Literature DB >> 28589503

Promise of adeno-associated virus as a gene therapy vector for cardiovascular diseases.

Abesh Bera1, Dwaipayan Sen2.   

Abstract

Cardiovascular diseases pose a unique threat to global mortality because it presents as one of the most diverse conglomerations of pathophysiological conditions that can create significant casualty even without straying into its collateral damage. This puts them right beside obesity and cancer in terms of severity. Their pervasive nature and high prevalence prompted biologists to seek newer prophylactic avenues of addressing this global hazard, among which adeno-associated virus (AAV) gene therapy rose to significant prominence. By virtue of its unrivaled clinical safety quotient, AAVs have been used to rectify various subtypes of cardiovascular ailments, beginning from commonly occurring heart failure to vascular diseases. The review focuses on the history of AAV-mediated gene therapy and contemporary breakthroughs in terms of novel innovations in vector engineering to reduce detargeting, immune response, untimely expression, and so on. We have also focused on the molecular world of cardiomyocytes and endothelial cells but interpreted the therapies in a broader context of cardiovascular pathology. The advances made in each mode of intervention as well as the ones that are beyond the scope of AAV gene therapy or has not been approached through AAV gene therapy as of now have been provided in detail to illustrate the bigger picture of where we stand to combat cardiovascular diseases most efficiently.

Entities:  

Keywords:  AAV therapy; Adeno-associated virus; Cardiovascular disease; Gene therapy; Heart failure; Viral vector

Mesh:

Substances:

Year:  2017        PMID: 28589503     DOI: 10.1007/s10741-017-9622-7

Source DB:  PubMed          Journal:  Heart Fail Rev        ISSN: 1382-4147            Impact factor:   4.214


  246 in total

1.  Mineralocorticoid and AT1 receptors in the paraventricular nucleus contribute to sympathetic hyperactivity and cardiac dysfunction in rats post myocardial infarct.

Authors:  Bing S Huang; Aidong Chen; Monir Ahmad; Hong-Wei Wang; Frans H H Leenen
Journal:  J Physiol       Date:  2014-06-20       Impact factor: 5.182

2.  In vivo gene delivery of HSP70i by adenovirus and adeno-associated virus preserves contractile function in mouse heart following ischemia-reperfusion.

Authors:  Darrell D Belke; Bernd Gloss; John M Hollander; Eric A Swanson; Hervé Duplain; Wolfgang H Dillmann
Journal:  Am J Physiol Heart Circ Physiol       Date:  2006-08-18       Impact factor: 4.733

3.  Cardiac S100A1 protein levels determine contractile performance and propensity toward heart failure after myocardial infarction.

Authors:  Patrick Most; Hanna Seifert; Erhe Gao; Hajime Funakoshi; Mirko Völkers; Jörg Heierhorst; Andrew Remppis; Sven T Pleger; Brent R DeGeorge; Andrea D Eckhart; Arthur M Feldman; Walter J Koch
Journal:  Circulation       Date:  2006-09-04       Impact factor: 29.690

4.  Improved cardiac gene transfer by transcriptional and transductional targeting of adeno-associated viral vectors.

Authors:  Oliver J Müller; Barbara Leuchs; Sven T Pleger; Dirk Grimm; Wolfgang-M Franz; Hugo A Katus; Jürgen A Kleinschmidt
Journal:  Cardiovasc Res       Date:  2006-01-31       Impact factor: 10.787

Review 5.  The war against heart failure: the Lancet lecture.

Authors:  Eugene Braunwald
Journal:  Lancet       Date:  2014-11-16       Impact factor: 79.321

6.  Chronic phospholamban inhibition prevents progressive cardiac dysfunction and pathological remodeling after infarction in rats.

Authors:  Yoshitaka Iwanaga; Masahiko Hoshijima; Yusu Gu; Mitsuo Iwatate; Thomas Dieterle; Yasuhiro Ikeda; Moto-o Date; Jacqueline Chrast; Masunori Matsuzaki; Kirk L Peterson; Kenneth R Chien; John Ross
Journal:  J Clin Invest       Date:  2004-03       Impact factor: 14.808

7.  A novel chimeric adenoassociated virus 2/human bocavirus 1 parvovirus vector efficiently transduces human airway epithelia.

Authors:  Ziying Yan; Nicholas W Keiser; Yi Song; Xuefeng Deng; Fang Cheng; Jianming Qiu; John F Engelhardt
Journal:  Mol Ther       Date:  2013-07-30       Impact factor: 11.454

8.  Altered calcium handling is critically involved in the cardiotoxic effects of chronic beta-adrenergic stimulation.

Authors:  Stefan Engelhardt; Lutz Hein; Vitaly Dyachenkow; Evangelia G Kranias; Gerrit Isenberg; Martin J Lohse
Journal:  Circulation       Date:  2004-02-16       Impact factor: 29.690

9.  Inhibition of miR-25 improves cardiac contractility in the failing heart.

Authors:  Christine Wahlquist; Dongtak Jeong; Agustin Rojas-Muñoz; Changwon Kho; Ahyoung Lee; Shinichi Mitsuyama; Alain van Mil; Woo Jin Park; Joost P G Sluijter; Pieter A F Doevendans; Roger J Hajjar; Mark Mercola
Journal:  Nature       Date:  2014-03-12       Impact factor: 49.962

10.  Calcium upregulation by percutaneous administration of gene therapy in patients with cardiac disease (CUPID 2): a randomised, multinational, double-blind, placebo-controlled, phase 2b trial.

Authors:  Barry Greenberg; Javed Butler; G Michael Felker; Piotr Ponikowski; Adriaan A Voors; Akshay S Desai; Denise Barnard; Alain Bouchard; Brian Jaski; Alexander R Lyon; Janice M Pogoda; Jeffrey J Rudy; Krisztina M Zsebo
Journal:  Lancet       Date:  2016-01-21       Impact factor: 79.321

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  1 in total

Review 1.  Biology of Tissue Inhibitor of Metalloproteinase 3 (TIMP3), and Its Therapeutic Implications in Cardiovascular Pathology.

Authors:  Dong Fan; Zamaneh Kassiri
Journal:  Front Physiol       Date:  2020-06-16       Impact factor: 4.566

  1 in total

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