Results 11 to 20 of about 9,370,992 (242)

Adeno-Associated Virus (AAV) Versus Immune Response [PDF]

open access: yesViruses, 2019
Decades ago, Friedmann and Roblin postulated several barriers to gene therapy, including tissue targeting, delivery across the blood⁻brain barrier (BBB), and host immune responses. These issues remain pertinent till today.
Joseph Rabinowitz   +2 more
doaj   +4 more sources

Human Immune Responses to Adeno-Associated Virus (AAV) Vectors

open access: yesFrontiers in Immunology, 2020
Recombinant adeno-associated virus (rAAV) vectors are one of the most promising in vivo gene delivery tools. Several features make rAAV vectors an ideal platform for gene transfer. However, the high homology with the parental wild-type virus, which often
Giuseppe Ronzitti   +2 more
doaj   +5 more sources

Adeno‐associated virus (AAV)-based gene therapy for glioblastoma [PDF]

open access: yesCancer Cell International, 2021
Glioblastoma (GBM) is the most common and malignant Grade IV primary craniocerebral tumor caused by glial cell carcinogenesis with an extremely poor median survival of 12–18 months.
Xin Xu   +9 more
doaj   +3 more sources

The Interplay between Adeno-Associated Virus and Its Helper Viruses [PDF]

open access: yesViruses, 2020
The adeno-associated virus (AAV) is a small, nonpathogenic parvovirus, which depends on helper factors to replicate. Those helper factors can be provided by coinfecting helper viruses such as adenoviruses, herpesviruses, or papillomaviruses.
Anita F. Meier   +2 more
doaj   +3 more sources

Herpes simplex virus co-infection facilitates rolling circle replication of the adeno-associated virus genome. [PDF]

open access: yesPLoS Pathogens, 2021
Adeno-associated virus (AAV) genome replication only occurs in the presence of a co-infecting helper virus such as adenovirus type 5 (AdV5) or herpes simplex virus type 1 (HSV-1).
Anita Felicitas Meier   +5 more
doaj   +3 more sources

Advances in adeno-associated virus mediated gene therapy in tumors [PDF]

open access: yesJichu yixue yu linchuang, 2021
Adeno-associated virus (AAV) is a human parvovirus with defects and no disease.AAV vector, as an ideal carrier for the transduction of target genes, has certain advantages in long-term gene correction and gene therapy by transferring foreign bases into ...
YANG Xiao-juan, LI Zhen-hao, GOU Yuan-feng, HUO Xia-qin, PEI Ya-ping, LI Na, LIU Hui-ling
doaj   +1 more source

Mass spectrometry friendly pH-gradient anion exchange chromatography for separation of full and empty Adeno-Associated Virus (AAV) capsids [PDF]

open access: yes, 2023
The proportion of full and empty capsids represents a critical quality attribute of adeno-associated virus (AAV)-based therapeutics. In this study, pH-gradient anion exchange chromatography was utilized for the separation of full and empty capsid species.
Florian, Füssl   +3 more
core   +2 more sources

Adeno-Associated Virus (AAV) as a Vector for Gene Therapy [PDF]

open access: yesBioDrugs, 2017
There has been a resurgence in gene therapy efforts that is partly fueled by the identification and understanding of new gene delivery vectors. Adeno-associated virus (AAV) is a non-enveloped virus that can be engineered to deliver DNA to target cells, and has attracted a significant amount of attention in the field, especially in clinical-stage ...
Michael F. Naso   +3 more
openaire   +2 more sources

Adeno-associated virus (AAV) cell entry: structural insights [PDF]

open access: yesTrends in Microbiology, 2022
Adeno-associated virus (AAV) is the leading vector in emerging treatments of inherited diseases. Higher transduction efficiencies and cellular specificity are required for broader clinical application, motivating investigations of virus-host molecular interactions during cell entry.
Nancy L. Meyer, Michael S. Chapman
openaire   +2 more sources

Progress in the use of adeno-associated viral vectors for gene therapy [PDF]

open access: yes, 2004
The development of safe and efficient gene transfer vectors is crucial for the success of gene therapy trials. A viral vector system promising to meet these requirements is based on the apathogenic adeno-associated virus (AAV-2), a member of the ...
Markus Braun-Falco   +7 more
core   +1 more source

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