Jul 2026· Journal of Medical Sciences· Vol 95, pp. e1565· 0 citations· 14 references
TL;DR
This review synthesises current insights into MS immunopathology and recent advances in B-cell-targeted therapies and CAR-T approaches, highlighting an evolving therapeutic landscape focused on improving disease control and long-term outcomes.
Abstract
Introduction. Multiple sclerosis (MS) is a chronic autoimmune disorder of the central nervous system (CNS) characterised by neuroinflammation and neurodegeneration leading to progressive disability. Its complex immunopathogenesis involves autoreactive T cells, B cells, and myeloid cells, with growing evidence highlighting the pivotal role of B lymphocytes. B cells contribute through antigen presentation, cytokine secretion, autoantibody production, and formation of ectopic lymphoid structures, making them key therapeutic targets. Current disease-modifying therapies (DMTs), including anti-CD20 monoclonal antibodies such as ocrelizumab, ofatumumab, and recently launched ublituximab, have significantly improved clinical outcomes. However, optimisation of long-term efficacy and safety remains challenging. The novel agent, frexalimab, which targets the CD40–CD40L pathway, aims to refine treatment precision and safety further.Material and methods. A systematic search of PubMed, Scopus, and Web of Science (October–November 2025) was conducted to identify clinical trials and high-quality reviews on emerging MS therapies, with emphasis on anti-CD20 agents, BTK inhibitors, frexalimab, and CAR-T therapy. Eligible studies were critically appraised for mechanisms of action, clinical efficacy, safety, and relevance, with particular focus on recent phase II–III data.Results. This review synthesises current insights into MS immunopathology and recent advances in B-cell-targeted therapies and CAR-T approaches, highlighting an evolving therapeutic landscape focused on improving disease control and long-term outcomes.Conclusions. Continued development of targeted immunotherapies may bring the field closer to sustained remission, effective prevention of progression, and potentially enhanced CNS repair.
Current evidence on advances in clinical research and immunotherapy across the major autoimmune CNS disease groups is synthesized, with a particular focus on trial designs, endpoints, and the evolution from observational cohorts to randomized controlled trials.
This review reframes MS immunotherapy through a tolerance-centric paradigm, distinguishing continuous maintenance disease-modifying therapies (DMTs) from immune reconstitution therapies (IRTs) from immune reconstitution therapies (IRTs) and emerging antigen-specific tolerance strategies.
Alireza Beheshti Maal, M. Arki, Seyed Massood Nabavi et al.· Neurological Sciences· 0 citations
A narrative review aims to synthesize recent findings, highlight emerging challenges, and provide practical insights for clinicians managing this complex interplay between uveitis and demyelinating diseases.
Aniruddha Agarwal, A. Mubashir, S. Mittal· Indian Journal of Ophthalmol...· 0 citations
Background: Autoimmune rheumatic diseases (ARDs) are characterized by a failure of immune tolerance, leading to chronic inflammation, autoantibody production, and progressive organ damage. Conventional therapies often fail to induce long-term, drug-free remission in refractory patients. Chimeric antigen receptor (CAR)...
Mateusz Miluski, D. Szydłowska, Mikołaj Jońca et al.· International Journal of Inn...· 0 citations
Current advances in the therapeutic landscape of progressive MS are summarized, highlighting recently approved treatments as well as promising agents under clinical investigation, with particular emphasis on the underlying mechanisms of action of these therapies and their potential to modify disease progression, restor...
Patients with central nervous system demyelinating disease (ICI-CDD) should be suspected in patients receiving ICI therapy who present with unexplained paraparesis, sensory deficits, sphincter dysfunction, visual loss, or visual field defects, thereby improving clinical outcomes.