The Role of Semaphorins and Other Signaling Molecules in Inflammatory Rheumatic Diseases

A special issue of Biomolecules (ISSN 2218-273X). This special issue belongs to the section "Molecular Medicine".

Deadline for manuscript submissions: closed (31 December 2020) | Viewed by 2413

Special Issue Editors


E-Mail Website
Guest Editor
Rheumatology, Department of Medicine and Surgery, University of Perugia, p.le Menghini 1, 06129 Perugia, Italy
Interests: inflammatory arthritis; connective tissue diseases; systemic lupus erythematosus; Sjogren's syndrome; rare diseases in rheumatology
Special Issues, Collections and Topics in MDPI journals

E-Mail Website
Co-Guest Editor
Lupus Clinic, Reumatologia, Dipartimento di Scienze Cliniche Internistiche Anestesiologiche e Cardiovascolari, Sapienza Università di Roma, Rome, Italy
Interests: autoimmune diseases; systemic lupus erythematosus; genetic factors; pathogenic mechanisms; biomarkers
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Rheumatic diseases (RDs) are a heterogeneous cluster of pathological conditions, characterized by cellular and humoral immune responses, leading to an inflammatory milieu, with the production of pro-inflammatory cytokines. Musculo-skeletal manifestations represent a shared aspect that appear together with several clinical features that range from skin to renal involvement to the production of a large variety of autoantibodies.

One of the most important unmet needs in RDs consists of the identification of biomarkers able to identify patients at risk to develop more aggressive phenotypes and to predict response to treatment. In the last few years, some research has suggested a possible role for neural markers, such as semaphorin-3A (Sema3A), calcitonin gene-related peptide, nerve growth factor, and substance P, in immune response regulation. They are a large family of secreted or membrane-bound proteins, interacting with specific receptors. These neuropeptide pathways could stimulate well-defined changes in the activity and function of bone cells, leading to RD features.

For instance, Sema3A seems to exert a potent immunomodulator effect throughout the different stages of immune response by acting on T- and B-cells but also on FoxP3+ Tregs. This wide range of action strongly suggests a pivotal role for semaphorins in RD pathogenesis and the possibility to target these molecules as a therapeutic strategy. Data from the literature have so far provided contrasting results in terms of semaphorin serum levels in autoimmune diseases. Considering Sema3A, high levels of this molecule have been identified in patients affected by systemic lupus erythematosus, while low levels have been observed in patients with rheumatoid arthritis. Moreover, Sema3A seems to be contributing to bone remodeling in patients affected by spondyloarthropathies.

Nonetheless, neuropeptides seem to be involved in the pain modulation of patients affected by fibromyalgia, suggesting a possible role in disease pathogenesis and treatment.

The aim of this Special Issue is to summarize the latest knowledge and novel findings on the role of neuropeptides in RDs. We encourage basic scientists as well as clinicians to submit original research articles describing novel findings, as well as review articles summarizing the state of the art on neuropeptides in pathogenesis and as biomarkers and therapeutic targets in RDs.

Potential topics include, but are not limited to, the following:

  • The role of neuropeptides in the pathogenesis of RDs;
  • Genetic variants of neuropeptides in RDs;
  • The potential role of neuropeptides in RD therapy;
  • Neuropeptide modulation during the treatment of RDs.

Papers are published upon acceptance, regardless of the Special Issue publication date.

Dr. Carlo Perricone
Dr. Fulvia Ceccarelli
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Biomolecules is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

8 pages, 3236 KiB  
Article
The Expression of IL-17, in Chronic Spontaneous Urticaria Is Linked to Semaphorin5A
by Matanis Lobna, Eiza Nasren, Sabag Adi, Bejar Jacob, Gimenez-Arnau Ana Maria, Maurer Marcus and Vadasz Zahava
Biomolecules 2021, 11(3), 373; https://0-doi-org.brum.beds.ac.uk/10.3390/biom11030373 - 02 Mar 2021
Cited by 5 | Viewed by 1878
Abstract
Background: Patients with chronic spontaneous urticaria (CSU), an autoimmune disorder, show increased skin expression of IL-17A and can benefit from treatment with the anti-IL-17A biologic secukinumab. The mechanisms that drive IL-17A expression in CSU are currently unknown, but may involve Semaphorin5A (Sema5A). Objective: [...] Read more.
Background: Patients with chronic spontaneous urticaria (CSU), an autoimmune disorder, show increased skin expression of IL-17A and can benefit from treatment with the anti-IL-17A biologic secukinumab. The mechanisms that drive IL-17A expression in CSU are currently unknown, but may involve Semaphorin5A (Sema5A). Objective: To explore the expression, role, and effects of Sema5A in CSU and its link to IL-17A. Material and Methods: We investigated patients with CSU and healthy controls for skin expression of expressing peripheral T cells. Results: Sema5A was highly expressed in the skin of CSU patients as compared to healthy control skin. Both CD4+ T cells and mast cells in CSU skin expressed Sema5A, and many of them expressed both Sema5A and IL-17A. Patients with CSU had significantly higher rates of IL-17A-expressing CD4+ T cells as compared to healthy controls. Incubation with Sema5A increased the rates of IL-17A-expressing CD4+ T cells in healthy controls to CSU levels. Conclusion: Sema5A may drive the expression and effects of IL-17A in CSU. Further studies in larger cohorts are needed to confirm the role of Sema5A in the pathogenesis of CSU and to explore its potential as a therapeutic target. Full article
Show Figures

Figure 1

Back to TopTop