Literature DB >> 22856608

Adeno-associated virus vectors: immunobiology and potential use for immune modulation.

Grant J Logan1, Ian E Alexander.   

Abstract

Recombinant viral vectors based on the human parvovirus, adeno-associated virus (AAV) show considerable promise for human therapeutic application. An important feature that sets this gene transfer system apart from other contemporary virus-based systems is relatively weak induction of innate and cognate immune responses, such that in defined contexts foreign antigens can be expressed long-term in immune competent hosts. This in turn has led to increasing interest in the possibility of exploiting AAV for immune system modulation, including both the induction and avoidance of antigen- specific responses, depending on the therapeutic need. This interest is fuelled by the recognition that the full potential of cell and gene based therapies cannot be realised without parallel developments in therapeutic immune system modulation that allow specific rather than generalised immunosuppression. This review outlines current understanding of AAV immunobiology and explores its potential as a tool for therapeutic manipulation of immune system responses.

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Year:  2012        PMID: 22856608     DOI: 10.2174/156652312802083639

Source DB:  PubMed          Journal:  Curr Gene Ther        ISSN: 1566-5232            Impact factor:   4.391


  6 in total

1.  AAV-mediated targeting of gene expression to the peri-infarct region in rat cortical stroke model.

Authors:  Kert Mätlik; Usama Abo-Ramadan; Brandon K Harvey; Urmas Arumäe; Mikko Airavaara
Journal:  J Neurosci Methods       Date:  2014-08-23       Impact factor: 2.390

2.  Inactivation of the human papillomavirus E6 or E7 gene in cervical carcinoma cells by using a bacterial CRISPR/Cas RNA-guided endonuclease.

Authors:  Edward M Kennedy; Anand V R Kornepati; Michael Goldstein; Hal P Bogerd; Brigid C Poling; Adam W Whisnant; Michael B Kastan; Bryan R Cullen
Journal:  J Virol       Date:  2014-08-06       Impact factor: 5.103

3.  Serotype-specific Binding Properties and Nanoparticle Characteristics Contribute to the Immunogenicity of rAAV1 Vectors.

Authors:  Maxime Ferrand; Sylvie Da Rocha; Guillaume Corre; Anne Galy; Florence Boisgerault
Journal:  Mol Ther       Date:  2015-04-16       Impact factor: 11.454

4.  Antiproliferative effects of AAV-delivered CRISPR/Cas9-based degradation of the HPV18-E6 gene in HeLa cells.

Authors:  Zahra Noroozi; Mehdi Shamsara; Elahe Valipour; Sahar Esfandyari; Alireza Ehghaghi; Amir Monfaredan; Zahra Azizi; Elahe Motevaseli; Mohammad Hossein Modarressi
Journal:  Sci Rep       Date:  2022-02-09       Impact factor: 4.379

5.  Gene transfer of mutant mouse cholinesterase provides high lifetime expression and reduced cocaine responses with no evident toxicity.

Authors:  Liyi Geng; Yang Gao; Xiabin Chen; Shurong Hou; Chang-Guo Zhan; Zoran Radic; Robin J Parks; Stephen J Russell; Linh Pham; Stephen Brimijoin
Journal:  PLoS One       Date:  2013-06-28       Impact factor: 3.240

6.  Production of adeno-associated virus (AAV) serotypes by transient transfection of HEK293 cell suspension cultures for gene delivery.

Authors:  Parminder Singh Chahal; Erica Schulze; Rosa Tran; Johnny Montes; Amine A Kamen
Journal:  J Virol Methods       Date:  2013-11-13       Impact factor: 2.014

  6 in total

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