What is the treatment for kidney transplant rejection?

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Last updated: June 21, 2025View editorial policy

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From the Guidelines

Treatment for kidney transplant rejection involves a combination of immunosuppressive medications, with the first-line treatment for acute rejection episodes being high-dose intravenous methylprednisolone. The standard approach to preventing rejection includes a combination therapy with calcineurin inhibitors, antiproliferative agents, and corticosteroids. According to the KDIGO clinical practice guideline for the care of kidney transplant recipients 1, induction therapy with a biologic agent, such as an IL2-RA, is recommended as part of the initial immunosuppressive regimen. For long-term maintenance, the guideline suggests using the lowest planned doses of maintenance immunosuppressive medications by 2–4 months after transplantation, if there has been no acute rejection 1.

The medications used in the treatment of kidney transplant rejection work by suppressing different aspects of the immune response. Calcineurin inhibitors, such as tacrolimus, block T-cell activation, while antiproliferatives, like mycophenolate mofetil, inhibit lymphocyte proliferation. Corticosteroids, such as prednisone, reduce inflammation and immune cell activity. The goal of these medications is to prevent the immune system from recognizing and attacking the transplanted kidney.

Key points in the treatment of kidney transplant rejection include:

  • Using a combination of immunosuppressive medications to prevent rejection
  • Starting induction therapy with a biologic agent, such as an IL2-RA, before or at the time of transplantation 1
  • Using high-dose intravenous methylprednisolone as the first-line treatment for acute rejection episodes
  • Considering T-cell depleting antibodies, plasma exchange, and intravenous immunoglobulin for steroid-resistant or antibody-mediated rejection
  • Regular monitoring of drug levels, kidney function, and signs of rejection to adjust the treatment plan as needed.

In terms of specific medications and dosages, tacrolimus (target trough levels 5-10 ng/mL), mycophenolate mofetil (1000mg twice daily), and prednisone (tapered to 5mg daily) are commonly used for long-term maintenance therapy. However, the exact treatment plan may vary depending on the individual patient's needs and response to therapy. It is essential to follow the guidelines and adjust the treatment plan according to the patient's condition and the latest evidence-based recommendations 1.

From the FDA Drug Label

THYMOGLOBULIN is indicated for the prophylaxis and treatment of acute rejection in patients receiving a kidney transplant. The recommended dosage of THYMOGLOBULIN for treatment of acute rejection in patients receiving a kidney transplant is 1.5 mg/kg of body weight administered daily for 7 to 14 days.

The treatment for kidney transplant rejection is THYMOGLOBULIN administered at a dosage of 1.5 mg/kg of body weight daily for 7 to 14 days. This should be used in conjunction with concomitant immunosuppression 2.

From the Research

Treatment Options for Kidney Transplant Rejection

The treatment for kidney transplant rejection typically involves immunosuppressive medications to reduce the immune system's attack on the transplanted kidney. The choice of treatment depends on the severity and type of rejection.

  • Immunosuppressive medications: These include calcineurin inhibitors (e.g., cyclosporin, tacrolimus), anti-proliferative agents (e.g., azathioprine, mycophenolate mofetil), and steroids (e.g., prednisolone) 3.
  • Pulse steroid treatment: This is often the first-line therapy for acute rejection, with a success rate of 60-70% 4.
  • Antilymphocytic antibodies: These are used to treat steroid-resistant rejection, with success rates of 60-70% 4.
  • Mycophenolate mofetil: This medication has been successfully used to treat steroid-resistant rejection, particularly of the interstitial (cellular) type 4.
  • Bortezomib-based regimen: This has been shown to be effective in treating antibody-mediated rejection, with a response rate of 67% in one study 5.
  • Plasmapheresis and intravenous immunoglobulin: These treatments have been used in some cases of severe antibody-mediated rejection, with surprising success 4, 6.
  • Antigen-specific immunoadsorption: This treatment has been used to successfully treat acute antibody-mediated rejection caused by ABO antibodies 6.

Considerations for Treatment

The treatment of kidney transplant rejection must be carefully balanced against the risks of infection, lymphoma, and other side effects. The choice of treatment will depend on the individual patient's circumstances and the severity of the rejection.

  • Monitoring and adjustment: The patient's immunosuppressive regimen may need to be adjusted to prevent further rejection or to minimize side effects 3, 4.
  • Close follow-up: Patients with a history of rejection will require close monitoring to detect any signs of further rejection or other complications 4, 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Steroid-resistant kidney transplant rejection: diagnosis and treatment.

Journal of the American Society of Nephrology : JASN, 2001

Research

Treatment of antibody-mediated rejection in kidney transplant recipients: a single-center experience with a bortezomib-based regimen.

Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation, 2012

Research

Acute antibody-mediated rejection after ABO-incompatible kidney transplantation treated successfully with antigen-specific immunoadsorption.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2010

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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