Allogeneic T cell expansion is the primary determinant of graft-versus-host disease (GVHD). The current understanding is that this expansion is driven by histocompatibility antigen disparities between donor and recipient. This paradigm represents a closed genetic system where donor T cells interact with peptide-major histocompatibility complexes (MHCs).
Graft versus host disease (GVHD) is a post-transplant condition where donor T cells attack recipient tissues, traditionally viewed as an immunological issue requiring immunosuppressive treatment
Graft-Versus-Host Disease (GVHD) is traditionally divided into an acute and a chronic disease (see also: Graft-Versus-Host Disease (GVHD) & Forms)
Graft-versus-host disease (GVHD) occurs when immunocompetent T cells in the graft recognize the recipient as foreign tissue and initiate the Immune Responses
All APCs massively present antigens (self and nonself) to the mature donor’s T cells, thereby activating invasion and damage.
Chronic graft-versus-host disease (GVHD), a major complication of allogeneic stem-cell transplantation, becomes glucocorticoid-refractory or glucocorticoid-dependent in approximately 50% of patients.
GVHD occurs when alloreactive T cells transplanted from a non-identical donor recognize the transplant recipient as foreign. This recognition triggers an immune response that damages the recipient's tissues. Acute GVHD is associated with allo-HCT in 40-50% of cases.
see also:
Allogeneic hematopoietic stem cell transplantation (allo HSCT)
Allogeneic hematopoietic stem cell transplantation (allo HSCT) & Gut microbiota