Very late antigen 1 blockade markedly promotes survival of corneal allografts

Objective: To investigate the role of very late antigen 1 ( VLA-1) ( also known as integrin receptor alpha(1)beta(1)) in corneal transplantation inflammation and allograft survival. Methods: Cell infiltration and vasculogenesis ( both angiogenesis and lymphangiogenesis) associated with allodisparate corneal transplantation were assessed in VLA-1-deficient conditions and controls by immunofluorescent microscopic studies. Corneal allograft survival was also assessed after anti-VLA-1 antibody treatment and in VLA-1 knockout recipient mice. Results: Anti-VLA-1 antibody treatment leads to a profound reduction in the granulocytic, monocytic, and T-cell infiltration after corneal transplantation. In addition, corneal angiogenesis and lymphangiogenesis were both significantly suppressed in VLA-1 knockout mice. Remarkably, universal graft survival was observed in both anti VLA-1 antibody treatment and knockout mice. Conclusions: Very late antigen 1 blockade markedly reduces inflammation and inflammation-induced tissue responses, including vasculogenic responses, associated with corneal transplantation and promotes allograft survival. Clinical Relevance: These studies offer insights into important integrin-mediated mechanisms of corneal transplant - related inflammation and provide possible new integrin-based immunotherapies for transplant rejection.