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Pregled bibliografske jedinice broj: 890724

Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome


Bortolussi, Giulia; Zentillin, Lorena; Vaníkova, Jana; Bočkor, Luka; Bellarosa, Cristina; Mancarella, Antonio; Vianello, Eleonora; Tiribelli, Claudio; Giacca, Mauro; Vitek, Libor; Muro Andrés F.
Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome // Human gene therapy, 25 (2014), 9; 844-855 doi:10.1089/hum.2013.233 (međunarodna recenzija, članak, znanstveni)


CROSBI ID: 890724 Za ispravke kontaktirajte CROSBI podršku putem web obrasca

Naslov
Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome

Autori
Bortolussi, Giulia ; Zentillin, Lorena ; Vaníkova, Jana ; Bočkor, Luka ; Bellarosa, Cristina ; Mancarella, Antonio ; Vianello, Eleonora ; Tiribelli, Claudio ; Giacca, Mauro ; Vitek, Libor ; Muro Andrés F.

Izvornik
Human gene therapy (1043-0342) 25 (2014), 9; 844-855

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Crigler–Najjar syndrome type I, hyperbilirubinemia, gene therapy, AAV

Sažetak
Null mutations in the UGT1A1 gene result in Crigler–Najjar syndrome type I (CNSI), characterized by severe hyperbilirubinemia and constant risk of developing neurological damage. Phototherapy treatment lowers plasma bilirubin levels, but its efficacy is limited and liver transplantation is required. To find alternative therapies, we applied AAV liver- specific gene therapy to a lethal mouse model of CNSI. We demonstrated that a single neonatal hUGT1A1 gene transfer was successful and the therapeutic effect lasted up to 17 months postinjection. The therapeutic effect was mediated by the presence of transcriptionally active double-stranded episomes. We also compared the efficacy of two different gene therapy approaches: liver versus skeletal muscle transgene expression. We observed that 5–8% of normal liver expression and activity levels were sufficient to significantly reduce bilirubin levels and maintain lifelong low plasma bilirubin concentration (3.1±1.5 mg/dl). In contrast, skeletal muscle was not able to efficiently lower bilirubin (6.4±2.0 mg/dl), despite 20–30% of hUgt1a1 expression levels, compared with normal liver. We propose that this remarkable difference in gene therapy efficacy could be related to the absence of the Mrp2 and Mrp3 transporters of conjugated bilirubin in muscle. Taken together, our data support the concept that liver is the best organ for efficient and long-term CNSI gene therapy, and suggest that the use of extra- hepatic tissues should be coupled to the presence of bilirubin transporters.

Izvorni jezik
Engleski

Znanstvena područja
Biologija, Kliničke medicinske znanosti, Biotehnologija



POVEZANOST RADA


Profili:

Avatar Url Luka Bočkor (autor)

Poveznice na cjeloviti tekst rada:

doi online.liebertpub.com doi.org

Citiraj ovu publikaciju:

Bortolussi, Giulia; Zentillin, Lorena; Vaníkova, Jana; Bočkor, Luka; Bellarosa, Cristina; Mancarella, Antonio; Vianello, Eleonora; Tiribelli, Claudio; Giacca, Mauro; Vitek, Libor; Muro Andrés F.
Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome // Human gene therapy, 25 (2014), 9; 844-855 doi:10.1089/hum.2013.233 (međunarodna recenzija, članak, znanstveni)
Bortolussi, G., Zentillin, L., Vaníkova, J., Bočkor, L., Bellarosa, C., Mancarella, A., Vianello, E., Tiribelli, C., Giacca, M., Vitek, L. & Muro Andrés F. (2014) Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome. Human gene therapy, 25 (9), 844-855 doi:10.1089/hum.2013.233.
@article{article, author = {Bortolussi, Giulia and Zentillin, Lorena and Van\'{\i}kova, Jana and Bo\v{c}kor, Luka and Bellarosa, Cristina and Mancarella, Antonio and Vianello, Eleonora and Tiribelli, Claudio and Giacca, Mauro and Vitek, Libor}, year = {2014}, pages = {844-855}, DOI = {10.1089/hum.2013.233}, keywords = {Crigler–Najjar syndrome type I, hyperbilirubinemia, gene therapy, AAV}, journal = {Human gene therapy}, doi = {10.1089/hum.2013.233}, volume = {25}, number = {9}, issn = {1043-0342}, title = {Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome}, keyword = {Crigler–Najjar syndrome type I, hyperbilirubinemia, gene therapy, AAV} }
@article{article, author = {Bortolussi, Giulia and Zentillin, Lorena and Van\'{\i}kova, Jana and Bo\v{c}kor, Luka and Bellarosa, Cristina and Mancarella, Antonio and Vianello, Eleonora and Tiribelli, Claudio and Giacca, Mauro and Vitek, Libor}, year = {2014}, pages = {844-855}, DOI = {10.1089/hum.2013.233}, keywords = {Crigler–Najjar syndrome type I, hyperbilirubinemia, gene therapy, AAV}, journal = {Human gene therapy}, doi = {10.1089/hum.2013.233}, volume = {25}, number = {9}, issn = {1043-0342}, title = {Life-Long Correction of Hyperbilirubinemia with a Neonatal Liver-Specific AAV-Mediated Gene Transfer in a Lethal Mouse Model of Crigler–Najjar Syndrome}, keyword = {Crigler–Najjar syndrome type I, hyperbilirubinemia, gene therapy, AAV} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE


Uključenost u ostale bibliografske baze podataka::


  • BIOSIS Previews (Biological Abstracts)
  • CA Search (Chemical Abstracts)
  • EMBASE (Excerpta Medica)
  • MEDLINE
  • Biotechnology Citation Index
  • Derwent Drug File
  • EMBiology
  • Journal Citation Reports/Science Edition
  • ProQuest databases


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