Transplantation-related complications predicted by cytokine gene expression in the mixed lymphocyte culture in allogeneic bone marrow transplants

Leuk Lymphoma. 1995 Sep;19(1-2):27-32. doi: 10.3109/10428199509059660.

Abstract

In this study, we have investigated cytokine (IL-1 beta, IL-2, IL-5, IL-6, IFN-gamma, TNF-alpha) and T cell surface molecule (IL-2 receptor, CD28, CTLA-4) gene expression in two way mixed lymphocyte cultures (MLC) enhanced by concanavalin A (ConA) to assess whether this is a useful predictive method for severe graft-versus-host disease (GVHD) and graft failure in allogeneic bone marrow transplantation (allo BMT) patients. Our present study revealed increased mRNA expression of IL-2, IL-5 and IFN-gamma using this assay in patients with delayed engraftment followed by graft failure and patients who developed grade III acute GVHD. Elevated IL-2 and IFN-gamma levels in MLC medium were also observed in these patients. Concerning T cell surface molecule gene expression in our modified MLC, IL-2 receptor gene expression was not altered so much in allo BMT patients, however, CD28 and CTLA-4 gene expression were elevated in patients with graft failure and severe acute GVHD. The elevated expression of cytokines (IL-2, IL-5 and IFN-gamma) and T cell surface molecules (CD28 and CTLA-4) mRNA in our modified MLC, in patients who developed severe lethal transplantation-related complications may suggest an important role for these molecules in inducing a strong alloresponse. Therefore, the detection of increased gene expression of those molecules, in our modified MLC system, appeared to be useful for predicting transplantation-related complications in allo BMT patients. In addition, this modified MLC assay may also be useful for the selection of the most compatible related and unrelated donors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / biosynthesis
  • Base Sequence
  • Bone Marrow Transplantation / adverse effects*
  • Bone Marrow Transplantation / immunology*
  • CD28 Antigens / biosynthesis
  • Cytokines / biosynthesis*
  • DNA Primers
  • Gene Expression*
  • Graft vs Host Disease / epidemiology
  • Graft vs Host Disease / immunology*
  • Humans
  • Lymphocyte Culture Test, Mixed*
  • Lymphocytes / immunology*
  • Molecular Sequence Data
  • Postoperative Complications / epidemiology
  • Postoperative Complications / immunology
  • Predictive Value of Tests
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • T-Lymphocytes / immunology
  • Transplantation, Homologous

Substances

  • Antigens, CD
  • CD28 Antigens
  • Cytokines
  • DNA Primers
  • RNA, Messenger