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Immune Suppression in Tumors as a Surmountable Obstacle to Clinical Efficacy of Cancer Vaccines

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dc.creator Grégoire Wieërs
dc.creator Nathalie Demotte
dc.creator Danièle Godelaine
dc.creator Pierre Van der Bruggen
dc.date 2011
dc.date.accessioned 2013-05-30T12:06:45Z
dc.date.available 2013-05-30T12:06:45Z
dc.date.issued 2013-05-30
dc.identifier http://www.mdpi.com/2072-6694/3/3/2904/
dc.identifier http://www.doaj.org/doaj?func=openurl&genre=article&issn=20726694&date=2011&volume=3&issue=3&spage=2904
dc.identifier.uri http://koha.mediu.edu.my:8181/jspui/handle/123456789/5009
dc.description Human tumors are usually not spontaneously eliminated by the immune system and therapeutic vaccination of cancer patients with defined antigens is followed by tumor regressions only in a small minority of the patients. The poor vaccination effectiveness could be explained by an immunosuppressive tumor microenvironment. Because T cells that infiltrate tumor metastases have an impaired ability to lyse target cells or to secrete cytokine, many researchers are trying to decipher the underlying immunosuppressive mechanisms. We will review these here, in particular those considered as potential therapeutic targets. A special attention will be given to galectins, a family of carbohydrate binding proteins. These lectins have often been implicated in inflammation and cancer and may be useful targets for the development of new anti-cancer therapies.
dc.language eng
dc.publisher Molecular Diversity Preservation International
dc.source Cancers
dc.subject anergy
dc.subject immunosuppression
dc.subject cancer vaccines
dc.subject galectin
dc.subject tumor-infiltrating lymphocytes
dc.title Immune Suppression in Tumors as a Surmountable Obstacle to Clinical Efficacy of Cancer Vaccines


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