Evidence map›Paper›PMID 23994348›Full record

ArticleInternational immunopharmacology2013

Neuroimmune semaphorin 4A as a drug and drug target for asthma.

G Mogie, K Shanks, E H Nkyimbeng-Takwi, E Smith, E Davila, M M Lipsky, L J DeTolla, A D Keegan, S P Chapoval

Open access · greenAbstract read
In one paragraph

Article in International immunopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Semaphorins and Their Role in Neuropathic Pain.Life (Basel, Switzerland) · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Identifying Function Determining Residues in Neuroimmune Semaphorin 4A.International journal of molecular sciences · 2022
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Semaphorins 4A and 4D in chronic inflammatory diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2017
    Review
  14. Review
  15. Article
  16. Semaphorins and plexins as therapeutic targets.Nature reviews. Drug discovery · 2014
    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

9 authors at 2 institutions in 1 country.

G MogieCenter for Vascular and Inflammatory Diseases, Greenebaum Cancer Center, University of Maryland School of Medicine, Baltimore, MD, USA.
K Shanks
E H Nkyimbeng-Takwi
E Smith
E Davila
M M Lipsky
L J DeTolla
A D Keegan
S P Chapoval
U-M Rogel Cancer CenterUniversity of Maryland, Baltimore · US

Funding

Molecular Mechanisms of IL-4 and IL-13 SignalingR01AI038985 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI KEEGAN, ACHSAH D. · 2001 to 2010
$3.7M
Immune Semaphorins in Allergic Airway InflammationR21AI076736 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAPOVAL, SVETLANA P. · 2009 to 2010
$413k
NIAID NIH HHS R01 AI038985NIAID NIH HHS R21 AI076736NIAID NIH HHS R21AI076736
6 · The paper itself

Abstract

Neuroimmune semaphorin 4A (Sema4A) has been shown to play an important costimulatory role in T cell activation and regulation of Th1-mediated diseases such as multiple sclerosis (MS), experimental autoimmune encephalomyelitis (EAE), and experimental autoimmune myocarditis (EAM). Sema4A has three functional receptors, Tim-2 expressed on CD4+ T cells, Th2 cells in particular, and Plexin B1 and D1 predominantly expressed on epithelial and endothelial cells, correspondingly. We recently showed that Sema4A has a complex expression pattern in lung tissue in a mouse model of asthma. We and others have shown that corresponding Plexin expression can be found on immune cells as well. Moreover, we demonstrated that Sema4A-deficient mice displayed significantly higher lung local and systemic allergic responses pointing to its critical regulatory role in the disease. To determine the utility of Sema4A as a novel immunotherapeutic, we introduced recombinant Sema4A protein to the allergen-sensitized WT and Sema4A(-/-) mice before allergen challenge. We observed significant reductions in the allergic inflammatory lung response in Sema4A-treated mice as judged by tissue inflammation including eosinophilia and mucus production. Furthermore, we demonstrated that in vivo administration of anti-Tim2 Ab led to a substantial upregulation of allergic inflammation in WT mouse lungs. These data highlight the potential to develop Sema4A as a new therapeutic for allergic airway disease.

Indexed as

AllergensAnimalsAntibodiesAsthmaBronchoalveolar Lavage FluidCell CountCytokinesFemaleGranulocytesMaleMembrane ProteinsMiceMice, Inbred C57BLMice, KnockoutOvalbuminRecombinant ProteinsAllergensAntibodiesCytokinesMembrane ProteinsOvalbuminRecombinant ProteinsSema4A protein, mouseSemaphorinsTimd2 protein, mouseAsthmaIn vivoMouse modelRecombinant proteinSema4ATim-2

Identifiers

PMID23994348
PMCPMC3818409
OpenAlexW1984585276

What OpenQuestion holds

Textmetadata
LicenceTDM
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.