 monomer is different from other IL-12 family members to selectively inhibit IL-12Rβ1 internalization and suppress EAE.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Can cinnamon spice down autoimmune diseases?Journal of clinical & experimental immunology · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Epstein-Barr virus-induced gene 3 (EBI3) can mediate IL-6The Journal of biological chemistry · 2017
    Article
  18. Article
  19. Review
  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

2 authors at 1 institution in 1 country.

S BrahmachariDepartment of Neurological Sciences, Rush University Medical Center, Chicago, IL 60612, USA.
K Pahan
Rush University Medical Center · US

Funding

ACTIVATION OF NF-KB IN GLIAL CELLS AND CNS OF EAER01NS039940 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PAHAN, KALIPADA · 2001 to 2009
$2.7M
Statin and Phenylacetate in MPTP Mouse ModelR21NS048923 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI PAHAN, KALIPADA · 2006 to 2007
$327k
NINDS NIH HHS NS 39940NINDS NIH HHS NS 48923NINDS NIH HHS R01 NS039940NINDS NIH HHS R21 NS048923
6 · The paper itself

Abstract

Over the last couple of decades of neuro-immunological research, the p40 family of cytokines has emerged out as one of the most intriguing areas of interest because of multi-faceted roles of these cytokine in immune-modulation and inflammation. The IL-12, the most widely studied cytokine of this family, is well-characterized for its Th1-favoring activity, and therefore plays a key role in the pathophysiology of Th1-mediated autoimmune diseases like multiple sclerosis (MS). On the other hand, the IL-23, another member of the p40 family with shared p40 subunit, drives polarization of Th17, a subset of T cell suspected to have a key role in the pathophysiology of MS and experimental allergic encephalomyelitis (EAE), poses a challenge to our current understanding of Th1/Th2 hypotheses in autoimmune diseases. However, the more puzzling issues, the researchers are currently confronted with, are the biological roles of other two members of this family, the p40 monomer and the p40(2), the homodimer. Predominance of the mRNA level of p40 over p35 in the central nervous system of EAE and MS suggests a possible involvement of p40 in the pathogenesis of MS. However, the distinctive biological role of monomeric and dimeric form of p40 is not clearly understood yet. Initially, it was thought that p402 does not have any biological activity and only involved in antagonizing bioactive IL-12 but according to recent evidences, both p402 and p40 appear to have a proinflammatory role, therefore might be a crucial molecule in the pathogenesis of MS. The current review focuses on biological function of p40 family of cytokines with particular emphasis on MS.

Indexed as

Encephalomyelitis, Autoimmune, ExperimentalEnzyme InductionHumansInterferon-gammaInterleukin-12Interleukin-12 Subunit p40Interleukin-23Multiple SclerosisNitric Oxide Synthase Type IIT-Lymphocyte SubsetsInterferon-gammaInterleukin-12Interleukin-12 Subunit p40Interleukin-23Nitric Oxide Synthase Type II

Identifiers

PMID18431321
PMCPMC2570259
OpenAlexW180656536

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.