Cutting edge: Immunological consequences and trafficking of human regulatory macrophages administered to renal transplant recipients

Regulatory macrophages (M regs) were administered to two living-donor renal transplant recipients. Both patients were minimized to low-dose tacrolimus monotherapy within 24 wk of transplantation and subsequently maintained excellent graft function. After central venous administration, most M regs re...

Full description

Bibliographic Details
Main Authors: Hutchinson, J, Riquelme, P, Sawitzki, B, Tomiuk, S, Miqueu, P, Zuhayra, M, Oberg, H, Pascher, A, Lützen, U, Janßen, U, Broichhausen, C, Renders, L, Thaiss, F, Scheuermann, E, Henze, E, Volk, H, Chatenoud, L, Lechler, R, Wood, K, Kabelitz, D, Schlitt, H, Geissler, E, Fändrich, F
Format: Journal article
Language:English
Published: 2011
Description
Summary:Regulatory macrophages (M regs) were administered to two living-donor renal transplant recipients. Both patients were minimized to low-dose tacrolimus monotherapy within 24 wk of transplantation and subsequently maintained excellent graft function. After central venous administration, most M regs remained viable and were seen to traffic from the pulmonary vasculature via the blood to liver, spleen, and bone marrow. By 1 y posttransplantation, both patients displayed patterns of peripheral blood gene expression converging upon the IOT-RISET signature. Furthermore, both patients maintained levels of peripheral blood FOXP3 and TOAG-1 mRNA expression within the range consistent with nonrejection. It is concluded that M regs warrant further study as a potential immune-conditioning therapy for use in solid-organ transplantation. The results of this work are being used to inform the design of The ONE Study, a multinational clinical trial of immunomodulatory cell therapy in renal transplantation. Copyright © 2011 by The American Association of Immunologists, Inc.