2000
DOI: 10.1073/pnas.040557897
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Engineered herpes simplex virus expressing IL-12 in the treatment of experimental murine brain tumors

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Cited by 311 publications
(295 citation statements)
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“…While a number of cytokines have been considered for use in anti-tumour therapy (including the use of GM-CSF or IL12 in oncolytic HSV vectors [39][40][41][42][43] ), GM-CSF has generally, and most reliably, given the best results when tested in comparison to other cytokines in pre-clinical models. Clinically, for cancer treatment, indications of efficacy have also been seen when GM-CSF has been delivered by a number of means (eg using engineered, re-injected primary tumour cells -'GVAX'; eg reference 44).…”
Section: Discussionmentioning
confidence: 99%
“…While a number of cytokines have been considered for use in anti-tumour therapy (including the use of GM-CSF or IL12 in oncolytic HSV vectors [39][40][41][42][43] ), GM-CSF has generally, and most reliably, given the best results when tested in comparison to other cytokines in pre-clinical models. Clinically, for cancer treatment, indications of efficacy have also been seen when GM-CSF has been delivered by a number of means (eg using engineered, re-injected primary tumour cells -'GVAX'; eg reference 44).…”
Section: Discussionmentioning
confidence: 99%
“…Thus, delivery of IL-12 by electroporation or viral-based strategies reduced growth of established colon carcinoma, melanoma and brain tumors. [70][71][72][73][74] In the case of breast cancer, the success of IL-12 gene therapy was dependent on the immunogenicity of the tumor. Whereas IL-12 led to regression of highly immunogenic TS/A tumors, the growth of 4T1 tumors, which are considered less immunogenic, was not affected.…”
Section: Therapeutic Effects Of Il-12 In Preclinical Modelsmentioning
confidence: 99%
“…Dans une approche similaire, le gène du symporteur de sodium/iodure (NIS) a été incorporé à plusieurs types de virus oncolytiques. La présence de NIS à la surface [25,26], ainsi qu'à une infiltration accrue de macrophages et de lymphocytes T CD4 + et CD8 + au sein la tumeur [27,28]. De façon intéressante, le gain thérapeutique a pu être amplifié en combinant la surexpression de cytokines à celle de molécules costimulatrices, telles que CD80/B7-1 ou 4-1BBL.…”
Section: Vecteurs D'expression De Gènes Suicideunclassified