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Biologic agents for rheumatoid arthritis: can we hypothesize new strategies of treatment?
Alberto Migliore1, Eleonora Ballanti1, Bruno Laganà2
1Unit of Rheumatology, S. Pietro FBF Hospital, Research Center S. Pietro, Via Cassia 600, 00189 Rome, Italy.
Abstract:
Rheumatoid arthritis is a complex multifactorial disease, whose pathogenesis has not been fully elucidated. Biologic agents have revolutionized RA treatment, but a significant percentage of patients does not obtain an adequate response to the therapy. Most of the biologic agents do better if combined with conventional immunosuppressive DMARDs and they show a similar efficacy profile: most of the responders achieve the minimum desirable level of response (ACR20) and only few patients obtain a worthwhile clinical improvement (ACR70 or better). We need to identify new strategies of treatment, able to comply the non satisfied needs of RA patients. Taking inspiration from other medical fields, we could hypothesize a combined regimen in which biologic agents are administered simultaneously at a low or ultra-low dosage, targeting several pathogenetic mechanisms but avoiding important side effects. Alternatively it should be useful to identify rapid succession regimens in which biologic drugs are taken according to an established sequence. Research in this field is obviously not encouraged by pharmaceutical industries, but our efforts should be driven in this direction. According to these observations, adequate clinical trials should be designed to search for appropriate drugs associations and dosages.
Insights
New rheumatoid arthritis (RA) treatment strategies are needed as current biologics offer limited efficacy for many. Exploring combined low-dose or sequential biologic regimens may improve outcomes for RA patients.
Area of Science:
- Immunology
- Rheumatology
- Pharmacology
Background:
- Rheumatoid arthritis (RA) is a complex, multifactorial autoimmune disease.
- Biologic agents have transformed RA treatment but show suboptimal response rates in a significant patient subset.
- Current therapies often achieve only modest improvement (ACR20), with few reaching substantial clinical benefit (ACR70+).
Purpose of the Study:
- To address unmet needs in RA treatment by exploring novel therapeutic strategies.
- To investigate the potential of combined or sequential administration of biologic agents.
- To identify treatment regimens that target multiple pathogenic pathways while minimizing adverse effects.
Main Methods:
- Hypothesizing combined regimens of low or ultra-low dose biologic agents.
- Considering rapid succession regimens with sequential biologic drug administration.
- Emphasizing the need for clinical trials to validate these approaches.
Main Results:
- Current biologic therapies for RA demonstrate limited efficacy for a substantial proportion of patients.
- Combination with conventional disease-modifying antirheumatic drugs (DMARDs) offers marginal benefits.
- Few patients achieve significant clinical improvement with existing biologic treatments.
Conclusions:
- Novel treatment strategies are crucial for patients with RA who do not respond adequately to current therapies.
- Investigating simultaneous low-dose or sequential biologic regimens warrants further research.
- Clinical trials are essential to determine optimal drug combinations and dosages for improved RA management.
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