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3.
Oncologist ; 13(12): 1246-54, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19056856

ABSTRACT

Cancer may occur as a result of abnormal host immune system tolerance. Recent studies have confirmed the occurrence of spontaneous and induced antitumor immune responses expressed as the presence of tumor-infiltrating T cells in the tumor microenvironment in some cancer models. This finding has been recognized as a good prognostic factor in several types of tumors. Some chemotherapy agents, such as anthracyclines and gemcitabine, are effective boosters of the immune response through tumor-specific antigen overexpression after apoptotic tumor cell destruction. Other strategies, such as GM-CSF or interleukin-2, are pursued to increase immune cell availability in the tumor vicinity, and thus improve both antigen presentation and T-cell activation and proliferation. In addition, cytotoxic T lymphocyte antigen 4-blocking monoclonal antibodies enhance immune activity by prolonging T-cell activation. Strategies to stimulate the dormant immune system against tumors are varied and warrant further investigation of their applications to cancer therapy in the future.


Subject(s)
Neoplasms/immunology , Antibodies, Monoclonal/therapeutic use , Antigens, CD/analysis , CTLA-4 Antigen , Granulocyte-Macrophage Colony-Stimulating Factor/therapeutic use , Humans , Immune Tolerance , Lymphocytes, Tumor-Infiltrating/immunology , Neoplasms/drug therapy , Neoplasms/pathology
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