Abstract:
:Immunotherapy of tumours using T cells expanded in vitro has met with mixed clinical success suggesting that a greater understanding of tumour/T-cell interaction is required. We used a HPV16E7 oncoprotein-based mouse tumour model to study this further. In this study, we demonstrate that a HPV16E7 tumour passes through at least three stages of immune susceptibility over time. At the earliest time point, infusion of intravenous immune cells fails to control tumour growth although the same cells given subcutaneously at the tumour site are effective. In a second stage, the tumour becomes resistant to subcutaneous infusion of cells but is now susceptible to both adjuvant activated and HPV16E7-specific immune cells transferred intravenously. In the last phase, the tumour is susceptible to intravenous transfer of HPV16E7-specific cells, but not adjuvant-activated immune cells. The requirement for IFN-gamma and perforin also changes with each stage of tumour development. Our data suggest that effective adoptive T-cell therapy of tumour will need to be matched with the stage of tumour development.
journal_name
Immunol Cell Bioljournal_title
Immunology and cell biologyauthors
Stewart TJ,Fernando GJ,Frazer IH,Leggatt GRdoi
10.1111/j.0818-9641.2004.01273.xsubject
Has Abstractpub_date
2004-10-01 00:00:00pages
455-61issue
5eissn
0818-9641issn
1440-1711pii
ICB1273journal_volume
82pub_type
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journal_title:Immunology and cell biology
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journal_title:Immunology and cell biology
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journal_title:Immunology and cell biology
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journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
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journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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更新日期:1994-10-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.2011.16
更新日期:2012-02-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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更新日期:1992-06-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.2016.53
更新日期:2016-10-01 00:00:00
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journal_title:Immunology and cell biology
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/sj.icb.7100049
更新日期:2007-06-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
doi:10.1046/j.1440-1711.1998.00749.x
更新日期:1998-06-01 00:00:00
abstract::This paper reports the isolation and characterization of sheep umbilical vein endothelial cells (ShUVEC) and examines the kinetics of the expression of intercellular cell adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1). In culture, the cells demonstrate the classical endothelial cell phenot...
journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.1997.4
更新日期:1997-02-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.1993.56
更新日期:1993-12-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.1988.39
更新日期:1988-08-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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更新日期:2005-04-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1038/icb.2016.89
更新日期:2017-02-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
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更新日期:2000-10-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1046/j.1440-1711.2002.01072.x
更新日期:2002-04-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章
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更新日期:1993-02-01 00:00:00
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journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
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更新日期:2001-04-01 00:00:00
abstract::This article attempts to assemble theoretical-teleological argument to explore possible answers to the question of why class I MHC molecules bind smaller peptides than class II MHC molecules and the associated question of why the size of peptides binding to class I molecules is approaching the limit of the self-non-se...
journal_title:Immunology and cell biology
pub_type: 杂志文章,评审
doi:10.1038/icb.1995.15
更新日期:1995-02-01 00:00:00
abstract::Sustained-release vaccine delivery systems may enhance the immunogenicity of subunit vaccines and reduce the need for multiple vaccinations. The aim of this study was to develop a thermoresponsive hydrogel using poloxamer 407-chitosan (CP) grafted copolymer as a delivery system for single-shot sustained-release vaccin...
journal_title:Immunology and cell biology
pub_type: 杂志文章
doi:10.1111/imcb.12031
更新日期:2018-07-01 00:00:00