| Literature DB >> 23763435 |
O Bestard1, E Crespo, M Stein, M Lúcia, D L Roelen, Y J de Vaal, M P Hernandez-Fuentes, L Chatenoud, K J Wood, F H Claas, J M Cruzado, J M Grinyó, H D Volk, P Reinke.
Abstract
Assessment of donor-specific alloreactive memory/effector T cell responses using an IFN-γ Elispot assay has been suggested to be a novel immune-monitoring tool for evaluating the cellular immune risk in renal transplantation. Here, we report the cross-validation data of the IFN-γ Elispot assay performed within different European laboratories taking part of the EU RISET consortium. For this purpose, development of a standard operating procedure (SOP), comparisons of lectures of IFN-γ plates assessing intra- and interlaboratory assay variability of allogeneic or peptide stimuli in both healthy and kidney transplant individuals have been the main objectives. We show that the use of a same SOP and count-settings of the Elispot bioreader allow low coefficient variation between laboratories. Frozen and shipped samples display slightly lower detectable IFN-γ frequencies than fresh samples. Importantly, a close correlation between different laboratories is obtained when measuring high frequencies of antigen-specific primed/memory T cell alloresponses. Interestingly, significant high donor-specific alloreactive T cell responses can be similarly detected among different laboratories in kidney transplant patients displaying histological patterns of acute T cell mediated rejection. In conclusion, assessment of circulating alloreactive memory/effector T cells using an INF-γ Elispot assay can be accurately achieved using the same SOP, Elispot bioreader and experienced technicians in kidney transplantation. © Copyright 2013 The American Society of Transplantation and the American Society of Transplant Surgeons.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23763435 DOI: 10.1111/ajt.12285
Source DB: PubMed Journal: Am J Transplant ISSN: 1600-6135 Impact factor: 8.086