Click to view Biosketch and Presentation Abstract or page down to review presentation

Similar documents
Drug-Induced Liver Injury and Individual Cell Models

Diagnosis idili other ALI. definite highly likely probable possible unlikely. excluded excluded unlikely probable

Chronic Liver Disease after Acute Hepatocellular DILI

Recent Advances in Hepatotoxicity of Non Steroidal Anti-inflammatory Drugs

Diagnostic evaluation of suspected Drug-Induced Liver Injury

HBV Forum 2 April 18 th 2017 Hilton Amsterdam.

Overview of Causality Assessment in Drug-Induced Liver Injury

DILI: Clinical Pharmacology Considerations for Risk Assessment

Jay H. Hoofnagle, M.D. Director, Liver Disease Research Branch Division of Digestive Diseases and Nutrition National Institute of Diabetes and

Drug-induced liver injury

Leonard B. Seeff, M.D. Consultant Einstein Healthcare Network. Click to view Biosketch and Presentation Abstract or page down to review presentation

Moving from Preclinical to Clinical Studies

Liver injury is a potential complication of many different

Drug-induced liver injury due to varenicline: a case report

Should There Be a Standard of Care (SOC) for Drug-Induced Liver Injury (DILI)? Leonard B Seeff, MD

Non-invasive continuous blood pressure monitoring based on radial artery tonometry (T-Line TL-200pro device) in the intensive care unit

Drug Induced Liver Injury (DILI) Sumita Verma Senior Lecturer Medicine, Hon Consultant Hepatologist Brighton and Sussex Medical School

The Burden of Drug Induced Liver Injury

DRUG-INDUCED LIVER DISEASE THIRD EDITION

Drug Induced Liver Injury at a Tertiary Hospital in India: Etiology, Clinical Features and Predictors of Mortality

Paola Nicoletti, Harshad Devarbhavi, Ashish Goel, CE Eapen, Radha Venkatesan, Jane I Grove, Ann K Daly and Guruprasad P. Aithal

Abstract AIM: To analyze the clinical features of druginduced liver injury (DILI), and discuss the risk factors affecting its prognosis.

Drug induced liver injury: accuracy of diagnosis in published reports

Is there a common mechanism of DILI, do we need to know?

A Severe Hepatotoxicity by Antituberculosis Drug, and its Recovery in Oriental Hospital

Acute Liver Failure in the USA 2011 Evaluation of diagnostic criteria to approach DILI causality

Doc, is it good for my liver?

Drug- induced Liver Injury. Guruprasad P. Aithal

x B versus x ULN for Assessing Drug Effects

The Future Outlook to DILI Research From The Perspective of China

We are updating the design of this site. Try the new test version at Previous Study Return to List Next Study

Drug Induced Liver Injury (DILI)

William M. Lee, MD. Aim: Discuss Clinical Trends in DILI and Acetaminophen Liver Injury

Aim: Discuss Clinical Trends in DILI and Acetaminophen Liver Injury

Positive Rechallenge: What Clinical Trial Data Tell Us Julie Papay, Pharm.D. UCB BioSciences Global Patient Safety

Reliability of causality assessment for drug, herbal and dietary supplement hepatotoxicity in the Drug-Induced Liver Injury Network (DILIN)

A Case of Cold Medicine-Induced Hepatitis Treated with Herbal Medicine

Step Therapy Approval Criteria

DILI PATHOLOGY. PHILIP KAYE November 2017 BSG Pathology Winter Meeting

The Infection Control Doctor and Clostridium difficile infection. Dr David R Jenkins University Hospitals of Leicester NHS Trust, England

Leonard B. Seeff, MD Hepatology Consultant, Retired

ASCT After a Rituximab/Ibrutinib/Ara-c Containing induction in Generalized Mantle Cell Lymphoma

Diagnosis and Management of PBC

Step Therapy Approval Criteria

Case Definition and Phenotype Standardization in Drug-Induced Liver Injury

Yes, the proposed stopping rules are too conservative. John R. Senior, M.D. 25 March 2010 Rethink Stopping Rules 1

HHS Public Access Author manuscript Hepatology. Author manuscript; available in PMC 2017 March 01.

DILI (Hepatotoxicidad)

Chris Bohl, Ph.D. Global Technical Support Manager- Products

ESPEN Congress The Hague 2017

Will Antigen Depletion Restore HBVspecific

Back to Basics: The Basics of Medication Monitoring

Complications of Proton Pump Inhibitor Therapy. Gastroenterology 2017; 153:35-48 발표자 ; F1 김선화

Drug Induced Liver Injury: A Clinical Perspective. Robert J. Fontana, MD

Drug-induced liver injury (DILI)

A Drug-Induced Liver Injury by Western Medication

Intrinsic vs. Idiosyncratic DILI

Toxicology Research REVIEW. Introduction. Rosa Chan and Leslie Z. Benet * View Article Online View Journal

Overview of TCM in Germany

Inhibition of Human Hepatic Bile Acid Transporters as Contributing Factors to Drug-Induced Liver Injury

Primary Results Citation 2

Acute Liver Failure. Neil Shah, MD UNC School of Medicine High-Impact Hepatology Saturday, Dec 8 th, 2018

AAIM: GI Workshop Follow Up to Case Studies. Non-alcoholic Fatty Liver Disease Ulcerative Colitis Crohn s Disease

'The efficacy of extracorporeal liver support with molecular adsorbent recirculating system in severe drug-induced liver injury'.

PREVALENCE OF NAFLD & NASH

Basic patterns of liver damage what information can a liver biopsy provide and what clinical information does the pathologist need?

NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) NON-ALCOHOLIC STEATOHEPATITIS (NASH) ADDRESSING A GROWING SILENT EPIDEMIC

Luminal early breast cancer: (neo-) adjuvant endocrine therapy

Cytochrome P450 interactions

Karen A. Hicks, M.D. Medical Officer Division of Cardiovascular and Renal Products Center for Drug Evaluation and Research, FDA

06 June 2017 DILI Conference XVII FDA/AASLD/Critical Path Institute

Do Histological Features Inform DILI mechanisms?

Blood Transcriptomic Findings in Acute Liver Injury

The first stop for professional medicines advice. Community Pharmacy NSAID Gastro-Intestinal Safety Audit

NON-ALCOHOLIC FATTY LIVER DISEASE (NAFLD) NON-ALCOHOLIC STEATOHEPATITIS (NASH) ADDRESSING A GROWING SILENT EPIDEMIC

AASLD Immune tolerant phase HBV NAFLD diagnostic HCC

Axitinib (renal) Note: in some patients it may be appropriate to increase the dose to 6mg BD before increasing to 7mg BD.

Risk stratification in PBC

Can Study Protocols Protect Patients with Liver Diseases from Serious DILI?

Case Report Metronidazole Induced Liver Injury: A Rare Immune Mediated Drug Reaction

Woman, 35, With Jaundice and Altered Mental Status Lauren Kemph, NP

NONALCOHOLIC FATTY LIVER DISEASE. Non-Alcoholic Fatty Liver Disease (NAFLD) Primary NAFLD. April 13, 2012

Therapies for DILI: NAC, Steroids or NRF-2 activators?

MEDICAL POLICY EFFECTIVE DATE: 12/20/07 REVISED DATE: 12/18/08, 12/17/09, 12/16/10, 12/15/11, 12/20/12, 12/19/13

Suspected drug-induced liver injury associated with iguratimod: a case report and review of the literature

Thrombectomy with the preset stent-retriever. Insights from the ARTESp* trial

COMPOUNDING PHARMACY SOLUTIONS PRESCRIPTION COMPOUNDING FOR PAIN MANAGEMENT

Elucidating Differences in the Hepatotoxic Potential of Tolcapone and Entacapone With DILIsym V R. , a Mechanistic Model of Drug-Induced Liver Injury

Topic review - A patient with impaired liver function. Dr. Karen Hin Kwan Luk 18/1/2018

Non-Alcoholic Fatty Liver Disease

TB Case Management Hepatitis

Drug-, herb- and dietary supplement-induced liver injury

Efficacy and Safety of Seladelpar in Primary Biliary Cholangitis 52-Week Analysis of a Dose-Ranging Phase 2 Study

Table 1 Some of the drugs that induce DILI and the mechanisms underlying their toxicity

Practical Guide to Safety of PPIs What to Tell Your Patient. Proton Pump Inhibitors

Drug therapy in patient with hepatic impairment

ADRs caused by potential. only. Patients (n, %) 132 (49.6%) 111 (41.7%) 10 (3.8%) 2 (0.8%) 9 (3.4%) 2 (0.8%)

SUMMARY INTRODUCTION. Accepted for publication 11 February 2003

Update on HBV Management: Rajesh T. Gandhi, M.D.

Transcription:

Alexander Gerbes, MD Professor of Internal Medicine, Medizinische Klinik und Poliklinik II Klinikum der Universität München, FRG Andreas Benesic, MD Physician, Researcher Medizinische Klinik und Poliklinik II Klinikum der Universität München, FRG Click to view Biosketch and Presentation Abstract or page down to review presentation

CAMPUS GROSSHADERN Transforming monocytes into hepatocyte surrogates A. Benesic and A.L. Gerbes Liver Center Munich - Department of Internal Medicine 2, University Hospital Munich, Germany

CHALLENGES OF IDIOSYNCRATIC DILI (idili) Rare occurence (e.g. 1 in 10.000) Numerous individual factors that influence susceptibility May be difficult to diagnose and especially to identify the causative agent in polymedication Lack of experimental models NEED: Models for idili Positive test supporting the diagnosis and causality assessment 2

MONOCYTE DERIVED HEPATOCYTE-LIKE CELLS (MH CELLS) BACKGROUND Monocytes seem to be important for hepatic repair in models of acute liver injury (1) Monocytes may be capable to transform into hepatocytes(2) Previous data suggest that cells with hepatocyte-like functions can be generated from peripheral monocytes (3, 4) 1) Hogaboam CM, Bone-Larson CL, Steinhauser ML, et al. Am J Pathol. 2000 Apr;156(4):1245-52. 2) Stadtfeld M, Graf T. Development. 2005 Jan;132(1):203-13. Epub 2004 Dec 2. 3) Ruhnke M, Ungefroren H, Nussler A. Gastroenterology. 2005 Jun;128(7):1774-86. 4) Benesic A, Gerbes AL et al. Lab Invest Jun;92(6):926-362; 2012 3

MONOCYTE DERIVED HEPATOCYTE-LIKE CELLS (MH CELLS) GENERATION ISOLATION: 20ml EDTA-plasma Gradient centrifugation Adherence separation of monocytes from EDTA-plasma sample CULTURE: Cultivation in presence of adenosine, IL-3, M-CSF, deoxycholate and caffeine followed by medium containing EGF, FGF4, heparin, glucagon, insulin, deoxycholate and caffeine (1) 4 1) Benesic A, Gerbes AL et al. Lab Invest Jun;92(6):926-362; 2012; US Patent number 8858934

Primary Human Hepatocytes Primary Human Hepatocytes Transforming monocytes into hepatocyte surrogates MONOCYTE DERIVED HEPATOCYTE-LIKE CELLS (MH CELLS) GENE EXPRESSION COMPARED TO HEPATOCYTES Monocytes MH cells R 2 =0,11 R 2 =0,69 Gene expression profiles of monocytes (left) and MH cells (right) compared to primary human hepatocytes (PHH) from the same donor 5

MONOCYTE DERIVED HEPATOCYTE-LIKE CELLS (MH CELLS) DONOR CHARACTERISTICS EXAMPLE: CYP2C9 CYP450 activities and induction levels of primary hepatocytes are reflected by MH cells from the same donor 6

MH CELLS FROM PATIENTS WITH idili CASE: idili BY OMEPRAZOLE =cut off (2xULN) Abbreviations: con: vehicle control positive con: lysis with TWEEN20 APAP: acetaminophen (µm) Diclo: diclofenac (µm) Omep: omeprazole (µm) Panto: pantoprazole (µm) - MH cells of the patient exhibit omeprazole toxicity - No omeprazole toxicity in MH cells of healthy donors nor patients with idili by another drug 7

RESULTS SPECIFICITY OF MH CELL TESTING MH healthy idili diclo idili other than diclo non DILI 2 0 4 0 0 <2 81 0 27 23 MH testing is positive for diclofenac in 4 idili cases with diclofenac as the drug with the highest causality likelihood. No diclofenac toxicity is observed in MH cells derived from healthy donors, idili patients with another drug as cause and non DILI patients, respectively. 8

MH CELLS PILOT STUDY IN PATIENTS WITH ACUTE LIVER INJURY Study aim: Investigation of potential individual toxicity response of MH cells from idili patients in comparison to MH cells from patients with acute liver injury of other origin Methods: Patients treated with at least one drug and acute liver injury according to (1): ALT 5X ULN or AP 2X ULN or ALT 3X ULN and Bili 2X ULN Diagnostic Workup: laboratory testing, imaging, histology (where available), RUCAMscore, drug signature (e.g. LiverTox website (2)) MH cell generation, toxicity testing, data analysis ClinicalTrials.gov Identifier: NCT02353455 1) Aithal GP, Watkins PB, Andrade RJ, Larrey D, Molokhia M, Takikawa H, Hunt CM, Wilke RA, Avigan M, Kaplowitz N, Bjornsson E, Daly AK: Clin Pharmacol Ther. 2011 Jun;89(6):806-15. doi: 10.1038/clpt.2011.58. 2) Hoofnagle JH, Serrano J, Knoben JE, Navarro VJ. Hepatology. 2013 Mar;57(3):873-4. doi: 10.1002/hep.26175 9

DIAGNOSIS OF idili exclusion of other causes drug signature Classification for every drug diagnosis idili non DILI classification: definite highly likely probable possible unlikely other causes of liver injury drug signature definitely excluded typical definitely excluded unlikely probable highly probable atypical OR comedication with compatible signature atypical AND comedication with compatible signature compatible with idili atypical 10

RESULTS: PATIENT CHARACTERISTICS 31 patients with idili and 23 with other causes for acute liver injury idili (n=31) non DILI (n=23) P gender ethnicity pattern 15 female (48%) 16 male (52%) 30 caucasian (97%) 1 hispanic (3%) 22 hepatocellular (71%) 2 mixed (7%) 7 cholestatic (23%) 9 female (39. %) 14 male (61%) n.s. 23 caucasian (100%) n.s. 13 hepatocellular (57%) 0 mixed (0%) 10 cholestatic (43 %) n.s. 11

RESULTS: DRUGS WITH HIGHEST CAUSALITY LIKELIHOOD IN idili 12 Class n drug n NSAID 8 diclofenac 4 metamizol 3 indomethacin 1 ORAL ANTICOAGULANT 4 phenprocoumon 4 ANTITHYROID 2 carbimazole 2 ciprofloxacin 1 ANTI-INFECTIVE 2 piperacillin+ tazobactam 1* IMMUNEMODULATOR 2 ANTIPSYCHOTIC 2 PROTON PUMP INHIBITOR 2 glatirameracetat 1 pembrolizumab 1* olanzapine 1 fluspirilene 1 omeprazole 1 pantoprazole 1 antihistamine 1 cetirizin 1 antifibrotic 1 4-potassium aminobenzoate 1 low-molecular weight heparin 1 enoxaparin 1 phosphodiesterase 5-inhibitor 1 tadalafil 1 serotonin-receptor antagonist 1 sumatriptan 1 oral contraceptive 1 ethinylestradiol + levonorgestrel 1 tyrosin-kinase inhibitor 1 sunitinib 1 vitamin A analogue 1 acitretin 1 muscle relaxant 1 flupirtin 1 *positive rechallenge

RESULTS: DRUG WITH HIGHEST CAUSALITY LIKELIHOOD RUCAM AND MH TOXICITY IN UNEQUIVOCAL CASES - RUCAM 6 is found in 2 non DILI cases - MH testing is negative in 1 case with unequivocal idili 13

RESULTS: DRUG WITH HIGHEST CAUSALITY LIKELIHOOD RUCAM AND MH TOXICITY IN TOTAL STUDY POPULATION * * - RUCAM 6 is found in 29/31 idili cases and 6/23 non DILI cases - MH testing is negative in 2 idili cases, no positive MH testing in non DILI cases *different cases 14

RESULTS: COMEDICATIONS RUCAM AND MH TOXICITY IN TOTAL STUDY POPULATION Test results for comedications in all idili (n=31) and non DILI (n=23) cases (up to 4 drugs per patient): - RUCAM is 6 for 27/53 comedications in idili cases and 2/39 non DILI cases - MH testing is positive for 4 comedications in idili cases, no positive results in non DILI cases 15

RESULTS: ALL DRUGS IN TOTAL POPULATION TEST RESULTS COMPARED TO CAUSALITY LIKELIHOOD - RUCAM yields a relevant proportion of false results for drugs with intermediate causality likelihood - MH testing shows stable results independent on causality likelihood 16

SUMMARY Our data suggest that monocytes can aquire some hepatocyte properties in vitro and seem to reflect donor specific characteristics In this pilot study toxicity was higher in MH cells derived from idili patients compared to patients with non DILI acute liver injury or healthy donors MH cells offer the possibility to assist with diagnosis of idili and causality assessment OUTLOOK Ongoing research further characterises the model using Omics-technologies Further data are needed from patients who tolerate potential idili drugs 17