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dc.contributor.authorKhetani, Salman R.
dc.contributor.authorTrehan, Kartik
dc.contributor.authorPloss, Alexander
dc.contributor.authorJones, Christopher T.
dc.contributor.authorSyder, Andrew J.
dc.contributor.authorGaysinskaya, Valeriya A.
dc.contributor.authorMu, Kathy
dc.contributor.authorRitola, Kimberly
dc.contributor.authorRice, Charles M.
dc.contributor.authorBhatia, Sangeeta N
dc.date.accessioned2014-04-11T16:00:02Z
dc.date.available2014-04-11T16:00:02Z
dc.date.issued2010-02
dc.date.submitted2209-12
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/86110
dc.description.abstractHepatitis C virus (HCV) remains a major public health problem, affecting approximately 130 million people worldwide. HCV infection can lead to cirrhosis, hepatocellular carcinoma, and end-stage liver disease, as well as extrahepatic complications such as cryoglobulinemia and lymphoma. Preventative and therapeutic options are severely limited; there is no HCV vaccine available, and nonspecific, IFN-based treatments are frequently ineffective. Development of targeted antivirals has been hampered by the lack of robust HCV cell culture systems that reliably predict human responses. Here, we show the entire HCV life cycle recapitulated in micropatterned cocultures (MPCCs) of primary human hepatocytes and supportive stroma in a multiwell format. MPCCs form polarized cell layers expressing all known HCV entry factors and sustain viral replication for several weeks. When coupled with highly sensitive fluorescence- and luminescence-based reporter systems, MPCCs have potential as a high-throughput platform for simultaneous assessment of in vitro efficacy and toxicity profiles of anti-HCV therapeutics.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 DK56966)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH Roadmap for Medical Research Grant 1 R01 DK085713-01)en_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.0915130107en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePNASen_US
dc.titlePersistent hepatitis C virus infection in microscale primary human hepatocyte culturesen_US
dc.typeArticleen_US
dc.identifier.citationPloss, A., S. R. Khetani, C. T. Jones, A. J. Syder, K. Trehan, V. A. Gaysinskaya, K. Mu, K. Ritola, C. M. Rice, and S. N. Bhatia. “Persistent Hepatitis C Virus Infection in Microscale Primary Human Hepatocyte Cultures.” Proceedings of the National Academy of Sciences 107, no. 7 (February 16, 2010): 3141–3145.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.mitauthorKhetani, Salman R.en_US
dc.contributor.mitauthorTrehan, Kartiken_US
dc.contributor.mitauthorBhatia, Sangeeta N.en_US
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsPloss, A.; Khetani, S. R.; Jones, C. T.; Syder, A. J.; Trehan, K.; Gaysinskaya, V. A.; Mu, K.; Ritola, K.; Rice, C. M.; Bhatia, S. N.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1293-2097
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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