ABSTRACT
The knowledge of systemic inflammation and local cytokine expression in porcine endocarditis models is limited, though it could provide valuable information about the pathogenesis and comparability to human endocarditis. Analyses of bacteriology and hematology were performed on blood samples from pigs with non-bacterial thrombotic endocarditis (NBTE, n = 11), Staphylococcus aureus infective endocarditis (IE, n = 2), animals with S. aureus sepsis without endocarditis (n = 2) and controls (n = 2). Furthermore, immunohistochemistry was used to examine the local expression of IL-1ß and IL-8. Bacterial blood cultures were continuously positive in IE pigs from inoculation to euthanasia, and negative in all other pigs at all times. The total white blood cell counts and total neutrophil counts were massively elevated in pigs with IE. Local IL-1ß and IL-8 expression in IE pigs were moderate to high, and high, respectively. In addition, slight local expression of IL-1ß and IL-8 was present in some NBTE pigs. In the IE model, both the systemic inflammatory response and the high local expression of IL-8 were comparable to the human disease. Furthermore, the results indicate IL-1ß and IL-8 as important contributors in the endocarditis pathogenesis.
Subject(s)
Endocarditis, Bacterial/complications , Endocarditis, Bacterial/immunology , Endocarditis, Non-Infective/complications , Endocarditis, Non-Infective/immunology , Interleukin-1beta/metabolism , Interleukin-8/metabolism , Staphylococcal Infections/complications , Staphylococcal Infections/immunology , Systemic Inflammatory Response Syndrome/etiology , Systemic Inflammatory Response Syndrome/immunology , Animals , Disease Models, Animal , Endocarditis, Bacterial/blood , Endocarditis, Non-Infective/blood , Female , Humans , Immunohistochemistry , Leukocyte Count , Myocardium/immunology , Myocardium/pathology , Sepsis/blood , Sepsis/immunology , Staphylococcal Infections/blood , Sus scrofa , Systemic Inflammatory Response Syndrome/bloodABSTRACT
Non-bacterial endocarditis lesions associated with antiphospholipid antibodies (aPLs) in the absence of other criteria for antiphospholipid syndrome or systemic lupus erythematosus is termed an aPL-associated cardiac valve disease. Evidence regarding the management of this condition is sparse. A rare case is described of a 20-year-old female who presented with an incidental finding of 'vegetations on a heart valve'. Echocardiography revealed mitral valve leaflet thickening and echodensities with moderate mitral regurgitation. She had an elevated partial thromboplastin time that did not correct with a mixing study, and elevated levels of antiocardiolipin antibodies. Hence, a diagnosis of aPL-associated cardiac valve disease was made, and the patient commenced on warfarin, hydroxychloroquine, and a short course of oral prednisone. At one year after diagnosis the patient remained symptom-free, and follow up echocardiography revealed resolution of the vegetations with minimal mitral regurgitation. Further evidence is needed to guide the therapy of this rare condition.