The neutrophil: the unnoticed threat in xenotransplantation?

BACKGROUND: Xenotransplantation offers one way to circumvent the widening gap between the demand for and supply of human organs for transplantation, and the pig is widely regarded as the donor animal most likely to prove appropriate. Most attention has focused on the adaptive immune response to xenogeneic tissue. However, there is optimism that it may soon be possible to overcome that hurdle. In this paper, we consider the possibility of the direct recognition of xenogeneic tissue by neutrophils. METHODS: We studied in vitro the interaction of human neutrophils with cultured porcine endothelial cells in assays of adhesion (both static and flow), activation on the basis of chemiluminescence, and diapedesis and chemotaxis using split-well chambers. RESULTS: Human neutrophils showed increased adhesiveness to porcine endothelium in both static and flow adhesion systems. While this did not activate the neutrophils at rest, in the presence of suboptimal concentrations of a parallel stimulus, phorbol myristate acetate, the interaction of human neutrophils with porcine endothelium caused a much greater respiratory burst than their interaction with controls. In addition, they showed greater diapedesis through porcine endothelium. Of greatest interest is the observation that porcine endothelium secretes a molecule that is chemotactic for human neutrophils. CONCLUSIONS: On the basis of these observations, we should consider the potential for neutrophil-mediated low-grade damage to xenografts emerging as a significant problem when others have been circumvented.

Anergic T cells exert antigen-independent inhibition of cell-cell interactions via chemokine metabolism.

Due to their ability to inhibit antigen-induced T-cell activation in vitro and in vivo, anergic T cells can be considered part of the spectrum of immunoregulatory T lymphocytes. Here we report that both murine and human anergic T cells can impair the ability of parenchymal cells (including endothelial and epithelial cells) to establish cell-cell interactions necessary to sustain leukocyte migration in vitro and tissue infiltration in vivo. The inhibition is reversible and cell-contact dependent but does not require cognate recognition of the parenchymal cells to occur. Instrumental to this effect is the increased cell surface expression and enzymatic activity of molecules such as CD26 (dipeptidyl-peptidase IV), which may act by metabolizing chemoattractants bound to the endothelial/epithelial cell surface. These results describe a previously unknown antigen-independent anti-inflammatory activity by locally generated anergic T cells and define a novel mechanism for the long-known immunoregulatory properties of these cells.