| Literature DB >> 26228897 |
I R Badell1, W H Kitchens1, M E Wagener1, A E Lukacher2, C P Larsen1, M L Ford1.
Abstract
Recent studies have shown that the quantity of donor-reactive memory T cells is an important factor in determining the relative heterologous immunity barrier posed during transplantation. Here, we hypothesized that the quality of T cell memory also potently influences the response to costimulation blockade-based immunosuppression. Using a murine skin graft model of CD8(+) memory T cell-mediated costimulation blockade resistance, we elicited donor-reactive memory T cells using three distinct types of pathogen infections. Strikingly, we observed differential efficacy of a costimulation and integrin blockade regimen based on the type of pathogen used to elicit the donor-reactive memory T cell response. Intriguingly, the most immunosuppression-sensitive memory T cell populations were composed primarily of central memory cells that possessed greater recall potential, exhibited a less differentiated phenotype, and contained more multi-cytokine producers. These data, therefore, demonstrate that the memory T cell barrier is dependent on the specific type of pathogen infection via which the donor-reactive memory T cells are elicited, and suggest that the immune stimulation history of a given transplant patient may profoundly influence the relative barrier posed by heterologous immunity during transplantation. © Copyright 2015 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Keywords: T cell biology; basic (laboratory) research/science; costimulation; fusion proteins and monoclonal antibodies: adhesion molecule specific; fusion proteins and monoclonal antibodies: costimulation molecule specific; immunobiology; immunosuppressant; immunosuppression/immune modulation; translational research/science
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Year: 2015 PMID: 26228897 PMCID: PMC5416935 DOI: 10.1111/ajt.13399
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086