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Updated: Sep 18, 2025

An Adoptive Transfer Model of Rheumatoid Arthritis in Mice
Published on: June 6, 2025
Identifying Targets and Drugs for Rheumatoid Arthritis Stratified Therapy Using Mendelian Randomization and a
Yuqing Yan1, You Wu1, Yixuan Sun1
1Hubei Key Laboratory of Agricultural Bioinformatics, College of Informatics, Huazhong Agricultural University, Wuhan 430074, China.
Abstract:
The prevalence of rheumatoid arthritis (RA) subtypes, including seropositive and seronegative, is influenced by lifestyle factors and exhibits high heterogeneity, resulting in reduced drug efficacy. This study aims to identify cytokines mediating the effects of different lifestyles on RA subtypes and to discover new drugs for personalized treatment. Mendelian randomization revealed that three cytokines (MIP1b, SCGFb, and TRAIL) partially mediated the effects of different lifestyles on RA overall or its subtypes. The pretrained model, i.e., DrugBAN, predicted the probability of 723,000 small molecule drugs binding to these three targets. In molecules with high binding rates, we calculated the structural similarity between known drugs for RA and other drugs to screen for new drugs, followed by molecular docking and molecular dynamics simulations for validation. The results indicate that these targets had promising binding affinity with known drugs and other drugs with high similarity. Our findings may guide therapeutic approaches for heterogeneous RA patients with specific lifestyle habits.
Insights
Lifestyle factors influence rheumatoid arthritis (RA) subtypes. This study identified key cytokines and used AI to predict novel drugs for personalized RA treatment, improving drug efficacy for heterogeneous patient groups.
Area of Science:
- Immunology
- Pharmacology
- Genetics
Background:
- Rheumatoid arthritis (RA) presents diverse subtypes (seropositive, seronegative) influenced by lifestyle, leading to varied drug responses.
- High heterogeneity in RA impacts treatment efficacy, necessitating personalized therapeutic strategies.
Purpose of the Study:
- To identify specific cytokines that mediate the influence of lifestyle factors on RA subtypes.
- To discover novel drug candidates for personalized treatment of heterogeneous RA patients.
Main Methods:
- Mendelian randomization analysis to identify mediating cytokines (MIP1b, SCGFb, TRAIL).
- AI-driven prediction (DrugBAN) of small molecule drug binding to identified cytokine targets.
- Structural similarity analysis, molecular docking, and simulations to screen and validate potential new drugs.
Main Results:
- Three cytokines (MIP1b, SCGFb, TRAIL) were identified as partial mediators between lifestyle and RA subtypes.
- The AI model predicted high binding probabilities for numerous small molecules against these targets.
- Computational validation confirmed promising binding affinities for screened drugs, suggesting potential therapeutic utility.
Conclusions:
- Identified cytokine targets and computationally screened drugs offer a pathway for personalized RA therapy.
- Findings support tailored treatment approaches for RA patients based on lifestyle and disease subtype.
- This study provides a framework for leveraging AI and computational methods in drug discovery for complex diseases like RA.
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