ijms-logo

Journal Browser

Journal Browser

Unraveling Neuroimmune Disorders: From Pathogenic Pathways to Biomarker-Driven Precision Medicine

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Immunology".

Deadline for manuscript submissions: 20 May 2026 | Viewed by 842

Special Issue Editor


E-Mail Website
Guest Editor
1. Dipartimento di Medicina e Chirurgia Traslazionale, Sezione di Patologia Generale, Università Cattolica del Sacro Cuore, 00168 Rome, Italy
2. Fondazione Policlinico Universitario “A. Gemelli” IRCCS, 00168 Rome, Italy
Interests: immunology; autoimmunity; inflammation; biomarkers
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Neuroimmune disorders represent a huge burden for society. The pathogenetic mechanisms arise from the complexity of interactions between the immune system dysregulated or autoimmune response that, through autoantibodies and/or neuroimmune-related cells (T cells, B cells, neutrophils, and macrophages), mediates inflammatory damage targeting central or peripheral nervous system. Prominent examples of neuroimmune disorders encompass multiple sclerosis, miasthenia gravis, and neuromyelitis optica. In these conditions, inflammation, the long arm of innate immunity, may be considered the mediator of the final effects of deregulation. Neuroinflammatory and neurodegenerative disorders including Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis show dysregulated neuroimmune and inflammatory responses, with the activation of neurons, glial cells, and infiltration of peripheral immune cells into the brain thanks to a circuit involving proinflammatory cytokines, chemokines, and neurotoxic mediators.

Accordingly, besides the assessment of specific autoantibodies when the autoantigen is known, cellular and molecular biomarkers are largely involved in the diagnosis, prognosis, response to therapies, and follow-up for a prediction of changes in disease activity. Taking into account the individual and genetic susceptibility as well as the wide range of environment risk factors that concur with the pathogenesis, the importance of research to set up and validate novel, effective, and personalized biomarkers of neuroimmune conditions stands alone. This Special Issue is devoted to the most recent results aimed at exploiting the clinical potential of biomarkers measuring the disordered immune response.

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

  • Innate immunity;
  • Adaptive immunity;
  • Inflammation;
  • Autoantibodies;
  • Peptides;
  • Cytokines;
  • Receptors;
  • Leukocytes;
  • Extracellular vesicles;
  • Signal transduction;
  • Apoptosis.

Dr. Mariapaola Marino
Guest Editor

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 250 words) can be sent to the Editorial Office for assessment.

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. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. 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.

Keywords

  • innate immunity
  • adaptive immunity
  • inflammation
  • autoantibodies
  • peptides
  • cytokines
  • receptors
  • leukocytes
  • extracellular vesicles
  • signal transduction
  • apoptosis

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • Reprint: MDPI Books provides the opportunity to republish successful Special Issues in book format, both online and in print.

Further information on MDPI's Special Issue policies can be found here.

Published Papers (1 paper)

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

Research

11 pages, 1626 KB  
Article
GFAP, CHI3L1 and GCIPL Thickness as Baseline Predictors of Early Disability Progression in MS
by Ion Iulian Enache, Vlad Eugen Tiu, Cătălina Andreea Anghel, Cristina Tiu, Alina Popa-Cherecheanu, Mihai Bostan, Sonia Scippa, Alessia Balestrieri, Giovanni Smaldone and Andrea Soricelli
Int. J. Mol. Sci. 2025, 26(24), 11774; https://doi.org/10.3390/ijms262411774 - 5 Dec 2025
Viewed by 505
Abstract
Disability accumulation in multiple sclerosis often occurs independent of relapses and inflammatory activity, yet reliable predictors for early progression remain limited. Our aim was to evaluate the utility of baseline fluid and optical coherence tomography (OCT) biomarkers for predicting early disability progression in [...] Read more.
Disability accumulation in multiple sclerosis often occurs independent of relapses and inflammatory activity, yet reliable predictors for early progression remain limited. Our aim was to evaluate the utility of baseline fluid and optical coherence tomography (OCT) biomarkers for predicting early disability progression in newly diagnosed relapsing–remitting MS (RRMS). We performed a monocentric observational cohort study on 72 RRMS patients that were enrolled within 6 months of diagnosis and followed for 2 years. Baseline serum and cerebrospinal fluid (CSF) samples were analyzed for neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP) and chitinase-3-like protein 1 (CHI3L1). Confirmed disability progression at 1 year (1yCDP) was defined by either an increase in Expanded Disability Status Scale or a ≥20% worsening on Nine-Hole Peg Test or Timed 25-Foot Walk. Seventeen patients (23.6%) developed 1yCDP. Elevated baseline CSF GFAP (OR = 5.79, 95% CI 1.72–19.45; p = 0.005) and CSF CHI3L1 thickness (OR = 4.14, 95% CI 1.49–11.49; p = 0.006) and reduced ganglion cell-inner plexiform layer (GCIPL) thickness (OR = 0.90, 95% CI 0.84–0.97; p = 0.006) independently predicted 1yCDP. A multivariate model including age, CSF GFAP and GCIPL achieved AUC = 0.831, with a sensitivity of 87.5% and specificity of 61.5%. This study provides evidence that baseline patient profiling using CSF GFAP, CSF CHI3L1 and GCIPL thickness may help predict early disability progression in RRMS. Full article
Show Figures

Figure 1

Back to TopTop