Summary:Hepatic dysfunction resulting from hepatic veno-occlusive disease (VOD) is a common complication of bone marrow transplantation (BMT). Some investigators believe that hepatic dysfunction, along with pulmonary and central nervous system (CNS) dysfunction, is part of a systemic disorder called multiple organ dysfunction syndrome (MODS). Endothelial damage by pretransplant chemo-radiation and activation of hemostasis are considered early events in the development of hepatic VOD. The pathological mechanism leading to fibrous obliteration of hepatic vessels may also take place in pulmonary and CNS vessels. Since antiphospholipid antibodies (aPA) are associated with venous and arterial thrombosis, which can lead to vessel occlusion, we asked if the incidence of aPA before conditioning was greater in patients who developed MODS following BMT. Samples drawn before pretransplant chemo-radiation from 57 patients who subsequently developed MODS and 55 control patients who did not develop MODS were studied blindly for aPA by ELISA. The number of aPA-positive patients who developed MODS (10/57), compared to the number of aPA-positive patient controls who did not develop MODS (7/55) was not statistically significant (P = 0.48). Our data indicate that the incidence of aPA before conditioning was not greater in patients who developed MODS, including hepatic VOD, following BMT. Keywords: antiphospholipid antibodies; anticardiolipin antibodies; autoimmunity; thrombosis; hepatic veno-occlusive disease; multiple organ dysfunction syndrome Hepatic dysfunction resulting from hepatic veno-occlusive disease (VOD) is a common, often fatal complication of bone marrow transplantation (BMT). Endothelial damage due to pretransplant chemo-radiation and activation of hemostasis are considered to be early events in the development of hepatic VOD with the end result being fibrous obliteration of hepatic vessels.1 The deposits of fibrin and factor VIII in hepatic vessels 2 are consistent with the decreased functional levels of protein C and antithrombin III (ATIII) in patients who develop hepatic VOD subsequent to transplantation.