Literature DB >> 22353155

Biopump: Autologous skin-derived micro-organ genetically engineered to provide sustained continuous secretion of therapeutic proteins.

Eduardo Mitrani1, Andrew Pearlman, Baruch Stern, Reem Miari, Haim Goltsman, Nikolai Kunicher, Amos Panet.   

Abstract

A novel approach for sustained production of therapeutic proteins is described, using genetic modification of intact autologous micro-organ tissue explants from the subject's own skin. The skin-derived micro-organ can be maintained viable ex vivo for extended periods and is transduced with a transgene encoding a desired therapeutic protein, resulting in protein-secreting micro-organ (biopump (BP)). The daily protein production from each BP is quantified, enabling drug dosing by subcutaneous implantation of the requisite number of BPs into the patient to provide continuous production to the circulation of a known amount of the therapeutic protein. Each implanted BP remains localized and is accessible, to enable removal or ablation if needed. Examples from preclinical and clinical studies are presented, including use of associated virus vector 1 and helper-dependent adenoviral vectors producing BPs to provide long-term sustained secretion of recombinant interferon-α and erythropoietin.
© 2012 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22353155     DOI: 10.1111/j.1529-8019.2012.01457.x

Source DB:  PubMed          Journal:  Dermatol Ther        ISSN: 1396-0296            Impact factor:   2.851


  3 in total

Review 1.  Challenges and Prospects for Helper-Dependent Adenoviral Vector-Mediated Gene Therapy.

Authors:  Pasquale Piccolo; Nicola Brunetti-Pierri
Journal:  Biomedicines       Date:  2014-04-02

2.  One-Vector System for Multiplexed CRISPR/Cas9 against Hepatitis B Virus cccDNA Utilizing High-Capacity Adenoviral Vectors.

Authors:  Maren Schiwon; Eric Ehrke-Schulz; Andreas Oswald; Thorsten Bergmann; Thomas Michler; Ulrike Protzer; Anja Ehrhardt
Journal:  Mol Ther Nucleic Acids       Date:  2018-06-07       Impact factor: 8.886

3.  Integrating HDAd5/35++ Vectors as a New Platform for HSC Gene Therapy of Hemoglobinopathies.

Authors:  Chang Li; Nikoletta Psatha; Hongjie Wang; Manvendra Singh; Himanshu Bhusan Samal; Wenli Zhang; Anja Ehrhardt; Zsuzsanna Izsvák; Thalia Papayannopoulou; André Lieber
Journal:  Mol Ther Methods Clin Dev       Date:  2018-02-15       Impact factor: 6.698

  3 in total

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