The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Immune Responses to Lentiviral Vectors
Abstract
Efficient delivery and sustained expression of a therapeutic gene into human tissues are the requisite to accomplish the high expectations of gene therapy. A major challenge has concerned development of gene transfer systems capable of efficient cell transduction and transgene expression without harm to the recipient. A lot of work has been done to demonstrate the efficacy of gene therapy in animal models that mimic situations in humans. Use of lentiviral vectors (LVs) offers multiple advantages for gene replacement therapy, because they combine efficient delivery, ability to transduce proliferating and resting cells, capacity to integrate into the host chromatin to provide stable long-term expression of the transgene, absence of any viral genes in the vector and absence of interference from preexisting viral immunity. However, one of the major barriers to stable gene transfer by LVs and other viral vectors is the development of innate and adaptive immune responses to the delivery vector and the transferred therapeutic transgene. Since this greatly hinders the therapeutical benefits of gene therapy by LVs, developing strategies to overcome the host immune response to the transfer vector and the transgene is a matter of current investigation.
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Typical AdVs and LVs elicit strong immune responses.
“typical AdVs and LVs elicit strong immune responses (Follenzi et al., 2007; Ahi et al., 2011).”
From Delivering CRISPR: a review of the challenges and approaches (2018) · cites this paper as Follenzi et al., 2007
Citations
Cites
In Vivo Gene Delivery and Stable Transduction of Nondividing Cells by a Lentiviral Vector
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A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency
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Therapeutic targeting of innate immunity with Toll-like receptor agonists and antagonists
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Cd8(+) T-Cell Responses to Adeno-Associated Virus Capsid in Humans
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Induction of Immune Tolerance to Coagulation Factor IX Antigen by In Vivo Hepatic Gene Transfer
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Induction of antigen-specific CD4+ T-cell anergy and deletion by in vivo viral gene transfer
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CD4+ CD25+ regulatory T cells inhibit immune-mediated transgene rejection
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Delivering CRISPR: a review of the challenges and approaches
Lino, C. A., Harper, J. C., Carney, J. P., & Timlin, J. A. (2018) · Drug Delivery · doi:10.1080/10717544.2018.1474964 · Cited by 1,185
The Non-Obese Diabetic (NOD) Mouse as a Model of Human Type 1 Diabetes
Kachapati, K., Adams, D., Bednar, K., & Ridgway, W. M. (2012) · Methods in Molecular Biology · doi:10.1007/978-1-62703-068-7_1 · Cited by 54
Metadata
- Authors
- Follenzi, A., Santambrogio, L., & Annoni, A.
- Venue
- Current Gene Therapy
- Publisher
- Bentham Science Publishers Ltd.
- Published
- 2007-10-01
- Volume
- 7
- Issue
- 5
- Pages
- 306-315
- ISSN
- 1566-5232
- Cited by
- 87
- References
- 12
- Language
- en
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