Evidence map›Paper›PMID 42191896›Full record

ArticleActa pharmacologica Sinica2026

T cell-targeted immunotherapies for multiple sclerosis: molecular mechanisms to therapeutic perspectives from Traditional Chinese medicine.

Meiling Wu, Shenyu Yan, Lu Zhang, Wen-Ting Li, Qiaohui Du, Jiangang Shen

Abstract read
PubMed Publisher
In one paragraph

Article in Acta pharmacologica Sinica, 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.

Meiling Wu *School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Shenyu Yan *School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Lu ZhangSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Wen-Ting LiDepartment of Pharmacy, The Eighth Affiliated Hospital, Sun Yat-Sen University, Shenzhen, 518033, China.
Qiaohui DuSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China.
Jiangang ShenSchool of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, 999077, China. shenjg@hku.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) is a chronic inflammatory demyelinating disorder of the central nervous system characterized by an imbalance between effector T cells (Th1/Th17) and regulatory T-cell (Treg) function. Current disease-modifying therapies (DMTs) reduce relapse frequency mainly through broad immunomodulation, but their non-specific mechanisms often lead to adverse effects and incomplete disease control, especially in progressive MS. These limitations have driven efforts to develop next-generation T-cell-targeted approaches, such as antigen-specific tolerance induction and adoptive Treg therapy. However, the highly oxidative inflammatory microenvironment within the central nervous system (CNS) of MS limits the development of these advanced T-cell-targeted therapies. Excessive reactive oxygen and nitrogen species (ROS/RNS) destabilize FoxP3 expression, interfere with IL-2 signaling, and promote Th17 differentiation, thereby reducing the stability and function of therapeutic T cells. This review summarizes the development of existing DMTs and emerging T-cell-targeted immunotherapies and reviews the current understanding of the underlying mechanisms. We further summarize evidence on bioactive compounds derived from Traditional Chinese Medicine (TCM) that can regulate ROS/RNS levels, reduce oxidative and inflammatory stress, and potentially serve as adjunct agents to improve the performance of cell-targeted therapies. In conclusion, we propose that future therapeutic strategies for MS may require the simultaneous targeting of autoreactive T-cell pathways and modulation of the CNS redox environment to maintain immune tolerance. Taken together, integrating T-cell immunotherapy with redox microenvironment modulation may enhance the durability of therapeutic responses and provide a conceptual rationale for combining TCM-based redox strategies with emerging cellular immunotherapies in the management of autoimmune neurological disorders.

Indexed as

multiple sclerosisoxidative stressT cellsTraditional Chinese Medicine

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.