Donor-derived regulatory dendritic cell infusion and early immunosuppressive drug withdrawal in living-donor liver transplantation: a phase I/IIa trial

Operational tolerance (OT) following complete immunosuppression withdrawal (ISW) is rare ( ~ 13%) in eligible adult liver transplant recipients when initiated 1-2-years post-transplant. Regulatory dendritic cells (DCregs) promote transplant tolerance in pre-clinical models and attenuate immune effector cells in humans. Here, we completed a first-in-human phase I/IIa trial (2-year recruitment; 5 ± 0.5 years follow-up) to evaluate the feasibility, safety and preliminary efficacy of pre-emptive donor-derived DCreg (ddDCreg) infusion 7-days pre-transplant in 15 prospective living-donor liver recipients. Two patients were excluded from analysis for reasons unrelated to the study. ISW began one year post-transplant in candidates with a quiescent/permissive protocol biopsy. ddDCreg infusions were safe, reproducible, and well-tolerated. One-year post-transplant, 8/13 patients were eligible for ISW, 4 achieved complete ISW, 3 remained off all immunosuppression for >1 year. These 3 remained drug-free for 3.0 ± 0.17-years, reflecting a 37.5% OT rate in ISW-eligible recipients. Given the exploratory nature of this trial, additional studies to evaluate efficacy are needed. ClinicalTrials.gov registration number NCT03164265.

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Publication Details

Journal
Nature Communications
Published
2026-04-17
DOI
https://doi.org/10.1038/s41467-026-71280-8
Primary Topic
Renal Transplantation Outcomes and Treatments
Type
article
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0.00

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article

Donor-derived regulatory dendritic cell infusion and early immunosuppressive drug withdrawal in living-donor liver transplantation: a phase I/IIa trial

A W Thomson, Erin Ables, Beth Elinoff, Yannis Hadjiyannis et al.
Nature Communications
Renal Transplantation Outcomes and Treatments
article

Donor-derived regulatory dendritic cell infusion and early immunosuppressive drug withdrawal in living-donor liver transplantation: a phase I/IIa trial

A W Thomson, Erin Ables, Beth Elinoff, Yannis Hadjiyannis, Mindi A. Styn, Camila Macedo, Adriana Zeevi, Alan F. Zahorchak, Douglas Landsittel, Lillian M. Tran, Swaytha R. Ganesh, Christopher B. Hughes, Fadi G. Lakkis, Diana M. Metes, Abhinav Humar
article en

Abstract

Operational tolerance (OT) following complete immunosuppression withdrawal (ISW) is rare ( ~ 13%) in eligible adult liver transplant recipients when initiated 1-2-years post-transplant. Regulatory dendritic cells (DCregs) promote transplant tolerance in pre-clinical models and attenuate immune effector cells in humans. Here, we completed a first-in-human phase I/IIa trial (2-year recruitment; 5 ± 0.5 years follow-up) to evaluate the feasibility, safety and preliminary efficacy of pre-emptive donor-derived DCreg (ddDCreg) infusion 7-days pre-transplant in 15 prospective living-donor liver recipients. Two patients were excluded from analysis for reasons unrelated to the study. ISW began one year post-transplant in candidates with a quiescent/permissive protocol biopsy. ddDCreg infusions were safe, reproducible, and well-tolerated. One-year post-transplant, 8/13 patients were eligible for ISW, 4 achieved complete ISW, 3 remained off all immunosuppression for >1 year. These 3 remained drug-free for 3.0 ± 0.17-years, reflecting a 37.5% OT rate in ISW-eligible recipients. Given the exploratory nature of this trial, additional studies to evaluate efficacy are needed. ClinicalTrials.gov registration number NCT03164265.

Nature CommunicationsVol. 17(1)
University of Pittsburgh (US), UPMC Health System (US), Indiana University Bloomington (US), University of Pittsburgh Medical Center (US), University at Buffalo, State University of New York (US)
Burroughs Wellcome Fund, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, University of Pittsburgh, National Institutes of Health, Medical Center, University of Pittsburgh, National Institute of Allergy and Infectious Diseases
Good health and well-being
Openalex Percentile: Top 23%
Renal Transplantation Outcomes and Treatments
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