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Trans-vivo Delayed Type Hypersensitivity Assay for Antigen Specific Regulation
Published on: May 2, 2013
Rabbit antithymocyte globulin. A 10-year experience in cardiac transplantation
J G Copeland1, T B Icenogle, R J Williams
1Department of Cardiology, University of Arizona, Tucson 85724.
Summary
Rabbit antithymocyte globulin improves cardiac transplant outcomes. This immunosuppressive agent, when combined with cyclosporine, steroids, and azathioprine, significantly reduces rejection and infection rates, enhancing patient survival.
Area of Science:
- Immunology
- Cardiology
- Transplantation Medicine
Background:
- Rabbit antithymocyte globulin (rATG) is an investigational immunosuppressive agent for T-cell depletion.
- Long-term clinical experience with rATG in cardiac transplantation is limited.
- Comparative data with other immunosuppressive agents like horse antithymocyte globulin and OKT3 is needed.
Purpose of the Study:
- To review the 10-year experience with rabbit antithymocyte globulin in cardiac transplant recipients.
- To evaluate the efficacy and safety of different immunosuppression protocols involving rATG.
- To identify an optimal immunosuppressive induction therapy for cardiac transplantation.
Main Methods:
- Retrospective analysis of 155 non-bridge-to-transplant cardiac recipients.
- Patients divided into three groups based on immunosuppression protocols from 1979 to 1989.
- Group I: rATG, steroids, azathioprine; Group II: rATG, cyclosporine, steroids; Group III: rATG, cyclosporine, steroids, azathioprine.
Main Results:
- Group III demonstrated superior 1- and 3-year survival rates (94% and 88%, respectively).
- Group III showed improved freedom from rejection (30% at 1 year) and infection (50% at 1 year).
- Significant reduction in early bacterial, viral, and nocardial infections observed in Group III compared to Group I.
Conclusions:
- A combination of rabbit antithymocyte globulin, cyclosporine, steroids, and azathioprine is an effective immunosuppressive induction strategy.
- This protocol leads to favorable survival rates and reduced infectious complications in cardiac transplant recipients.
- Current protocol using rATG (200 mg IM for 3 days) shows minimal toxicity and significant T-cell reduction.

