TIGIT safeguards liver regeneration through regulating natural killer cell‐hepatocyte crosstalk

Jiacheng Bi, Xiaodong Zheng, Yongyan Chen, Haiming Wei, Rui Sun, Zhigang Tian – 9 June 2014 – Overactivation of innate immunity, particularly natural killer (NK) cells, is harmful to liver regeneration; however, the molecular mechanisms that limit NK cell overactivation during liver regeneration are still elusive. Here we show that a coinhibitory receptor, T cell Ig and ITIM domain (TIGIT), was selectively up‐regulated on NK cells, along with high expression of its ligand, poliovirus receptor (PVR/CD155), on hepatocytes during liver regeneration.

Pharmacodynamic monitoring of immunosuppressive effects indicates reduced cyclosporine activity during telaprevir therapy

Katja Roos, Daniel Gotthardt, Thomas Giese, Paul Schnitzler, Wolfgang Stremmel, David Czock, Christoph Eisenbach – 3 June 2014 – Drug interactions with immunosuppressive drugs are a major problem associated with protease inhibitor–based antiviral triple therapy for hepatitis C virus (HCV) reinfection after liver transplantation. In this retrospective cohort study, we analyzed biomarkers of the immunosuppressive effects of cyclosporine A (CSA) by quantifying nuclear factor of activated T cells (NFAT)–regulated gene expression during telaprevir (TVR) therapy in 5 liver transplant patients.

Selection of a right posterior sector graft for living donor liver transplantation

Tomoharu Yoshizumi, Toru Ikegami, Koichi Kimura, Hideaki Uchiyama, Tetsuo Ikeda, Ken Shirabe, Yoshihiko Maehara – 3 June 2014 – Right posterior sector (RPS) grafts have been used to overcome graft size discrepancies, the major concern of living donor liver transplantation. Previous studies have reported the volumetry‐based selection of RPS grafts without anatomical exclusion. We reviewed our data and established selection criteria for RPS grafts. The procurement of RPS grafts [conventional (n = 3) and extended (n = 5)] was performed for 8 of 429 recipients at our center.

Clinical applicability of rapid thrombelastography and functional fibrinogen thrombelastography to adult liver transplantation

Shu Yang Lu, Kenichi A. Tanaka, Ezeldeen Abuelkasem, Raymond M. Planinsic, Tetsuro Sakai – 30 May 2014 – Unlike kaolin thrombelastography (k‐TEG), the clinical utility of rapid thrombelastography (r‐TEG) and functional fibrinogen thrombelastography (FF‐TEG) has not been tested in liver transplantation (LT). These thrombelastography techniques were simultaneously performed at the time of the skin incision (the baseline) and 30 minutes after graft reperfusion (III + 30) for 27 consecutive adult LT patients.

Growth hormone/insulin‐like growth factor 1 dynamics in adult living donor liver transplantation

Maximilian Jara, Antje Schulz, Maciej Malinowski, Gero Puhl, Johan Friso Lock, Daniel Seehofer, Peter Neuhaus, Martin Stockmann – 30 May 2014 – End‐stage liver disease is accompanied by decreased serum levels of insulin‐like growth factor 1 (IGF1) and inversely increased serum levels of growth hormone (GH). Previous reports have demonstrated rapid GH/IGF1 axis recovery after orthotopic liver transplantation.

Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype

Frédéric M. Vaz, Coen C. Paulusma, Hidde Huidekoper, Minke de Ru, Cynthia Lim, Janet Koster, Kam Ho‐Mok, Albert H. Bootsma, Albert K. Groen, Frank G. Schaap, Ronald P. J. Oude Elferink, Hans R. Waterham, Ronald J.A. Wanders – 28 May 2014 – The enterohepatic circulation of bile salts is an important physiological route to recycle bile salts and ensure intestinal absorption of dietary lipids. The Na+‐taurocholate cotransporting polypeptide SLC10A1 (NTCP) plays a key role in this process as the major transporter of conjugated bile salts from the plasma compartment into the hepatocyte.

Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype

Frédéric M. Vaz, Coen C. Paulusma, Hidde Huidekoper, Minke de Ru, Cynthia Lim, Janet Koster, Kam Ho‐Mok, Albert H. Bootsma, Albert K. Groen, Frank G. Schaap, Ronald P. J. Oude Elferink, Hans R. Waterham, Ronald J.A. Wanders – 28 May 2014 – The enterohepatic circulation of bile salts is an important physiological route to recycle bile salts and ensure intestinal absorption of dietary lipids. The Na+‐taurocholate cotransporting polypeptide SLC10A1 (NTCP) plays a key role in this process as the major transporter of conjugated bile salts from the plasma compartment into the hepatocyte.

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