A Phase I/II Trial of the Interleukin-6 Receptor–Specific Humanized Monoclonal (Tocilizumab) + Intravenous Immunoglobulin in Difficult to Desensitize Patients. Issue 11 (November 2015)

• Record Type: Journal Article
• Authors: Vo, Ashley A.; Choi, Jua; Kim, Irene; Louie, Sabrina; Cisneros, Kristen; Kahwaji, Joseph; Toyoda, Mieko; Ge, Shili; Haas, Mark; Puliyanda, Dechu; Reinsmoen, Nancy; Peng, Alice; Villicana, Rafael; Jordan, Stanley C.
• Is Part Of: Transplantation. Volume 99:Issue 11(2015)
• Publication Date: 2015-11
• Subjects: Transplantation of organs, tissues, etc -- Periodicals; Transplantation immunology -- Periodicals; 617.95
• DOI: 10.1097/TP.0000000000000741
• Languages: English
• ISSNs: 0041-1337

Abstract

Abstract : Background: Current desensitization (DES) methods are not always effective. Thus, novel, more effective approaches are desirable. Interleukin (IL)-6 is an attractive target as it promotes B-cell differentiation to plasma cells, is important for immunoglobulin production, and induces Th17 cells. Here, we undertook a phase I/II pilot study of DES using a novel drug (anti–IL-6 receptor (IL-6R), Tocilizumab [TCZ]) + intravenous Ig (IVIg) to assess safety and limited efficacy. Methods: From July 2012 to November 2013, 10 patients unresponsive to DES with IVIg + Rituximab were treated with IVIg + TCZ. Patients received IVIg on days 0 and 30 at 2 g/kg and TCZ 8 mg/kg on day 15 then monthly for 6 months. If transplanted, patients received IVIg once and TCZ monthly for 6 months. Results: No differences in baseline characteristics were seen in patients not transplanted versus transplanted. Two patients in each group developed serious adverse events: not transplanted- pulmonary congestion with epilepticus (likely not related) versus transplanted infective colitis with colonic perforation and Bell Palsy (both possibly related). Five of 10 patients were transplanted. Mean time to transplant from first DES was 25 ± 10.5 months but after TCZ was 8.1 ± 5.4 months. Six-month protocol biopsies showed no antibody-mediated rejection. Donor-specific antibody strength and number were reduced by TCZ treatment. Renal function at 12 months was 60 ± 25 mL/min. Conclusions: Tocilizumab and IVIg appear to be safe. From this pilot trial, we are cautiously optimistic that targeting the IL-6/IL-6R pathway could offer a novel alternative for difficult to desensitize patients. Larger controlled studies are essential to prove efficacy. Abstract : This phase I/II pilot study in 10 sensitized patients suggests that the use of anti-IL-6 receptor antagonist, tocilizumab, combined with IVIG is safe, reduces DSA strength and number and waiting time to kidney transplantation, and prevents antibody mediated rejection. Supplemental digital content is available in the text.