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Updated: Apr 27, 2026

Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Targets of new immunosuppressants in renal transplantation
Josep M Cruzado1, Oriol Bestard1, Eduardo Melilli1
1Department of Nephrology, Hospital Universitari de Bellvitge, University of Barcelona, IDIBELL, L'Hospitalet de Llobregat , Barcelona, Spain.
Abstract:
Although current immunosuppression is highly effective in avoiding acute rejection, it is associated with nephrotoxicity, cardiovascular morbidity, infection, and cancer. Thus, new drugs dealing with new mechanisms, as well as minimizing comorbidities, are warranted in renal transplantation. Few novel drugs are currently under investigation in Phase I, II, or III clinical trials. Belatacept is a humanized antibody that inhibits T-cell co-stimulation and has shown encouraging results in Phase II and III trials. Moreover, two new small molecules are under clinical development: AEB071 or sotrastaurin (a protein kinase C inhibitor) and CP-690550 or tasocitinib (a Janus kinase inhibitor). Refinement in selecting the best combinations for the new and current immunosuppressive agents is probably the main challenge for the next few years.
Insights
New immunosuppressive drugs are needed for renal transplantation to reduce side effects like organ damage and cancer. Novel agents such as belatacept, sotrastaurin, and tasocitinib show promise in clinical trials.
Area of Science:
- Nephrology
- Immunology
- Pharmacology
Background:
- Current immunosuppression in renal transplantation effectively prevents acute rejection but causes significant toxicities.
- These toxicities include nephrotoxicity, cardiovascular disease, increased infection risk, and cancer development.
- There is a critical need for novel immunosuppressive strategies with improved safety profiles.
Purpose of the Study:
- To review emerging immunosuppressive drugs for renal transplantation.
- To highlight novel mechanisms of action and ongoing clinical investigations.
- To discuss the challenges in optimizing immunosuppressive regimens.
Main Methods:
- Review of current clinical trials and investigational drugs in renal transplantation.
- Focus on agents targeting T-cell co-stimulation, protein kinase C, and Janus kinase pathways.
- Analysis of efficacy and safety data from Phase II and III trials.
Main Results:
- Belatacept, a T-cell co-stimulation inhibitor, demonstrates promising results in Phase II and III trials.
- Sotrastaurin (AEB071), a protein kinase C inhibitor, and tasocitinib (CP-690550), a Janus kinase inhibitor, are in clinical development.
- These novel agents offer alternative mechanisms to current immunosuppressants.
Conclusions:
- Novel immunosuppressive drugs are under investigation to overcome the limitations of current therapies.
- Optimizing combinations of new and existing agents presents a key challenge for future renal transplantation protocols.
- Further research is essential to refine immunosuppression and improve long-term patient outcomes.
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