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Tocilizumab Stabilizes Renal Function in Kidney Transplant Recipients with Chronic Active Antibody Mediated Rejection (CAAMR)

S. Patel, S. Mohan, H. Fernandez, I. Batal, L. Ratner, J. Crew.

Columbia University, New York.

Meeting: 2018 American Transplant Congress

Abstract number: 205

Keywords: Alloantibodies, Highly-sensitized, Rejection

Session Information

Session Name: Concurrent Session: Kidney Chronic Antibody Mediated Rejection

Session Type: Concurrent Session

Date: Monday, June 4, 2018

Session Time: 2:30pm-4:00pm

 Presentation Time: 2:42pm-2:54pm

Location: Room 4B

INTRO: CAAMR after kidney transplantation (KTx) is associated with rates of allograft failure approaching 50% at 2 years from injury involving T cells, B cells, and donor specific antibodies (DSA). Tocilizumab(TOC) is a monoclonal antibody that inhibitis IL-6, a regulator of T- and B- cell activation, and has been used to desensitize waitlisted patients. We report our experience using TOC in patients(pts) with CAAMR.

METHODS/RESULTS: Since 2015, 20 pts received TOC 8 mg/kg with >3 months follow up added to tacrolimus/mycophenolate/pred for CAAMR refractory to treatment. Mean age at KTx was 37±11.5 years, most were female (16), and received live donor KTx(14). All patients had prior AMR with DSA[mdash]Class I=4, Class II=9, Class I&II= 7 – that persisted despite plasmapheresis(9), IVIG at 2 gm/kg(11), rituximab(5). 16 patients also had prior ACR (borderline=9, 1A=3,1B=3, 2A=1). TOC was started an average 1648±1420 days after transplant, with a starting creatinine-=2.35±0.95, and given an average 323±281 days. In the 3 months prior to initiation of TOC, eGFR declined by 3.9 cc/min each month, compared to 0.05 cc/min each month on TOC(p= 0.008). Proteinuria also stabilized on TOC- initial urine protein:creatinine ratio (UPC) of 1.01(±1.1) vs 0.80 (±1.1) at f/u. Stabilization was not dependent on level or type of DSA, and nor did DSA change significantly during follow up. There were 3 ACRs (2- borderline & 1B=1) and one patient with recurrent AMR after stopping TOC that responded to re-initiation. There were 2 cases of BK viremia (0 nephropathy), 1 EBV viremia, and 1 hospitalization for pneumonia. Only one patient stopped due to infusion related reactions. There was 1 patient with primary nonfunction due to unresolving ATN+AMR and 2 graft failures (1 non-compliance and 1 progressive rejection).

CONCLUSION: CAAMR is difficult to treat and associated with high rates of graft failure. In a group of patients with CAAMR refractory to other treatments, addition of TOC to a regimen of tac/mycophenolate/prednisone stabilized eGFR the majority despite persistent DSA with few infectious complications.

CITATION INFORMATION: Patel S., Mohan S., Fernandez H., Batal I., Ratner L., Crew J. Tocilizumab Stabilizes Renal Function in Kidney Transplant Recipients with Chronic Active Antibody Mediated Rejection (CAAMR) Am J Transplant. 2017;17 (suppl 3).

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To cite this abstract in AMA style:

Patel S, Mohan S, Fernandez H, Batal I, Ratner L, Crew J. Tocilizumab Stabilizes Renal Function in Kidney Transplant Recipients with Chronic Active Antibody Mediated Rejection (CAAMR) [abstract]. https://atcmeetingabstracts.com/abstract/tocilizumab-stabilizes-renal-function-in-kidney-transplant-recipients-with-chronic-active-antibody-mediated-rejection-caamr/. Accessed May 16, 2025.

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