Alex S. Befeler
University of Chicago
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Featured researches published by Alex S. Befeler.
Transplantation | 1999
Alex S. Befeler; Thomas D. Schiano; Trevor W. Lissoos; Hari Conjeevaram; Allen S. Anderson; J. Michael Millis; Mario Albertucci; Alfred L. Baker
BACKGROUND Three patients received liver/heart transplantation, and we report their successful outcome. METHODS Two patients had alcoholic cirrhosis and dilated cardiomyopathy; one had cryptogenic liver disease and idiopathic cardiomyopathy. RESULTS All patients had evidence of portal hypertension and coagulopathy. The cardiac transplants were performed first. Cardiopulmonary bypass was discontinued in favor of venovenous bypass, and liver transplantation was then performed. All patients developed acute tubular necrosis; two required a brief period of hemodialysis. There was only one episode of acute cellular rejection of the liver. Protocol endomyocardial biopsies in all three patients revealed no evidence of rejection. All patients are currently using low doses of immunosuppressive medications and have normal liver chemistry tests and cardiac function; two patients have mild renal insufficiency. CONCLUSION In selected patients with severe cardiac dysfunction and advanced liver disease, liver/heart transplantation can be successfully performed even in the face of portal hypertension and coagulopathy.
Gastroenterology | 2010
Sombat Treeprasertsuk; Peter L. M. Jansen; Kris V. Kowdley; Velimir A. Luketic; M. Edwyn Harrison; Timothy M. McCashland; Alex S. Befeler; Denise M. Harnois; Roberta A. Jorgensen; Jeff Schmoll; Tanya L. Hoskin; Prabin Thapa; Felicity Enders; Keith D. Lindor
Background/Aims: There has been increased interest in the potential role of B cells and antimitochondrial antibodies in PBC. Indeed a new paradigm in PBC includes the potential of B cells to act as both regulatory elements and as components of the inflammasone induced by apoptosis of biliary cells. We submit that a rigorous dissection of the inflammatory infiltrate in PBC will provide further insight on these issues. Materials and Methods: We took advantage of well-characterized Mabs to CD3, CD4, CD8, CD20, CD38, CD56, CD68, and pan-keratin antigens, and immunohistochemistry (IHC), to study the distribution of liver infiltrating CD38-positive plasma cells in 26 consecutive patients with PBC (AMA positive in 20 and negative in 6), all of whom had detailed staged clinical data. All data was “blindly” evaluated. We simultaneously studied 10 ageand gender-matched patients with chronic hepatitis C as a control. Results: Noteworthy within the IHC data was the presence of an intense coronal arrangement (CR) of CD38-positive cells around interlobular bile ducts, generally in specimens with chronic non-suppurative destractive cholangitis (CNSDC). In contrast, CD20-positive B lymphocytes (precursor cells of plasma cells) were found scattered and/or aggregated within the lymphoplasmocytic infiltration. Such CD20positive B cells also occasionally formed follicle-like aggregations but importantly were not observed in the proximity of CNSDC. PBC patients with CR demonstrated significantly higher titers of AMA (119.5±16.1 vs. 59.7±17.1, p=0.018) and lower levels of total cholesterol (TC) (195.1±9.0 vs. 223.6±9.6, p=0.04) than those without CR. Interestingly the CR correlated with titer of AMA (r=0.46), IgM (r=0.32), the presence of CNSDC (r=0.32) and inversely with age (r=-0.37), γ-GTP (r=-0.38) and TC (r=-0.41). In contrast, CD4and CD8-positive T lymphocyte infiltration was noted either in proximity of, or within the degenerated cholangioepithelium, suggesting the participation of these cells in the destructive processes of interlobular bile ducts. No CR was found in control subjects. Conclusion: The presence of CD38+ plasma cells surrounding biliary epithelium has clinical and serologic significance; further it correlates with disease progression exemplified by TC decrease and the development of florid duct lesions. These data further highlight the functional significance of B cells/ plasma cells; it also reflects a multilineage loss of tolerance in PBC. We submit that study of B cells in PBC should go beyond simple measurement of AMA titer and include rigorous phenotypical and functional dissection of the liver specific B cell lineage populations.
Gastroenterology | 2010
Alina M. Allen; Youssef Assioun; Alex S. Befeler; John M. Richart; Adrian M. Di Bisceglie
A S L D A b st ra ct s better survival in cirrhotic patients with huge HCC (P 15 cm., vascular invasion and distant metastasis were poor prognostic factor by univariate analysis while tumor size (HR 8.4, 95%CI 1.6-44.9) and distant metastasis (HR 8.5, 95%CI 2.5-75.6) were significantly predicted poor outcomes in multivariate analysis (P 15 cm. and distant metastasis were associated with poor outcomes in non-cirrhotic group.
Archives of Surgery | 2005
Alex S. Befeler; Dean E. Palmer; Martin Hoffman; Walter E. Longo; Harvey Solomon; Adrian M. Di Bisceglie
Transplantation | 1998
Alex S. Befeler; Trevor W. Lissoos; Thomas D. Schiano; Hari Conjeevaram; Kathy Dasgupta; J. Michael Millis; Kenneth A. Newell; J. Richard Thistlethwaite; Alfred L. Baker
Transplantation | 1999
Hari Conjeevaram; John Hart; Trevor W. Lissoos; Thomas D. Schiano; Kathy Dasgupta; Alex S. Befeler; J M Millis; Alfred L. Baker
Archive | 2010
Adrian M. Di Bisceglie; Alex S. Befeler
Archive | 2014
Elie Chahla; Muhammad B. Hammami; Alex S. Befeler
Gastroenterology | 2018
Muhammad B. Hammami; Amanda Cheung; Matthew Stotts; David Westrich; Armani Patel; Eric C. Anderson; Lauren R. Counts; Alexa Fider-Whyte; Adrian M. Di Bisceglie; Alex S. Befeler; Charlene M. Prather
Gastroenterology | 2016
Wei Zhang; Alireza Shams; Alex S. Befeler; Ningling Kang; Jinping Lai