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Update on Phase 2 Clinical Trial To Induce Tolerance in Mismatched Living Donor Renal Transplant Recipients

J. Leventhal, M. Abecassis, J. Miller, L. Gallon, K. Ravindra, D. Tollerud, B. King, M. Elliott, G. Herzig, R. Herzig, S. Ildstad

Northwestern University, Chicago, IL
Institute for Cellular Therapeutics, University of Louisville, Louisville, KY
James Graham Brown Cancer Ctr, University of Louisville, Louisville, KY
Regenerex, LLC, Louisville, KY

Meeting: 2013 American Transplant Congress

Abstract number: 549

19 subjects have been enrolled in a phase 2 protocol (FDA IDE 13947) to induce tolerance in mismatched recipients of living donor renal allografts (KTx). The protocol is based upon tolerogenic CD8+/TCR– facilitating cells (FC) and nonmyeloablative conditioning. Recipients were conditioned with fludarabine (30 mg/kg/dose, days -5, -4, -3), cyclophosphamide (50 mg/kg/dose, day -3 and +3), 200 cGy TBI (day -1) followed by KTx (day 0). A G-CSF mobilized peripheral blood mononuclear cell product was apheresed from the donor > 2 weeks prior to the KTx, processed to remove GVHD-producing cells yet retain CD34+ cells and FC, and cryopreserved until administration to the recipient on day +1 post-KTx. Subjects ranged in age from 18 to 65 years. All were HLA-disparate from their donors, ranging from 5 of 6 matched related to 0 of 6 unrelated. 18 of 19 subjects exhibited engraftment at 1 month; one highly sensitized subject (PRA > 50%) did not engraft. Subjects were discharged on post-operative day 2 and managed as outpatients. Mycophenolate mofetil and tacrolimus-based immunosuppression was weaned and discontinued at 1 year if chimerism, normal renal function and normal kidney biopsy were noted. No subjects have experienced GVHD or engraftment syndrome. Two early subjects who received a suboptimal cell dose and one other highly sensitized subject were only transiently chimeric (< 6 months); all transiently chimeric subjects resumed endogenous hematopoiesis and are maintained on low-dose tacrolimus monotherapy with stable renal function. One subject developed viral sepsis at month 3, thrombosed his kidney, and was successfully re-transplanted off study. The remaining subjects are either off all immunosuppression (n = 8; 1 to 26 months) or are in the process of tapering. None of the chimeric subjects have developed rejection on protocol biopsy while 3 of the 5 who were not durably chimeric had Banff 1A rejection on protocol biopsy. In summary, high levels of durable chimerism and tolerance without GVHD have been achieved in mismatched related and unrelated recipients of living KTx.

Tollerud, D.: Other, Regenerex, LLC, Officer. King, B.: Employee, Regenerex, LLC. Ildstad, S.: Other, Regenerex, LLC, CEO.

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To cite this abstract in AMA style:

Leventhal J, Abecassis M, Miller J, Gallon L, Ravindra K, Tollerud D, King B, Elliott M, Herzig G, Herzig R, Ildstad S. Update on Phase 2 Clinical Trial To Induce Tolerance in Mismatched Living Donor Renal Transplant Recipients [abstract]. Am J Transplant. 2013; 13 (suppl 5). https://atcmeetingabstracts.com/abstract/update-on-phase-2-clinical-trial-to-induce-tolerance-in-mismatched-living-donor-renal-transplant-recipients/. Accessed May 10, 2025.

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