Evidence map›Paper›PMID 42295377›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

Emerging therapeutic strategies in multiple sclerosis: a focus on innovative and targeted approaches.

Husna Irfan Thalib, Sariya Khan, Sanha Sideeque, Taqiyah Zaheerullah Sheriff, Aleesha Muzammil, Fatma E Hassan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of 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

6 authors.

Husna Irfan ThalibGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia. Husnairfan2905@gmail.com.ORCID http://orcid.org/0009-0009-6361-6586
Sariya KhanGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.ORCID http://orcid.org/0009-0003-9809-872X
Sanha SideequeGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.ORCID http://orcid.org/0009-0008-9644-3370
Taqiyah Zaheerullah SheriffGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.ORCID http://orcid.org/0000-0002-9492-6140
Aleesha MuzammilGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.ORCID http://orcid.org/0009-0003-9121-0088
Fatma E HassanDepartment of Physiology, General Medicine Practice Program, Batterjee Medical College, Jeddah, 21442, Saudi Arabia.ORCID http://orcid.org/0000-0002-3985-8931

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is an immune-mediated disease of the central nervous system marked by damage to myelin and nerve cells. Current treatments help control inflammation but have limited success in progressive stages and repairing nerve damage. This review aims to summarize new therapies for MS that target both inflammation and neurodegeneration beyond traditional immunosuppressive drugs. We conducted a thorough literature search to summarize key findings from original studies, including clinical trials investigating novel MS treatments such as Bruton's tyrosine kinase (BTK) inhibitors, CAR T-cell therapy, vaccines targeting Epstein-Barr virus (EBV) and specific antigens, drugs promoting remyelination, monoclonal antibodies, stem cell therapy, sphingosine-1-phosphate receptor modulators, cytokine blockers, gut microbiome interventions, and nanotechnology-based drug delivery. Emerging therapeutic strategies in MS increasingly target mechanisms beyond conventional immunosuppression, including B-cell and microglial modulation, immune tolerance induction, remyelination, cytokine signaling, microbiome regulation, and enhanced central nervous system drug delivery. BTK inhibitors and S1P receptor modulators demonstrated anti-inflammatory activity in clinical trials, although some agents failed to show superiority over established therapies. Cell-based therapies, including CAR T-cell therapy and stem cell transplantation, showed early promise in refractory disease but remain limited by safety concerns and insufficient long-term data. Remyelination-promoting agents and EBV-targeted immunotherapies demonstrated encouraging preliminary findings; however, many approaches remain in preclinical or early-phase clinical stages. Nanotechnology-based delivery systems and microbiome-directed therapies represent emerging areas with potential translational relevance. Emerging therapies in MS reflect a growing shift toward mechanism-based and potentially personalized therapeutic strategies. Although several approaches demonstrate promising preclinical and early clinical results, many remain investigational, and further large-scale studies are required to establish long-term efficacy, safety, and clinical applicability.

Indexed as

Multiple SclerosisAnimalsDrug Delivery SystemsHumansImmunosuppressive AgentsMolecular Targeted TherapyImmunosuppressive AgentsBTK inhibitorsCAR T-cell therapyEBV vaccinesMesenchymal stem cellsMonoclonal antibodiesMSRemyelination

Identifiers

What OpenQuestion 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 OpenQuestion graph.