The Immune System in the Pathogenesis of Ovarian Cancer

被引:54
作者
Charbonneau, Bridget [1 ]
Goode, Ellen L. [1 ]
Kalli, Kimberly R. [2 ]
Knutson, Keith L. [3 ]
DeRycke, Melissa S. [1 ]
机构
[1] Mayo Clin, Dept Hlth Sci Res, Rochester, MN 55905 USA
[2] Mayo Clin, Div Oncol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Immunol, Rochester, MN 55905 USA
关键词
cytokines; T cells; macrophages; single nucleotide polymorphisms; dendritic cells; REGULATORY T-CELLS; TUMOR-NECROSIS-FACTOR; ANTI-INTERLEUKIN-6; MONOCLONAL-ANTIBODY; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PELVIC-INFLAMMATORY-DISEASE; SERUM INTERLEUKIN-6 LEVELS; GENOME-WIDE ASSOCIATION; SILTUXIMAB CNTO 328; INDOLEAMINE 2,3-DIOXYGENASE; DENDRITIC CELLS;
D O I
10.1615/CritRevImmunol.2013006813
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Clinical outcomes in ovarian cancer are heterogeneous even when considering common features such as stage, response to therapy, and grade. This disparity in outcomes warrants further exploration into tumor and host characteristics. One compelling host characteristic is the immune response to ovarian cancer. While several studies have confirmed a prominent role for the immune system in modifying the clinical course of the disease, recent genetic and protein analyses also suggest a role in disease incidence. Recent studies also show that anti-tumor immunity is often negated by immune suppressive cells present in the tumor microenvironment. These suppressive immune cells also directly enhance the pathogenesis through the release of various cytokines and chemokines, which together form an integrated pathologic network. Thus, future research into immunotherapy targeting ovarian cancer will likely become increasingly focused on combination approaches that simultaneously augment immunity while preventing local immune suppression or by disrupting critical cytokine networks.
引用
收藏
页码:137 / 164
页数:28
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