These results also suggest that additional clinical development PR-171 nmr of eluxadoline is warranted to validate the clinical meaningfulness of the composite end point and to determine what baseline patient characteristics are predictive of clinical response with eluxadoline. “
“Patients chronically infected with hepatitis B virus (HBV) are at high risk for developing cirrhosis and hepatocellular carcinoma (HCC), which lead to more than 0.5 million deaths per year.1 Antiviral nucleos(t)ide analogues control but do not eradicate the virus because they do not target the

nuclear persistence form of the virus, the covalently closed circular DNA (cccDNA).2 The episomal HBV cccDNA serves as a transcription template and can cause a relapse of hepatitis B when pharmacological treatment ends.3 and 4 During acute, self-limited hepatitis B, patients mount a strong T-cell response against multiple viral antigens5, 6, 7 and 8 that is required to eliminate check details cccDNA-positive hepatocytes and to clear the virus.9 Such a T-cell response is lacking in chronic infection. The aim of immunotherapy against chronic

hepatitis B is to restore efficient antiviral immune responses and complement pharmacological antiviral therapy to eliminate remaining infected cells. A promising immunotherapeutic approach is the adoptive transfer of genetically modified HBV-specific T cells. In infected cells, HBV envelope proteins are incorporated into endoplasmic

reticulum membranes, where they either form (sub)viral particles or may reach the cell surface by physiological membrane exchange.10 These (sub)viral particles can be detected in large amounts in sera of infected patients as hepatitis B surface antigen (HBsAg) and very likely contribute to induction of immune tolerance.11 Because the expression of HBV surface proteins is not controlled by available antiviral agents and is usually maintained in HCC with integrated viral genomes, HBsAg remains positive under antiviral therapy, Vildagliptin even in late stages of chronic hepatitis B in which HCC has developed. Targeting HBV surface proteins therefore seems most promising. We have previously shown that expression of a chimeric antigen receptor (CAR) directed against the HBV surface proteins enables human T cells to kill HBV-infected human hepatocytes and to eliminate viral cccDNA in vitro.12 On this basis, we here addressed the question whether CAR-grafted, adoptively transferred T cells would retain their function in vivo and control virus replication without significant T cell–related toxicity in a model of persistent HBV infection in HBV transgenic (HBVtg) mice with a functional immune system. C57BL/6 (CD45.1+) and HBVtg HBV1.3xfs mice (HBV genotype D, serotype ayw 13, CD45.2+) were bred in specific pathogen–free animal facilities.