Evidence map›Paper›PMID 21654633›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2011

Neither IL-17A mRNA nor IL-17A protein are detectable in Langerhans cell histiocytosis lesions.

Tricia L Peters, Kenneth L McClain, Carl E Allen

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Merkel cell polyomavirus and Langerhans cell neoplasm.Cell communication and signaling : CCS · 2018
    Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Langerhans-Cell Histiocytosis.The New England journal of medicine · 2018
    Review
  10. Observational
  11. Article
  12. Cell(s) of Origin of Langerhans Cell Histiocytosis.Hematology/oncology clinics of North America · 2015
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Is serum IL-17A a useful systemic biomarker in patients with Langerhans cell histiocytosis?Molecular therapy : the journal of the American Society of Gene Therapy · 2012
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Tricia L PetersTexas Children's Hospital Cancer Center and Hematology Service, Houston, Texas, USA.
Kenneth L McClain
Carl E Allen
Baylor College of Medicine · USTexas Children's Hospital · US

Funding

Redefining Langerhans Cell Histiocytosis as a Myeloid Dysplasia and Identifying BR01CA154489 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ALLEN, CARL E · 2011 to 2015
$1.6M
NCI NIH HHS R01 CA154489NIAID NIH HHS L40 AI076739
6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) is a rare disease characterized by heterogeneous lesions including CD207(+)/CD1a(+) dendritic cells that can result in significant morbidity and mortality. The etiology of LCH remains speculative, and neoplastic and inflammatory origins have been debated for decades. A recent study identified abundant interleukin-17 (IL-17A) protein in dendritic cells in LCH lesions as well as in plasma from patients with active disease. Furthermore, it identified dendritic cells as a novel source of IL-17A expression. However, subsequent studies from our research group failed to identify any IL-17A gene expression from CD207(+) dendritic cells or CD3(+) T cells in LCH lesions. In this study, further investigation once again fails to identify any cells in LCH lesions with IL-17A gene expression. Furthermore, IL-17A antigen is undetectable in LCH lesion lysates with western blotting, immunoprecipitation, spectral analysis, and enzyme-linked immunosorbent assay (ELISA). Western blots, immunoprecipitation, and ELISA experiments also demonstrate that antibodies used in original studies that established the IL-17A hypothesis for pathogenesis of LCH recognize nonspecific proteins. We conclude that evidence for IL-17A as a significant factor in LCH remains inadequate and clinical trials targeting IL-17A remain unjustified.

Indexed as

Antibodies, MonoclonalAntigens, CDAntigens, CD1Blotting, WesternDendritic CellsEnzyme-Linked Immunosorbent AssayHistiocytosis, Langerhans-CellHumansImmunoprecipitationInterleukin-17Lectins, C-TypeMannose-Binding LectinsReverse Transcriptase Polymerase Chain ReactionRNA, MessengerAntibodies, MonoclonalAntigens, CDAntigens, CD1CD1a antigenCD207 protein, humanInterleukin-17Lectins, C-TypeMannose-Binding LectinsRNA, Messenger

Identifiers

PMID21654633
PMCPMC3149162
OpenAlexW2028050596

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.