T regulatory cell therapy in transplantation: stability,... : Current Opinion in Organ Transplantation (original) (raw)

TOLERANCE INDUCTION: Edited by Fred Fändrich

stability, localization and functional specialization

aDepartments of Surgery

bPathology and Laboratory Medicine, University of British Columbia

cChild and Family Research Institute, Vancouver, British Columbia, Canada

Correspondence to Megan K. Levings, Child and Family Research Institute, 950 West 28th Ave, Vancouver, BC, V5Z 4H4, Canada. E-mail: [email protected]

Abstract

Purpose of review

There is great hope that cellular therapy with regulatory T cells (Tregs) will be an effective way to induce alloantigen specific tolerance, ultimately allowing for reduction or elimination of nonspecific immunosuppression. In the past, considerable effort was focused on defining the optimal ways to isolate and expand Tregs from peripheral or cord blood. Now that expansion of therapeutically relevant numbers of Tregs is feasible, we need to consider what is going to happen to the cells when they are transferred in vivo.

Recent findings

For optimal function, Tregs must be able to traffic to the correct location(s) and, despite the presence of immunosuppressive therapy, live long enough to transfer their regulatory function to recipient T cells. Within the Treg pool, there are also functionally specialized subsets, identified by chemokine receptor expression and/or cytokine production, which control their trafficking and relative ability to suppress different types of T helper cells, respectively. Recent findings imply that the plasticity of appropriately obtained populations of Tregs may not be of as great concern as previously suggested. Experimental data have also provided evidence as to how one might design adjunctive treatment that best supports the viability and function of Tregs after transfer.

Summary

Knowledge of how Tregs work in transplantation comes from studies that do not recapitulate how these cells will be used in humans. There is a need to develop better preclinical models to study how the in-vivo function of human Tregs can be optimized to ensure they can meet the challenge of inducing transplantation tolerance.