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Myeloid Derived Suppressor Cells in ...

Goulart, Michelle Rodrigues.

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Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications./
作者:	Goulart, Michelle Rodrigues.
面頁冊數:	120 p.
附註:	Source: Dissertation Abstracts International, Volume: 76-01(E), Section: B.
Contained By:	Dissertation Abstracts International76-01B(E).
標題:	Biology, Veterinary Science. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3635149
ISBN:	9781321161212

Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications.
Goulart, Michelle Rodrigues.

Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications. - 120 p.

Source: Dissertation Abstracts International, Volume: 76-01(E), Section: B.

Thesis (Ph.D.)--University of Minnesota, 2014.

Myeloid-derived suppressor cells comprise phenotypically heterogeneous population of myeloid cells at different stages of differentiation endowed with potent immunosuppressive activity. Abnormal accumulation of MDSC in tumor models and cancer patients produce profound immune suppression, severely impairing T cell antitumor immunity, contributing to angiogenesis, cell invasion and metastasis, and constitute a major hurdle in achieving successful immunebased therapies.

ISBN: 9781321161212Subjects--Topical Terms:

1021733
Biology, Veterinary Science.

Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications.
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245 1 0 $a Myeloid Derived Suppressor Cells in Dogs with Cancer: Phenotype, Function and Clinical Implications.
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500 $a Source: Dissertation Abstracts International, Volume: 76-01(E), Section: B.
500 $a Adviser: Elizabeth Pluhar.
502 $a Thesis (Ph.D.)--University of Minnesota, 2014.
520 $a Myeloid-derived suppressor cells comprise phenotypically heterogeneous population of myeloid cells at different stages of differentiation endowed with potent immunosuppressive activity. Abnormal accumulation of MDSC in tumor models and cancer patients produce profound immune suppression, severely impairing T cell antitumor immunity, contributing to angiogenesis, cell invasion and metastasis, and constitute a major hurdle in achieving successful immunebased therapies.
520 $a Understanding the mechanism that drives MDSC expansion and enhances function in humans and dogs is crucial for the development of efficacious immunotherapy.
520 $a Studies in dogs with several tumor types, including sarcoma, carcinomas, mast cell tumors and gliomas confirmed MDSC expansion in the peripheral blood of dog cancer patients. MDSC have been identified in dogs using the combination of three-marker phenotype CD11b+CD14-MHCII -cells for granulocytic and CD11b+CD14+MHCII-cells for monocytic subsets. Granulocytic MDSC accumulated in the peripheral blood of dogs with advanced sarcoma, carcinomas and mast cell tumors, co-purified with peripheral blood mononuclear cell (PBMC) fraction and expressed polymorphic mononuclear morphology. This subset of cells showed the ability to efficiently inhibit T cell proliferation and IFN-gamma secretion of autologous T cells, as well as allogenic T cells from healthy dogs, and expressed ARG1, iNOS2, TGF-beta and IL-10. Monocytic MDSC also demonstrated potent ability to suppress T cell proliferation and preferentially accumulated in the peripheral blood of dogs with glioma. Elevated levels of arginase activity found in the serum of dogs with glioma could potentially be due to the presence of elevated numbers of MDSC. Evaluation of the anti-mouse Gr1 antibody for MDSC staining and identification revealed that does not cross react and therefore is not suitable for canine cells.
590 $a School code: 0130.
650 4 $a Biology, Veterinary Science. $3 1021733
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650 4 $a Health Sciences, Immunology. $3 1017716
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