Evidence map›Paper›PMID 34878645›Full record

ReviewThe British journal of dermatology2022

Antivascular endothelial growth factor-A therapy: a novel personalized treatment approach for psoriasis.

Andrea Luengas-Martinez, Ralf Paus, Helen S Young

Erratum issuedOpen access · greenAbstract readReview
In one paragraph

Review in The British journal of dermatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. The M2 Macrophages Importance Role in Psoriasis.Immunity, inflammation and disease · 2025
    Review
  7. Article
  8. Article
  9. Growth suppressing effect ofCytotechnology · 2025
    Article
  10. Neutrophils in tumor- and inflammation-induced lymphangiogenesis.International journal of biological sciences · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. The effect of secukinumab treatment for psoriasis on serum cytokines and correlation with disease severity.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 2 countries.

Andrea Luengas-MartinezCentre for Dermatology Research and Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.ORCID 0000-0003-1379-8675
Ralf PausCentre for Dermatology Research and Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.ORCID 0000-0002-3492-9358
Helen S YoungCentre for Dermatology Research and Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK.ORCID 0000-0003-1538-445X
Manchester Academic Health Science Centre · GBUniversity of Miami · US

Funding

British Skin Foundation R122088
6 · The paper itself

Abstract

Chronic plaque psoriasis is an inflammatory skin disease in which genetic predisposition along with environmental factors lead to the development of the disease, which affects 2% of the UK's population and is associated with extracutaneous morbidities and a reduced quality of life. A complex crosstalk between innate and adaptive immunity, the epithelia and the vasculature maintain the inflammatory milieu in psoriasis. Despite the development of promising treatment strategies, mostly targeting the immune system, treatments fail to fulfil every patient's goals. Vascular endothelial growth factor-A (VEGF-A) mediates angiogenesis and is upregulated in the plaques and plasma of patients with psoriasis. Transgenic expression of VEGF-A in experimental models led to the development of skin lesions that share many psoriasis features. Targeting VEGF-A in in vivo models of psoriasis-like inflammation resulted in disease clearance. Anti-angiogenesis treatments are widely used for cancer and eye disease and there are clinical reports of patients treated with VEGF-A inhibitors who have experienced Psoriasis Area and Severity Index improvement. Existing psoriasis treatments downregulate VEGF-A and angiogenesis as part of their therapeutic effect. Pharmacogenetics studies suggest the existence of different genetic signatures within patients with psoriasis that correspond with different treatment responsiveness and disease severity. There is a subset of patients with psoriasis with an increased predisposition to produce high levels of VEGF-A, who may be most likely to benefit from anti-VEGF-A therapy, offering an opportunity to personalize treatment in psoriasis. Anti-VEGF-A therapies may offer an alternative to existing anticytokine strategies or be complementary to standard treatments for the management of psoriasis.

Indexed as

PsoriasisVascular Endothelial Growth Factor AEndothelial Growth FactorsHumansNeovascularization, PathologicPrecision MedicineQuality of LifeEndothelial Growth FactorsVascular Endothelial Growth Factor A

Identifiers

PMID34878645
PMCPMC9313866
OpenAlexW4200319744

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.