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Myeloid Cell Mediated Immune Suppression in Pancreatic Cancer.
Kemp, Samantha B; Pasca di Magliano, Marina; Crawford, Howard C.
Afiliación
  • Kemp SB; Department of Molecular and Cellular Pathology, Ann Arbor, Michigan.
  • Pasca di Magliano M; Department of Surgery, Ann Arbor, Michigan; Department of Cell and Developmental Biology; Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan. Electronic address: marinapa@umich.edu.
  • Crawford HC; Henry Ford Pancreatic Cancer Center, Henry Ford Health System, Detroit, Michigan. Electronic address: hcrawfo1@hfhs.org.
Cell Mol Gastroenterol Hepatol ; 12(5): 1531-1542, 2021.
Article en En | MEDLINE | ID: mdl-34303882
Pancreatic ductal adenocarcinoma (PDA), the most common pancreatic cancer, is a nearly universally lethal malignancy. PDA is characterized by extensive infiltration of immunosuppressive myeloid cells, including tumor-associated macrophages and myeloid-derived suppressor cells. Myeloid cells in the tumor microenvironment inhibit cytotoxic T-cell responses promoting carcinogenesis. Immune checkpoint therapy has not been effective in PDA, most likely because of this robust immune suppression, making it critical to elucidate mechanisms behind this phenomenon. Here, we review myeloid cell infiltration and cellular crosstalk in PDA progression and highlight current therapeutic approaches to target myeloid cell-driven immune suppression.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Células Mieloides / Inmunomodulación / Microambiente Tumoral Límite: Animals / Humans Idioma: En Revista: Cell Mol Gastroenterol Hepatol Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Pancreáticas / Células Mieloides / Inmunomodulación / Microambiente Tumoral Límite: Animals / Humans Idioma: En Revista: Cell Mol Gastroenterol Hepatol Año: 2021 Tipo del documento: Article
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