Efficacy and Safety of Tocilizumab in Treatment of Acute Antibody Mediated Rejection
Transplant Nephrology, Washington University, Saint Louis, MO
Transplant Nephrology, Ohio State University, Columbus, OH
Transplant Nephrology, Washington University, Saint Louis, MO
Transplant Nephrology, Washington University, Saint Louis, MO.
Meeting: 2018 American Transplant Congress
Abstract number: A117
Keywords: Antibodies, Outcome, Rejection, Renal function
Session Information
Session Name: Poster Session A: Kidney Acute Antibody Mediated Rejection
Session Type: Poster Session
Date: Saturday, June 2, 2018
Session Time: 5:30pm-7:30pm
Presentation Time: 5:30pm-7:30pm
Location: Hall 4EF
Antibody mediated rejection continues to be one of the most detrimental complications of kidney transplant. Multiple therapeutic strategies focused on B cell and/or HLA antibody removal are used with conflicting reports regarding efficacy. Tocilizumab (TCZ), an IL-6 inhibitor, has shown promising results in downregulating humoral immunity in patients with chronic antibody mediated rejection (AMR). Its efficacy has not been examined in the treatment of acute AMR. We present the case of 5 patients with acute AMR who received Tocilizumab therapy between Oct 2016 – Jun 2017. All patients were sensitized with history of prior transplant, rejection and/or pre-transplant cPRA of 100%, and had evidence of high DSA MFIs at the time of biopsy. Patients received treatment with IV Solumedrol, IVIG and increasing tacrolimus trough target to 10-12 ng/ml. 1 patient received rituximab, 2 patients received Thymoglobuin and 1 patient received a dose of eculizuamb for TMA like features on kidney biopsy. TCZ 8 mg/kg monthly infusion therapy was started during treatment for acute rejection episode and continued for a duration of 3-6 months. Renal function improved in all 5 patients. DSAs decreased significantly in 4 patients and remained stable in the 5th. Tocilizumab therapy was discontinued in 3 patients due to complications including CMV disease and severe allergic reaction. Severe combined cellular and AMR occurred 7 months post discontinuation in one patient.
PATIENT | AGE | RACE | IMMUNODOMINANT DSA (iDSA) | Pre-TCZ DSA iDSA MFI | Post-TCZ iDSA MFI | Cr at time of ABMR | Cr 3 mon post rejection |
1 | 42 | African American | DQB5*01:01 | 23477 | 11580 | 2.92 | 1.70 |
2 | 67 | Caucasian | DQA1* 06:01/ DQB1*01:01 | 21663 | 6344 | 1.8 | 1.2 |
3 | 35 | Caucasian | DRB5*01:01 | 5346 | 1089 | 1.49 | 0.7 |
4 | 35 | Asian | B*51:02 | 16864 | 5013 | 5.69 | 2.02 |
5 | 39 | African American | DRB1*13:03 | 22923 | 5515 | 2.1 | 1.5 |
The addition of TCZ to acute AMR treatment strategy appears to be effective and needs further validation.
CITATION INFORMATION: Venkatachalam K., Reem D., Andrew M., Delos Santos R., Alhamad T. Efficacy and Safety of Tocilizumab in Treatment of Acute Antibody Mediated Rejection Am J Transplant. 2017;17 (suppl 3).
To cite this abstract in AMA style:
Venkatachalam K, Reem D, Andrew M, Santos RDelos, Alhamad T. Efficacy and Safety of Tocilizumab in Treatment of Acute Antibody Mediated Rejection [abstract]. https://atcmeetingabstracts.com/abstract/efficacy-and-safety-of-tocilizumab-in-treatment-of-acute-antibody-mediated-rejection/. Accessed November 21, 2024.« Back to 2018 American Transplant Congress