Evidence mapPaperPMID 41973156Full record

ReviewJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2026

Rethinking MS Therapeutics: From Disease Pathogenesis Mechanisms to AI-Driven Drug Discovery.

Maryam Ziaei, Mohammadreza Sehhati, Mohammadreza Torabi, Nafiseh Esmaeil, Fahimeh Ghasemi

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In one paragraph

Review in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Maryam ZiaeiDepartment of Bioinformatics and Systems Biology, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Mohammadreza SehhatiDepartment of Bioinformatics and Systems Biology, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Mohammadreza TorabiDepartment of Bioinformatics and Systems Biology, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Nafiseh EsmaeilDepartment of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran. n_esmaeil@med.mui.ac.ir.ORCID http://orcid.org/0000-0001-7237-1984
Fahimeh GhasemiDepartment of Medical Biotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran. f_ghasemi@tums.ac.ir.ORCID http://orcid.org/0000-0001-9333-4699

Funding

Iran National Science Foundation 4040702Vice Chancellery for Research of Isfahan University of Medical Sciences 3403273
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disorder of the CNS, characterized by inflammation, demyelination, and progressive neurodegeneration. Disease progression involves four key interconnected stages: the activation of immune cells in peripheral lymph regions, the migration of autoreactive cells across the blood-brain barrier, demyelination, and an often incomplete remyelination response. Despite such significant therapeutic advances, major challenges remain in early diagnosis, patient stratification, and personalized intervention. Artificial intelligence has emerged as a powerful tool to address these challenges by integrating complex, multimodal data sets and uncovering patterns. This review provided a comprehensive overview of MS pathogenesis and evaluated current and emerging therapeutic strategies. Recent advances in applying AI-driven approaches to MS diagnosis, including MRI-based lesion detection, disease-activity prediction, and support for individualized prognosis, were also investigated. Additionally, generative and predictive computational frameworks that enable rapid drug development, repositioning, therapeutic target identification, and the rational design of new molecules with optimized safety and efficacy profiles in MS were reviewed. Finally, current limitations, ethical considerations, and barriers to clinical translation are discussed, emphasizing the need for high-quality datasets, standardized evaluation, and robust validation strategies. Synthesizing the emerging evidence, the current review highlights how AI-enabled methodologies are reshaping MS research, connecting molecular insights with clinical decision-making and opening new perspectives for more accurate diagnosis, deeper mechanistic understanding, and personalized therapeutic development.

Indexed as

Artificial IntelligenceDrug DiscoveryMultiple SclerosisAnimalsHumansArtificial intelligenceDiagnosisDrug designMultiple sclerosisPathogenesisTherapeutic approaches

Identifiers

What Socratic 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 Socratic graph.