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Immunological Evasion in Glioblastoma

期刊

BIOMED RESEARCH INTERNATIONAL
卷 2016, 期 -, 页码 -

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HINDAWI LTD
DOI: 10.1155/2016/7487313

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资金

  1. National Council of Science and Technology of Mexico (CONACyT) from Doctor Benjamin Pineda [CB-180851]
  2. CONACyT from Doctor Sergio Moreno [FOSSIS-182362]
  3. National Institute of Neurology and Neurosurgery (Research Department)
  4. CONACyT [53351]

向作者/读者索取更多资源

Glioblastoma is the most aggressive tumor in Central Nervous System in adults. Among its features, modulation of immune system stands out. Although immune system is capable of detecting and eliminating tumor cells mainly by cytotoxic T and NK cells, tumor microenvironment suppresses an effective response through recruitment of modulator cells such as regulatory T cells, monocyte-derived suppressor cells, M2 macrophages, and microglia as well as secretion of immunomodulators including IL-6, IL-10, CSF-1, TGF-beta, and CCL2. Other mechanisms that induce immunosuppression include enzymes as indolamine 2,3-dioxygenase. For this reason it is important to develop new therapies that avoid this immune evasion to promote an effective response against glioblastoma.

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