The terminology issue for myeloid-derived suppressor cells.

By Dmitry I. Gabrilovich, Vincenzo Bronte, Shu-hsia Chen, M. P. Colombo, Augusto C Ochoa, S. Ostrand-Rosenberg, Hans Schreiber. Cancer Research, 2007

809 citations recorded by the source corpus.

Subfields: Immunology

View Paper: https://www.semanticscholar.org/paper/a0b80f3f86a06dd81b074cafda9190b6a463414e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Immunology

Citations in the corpus

Arginine regulation by myeloid derived suppressor cells and tolerance in cancer: mechanisms and therapeutic perspectives (2008, background): “Recently, a panel of leading investigators in the field agreed to use the common term ‘myeloid derived suppressor cells’ (MDSCs) to name these arginase I-producing cells (99).”
Tumor‐induced tolerance and immune suppression by myeloid derived suppressor cells (2008, positive): “The acronym MDSCs, which reflects the myeloid origin (thus including both mature and immature/precursor phenotypes) and the immunosuppressive functions (18), was recently accepted by some investigators to replace the previous terms of ‘myeloid suppressor cells (MSCs)’ or ‘immature myeloid cells (iMC”
Adipose Tissue in Obesity-Related Inflammation and Insulin Resistance: Cells, Cytokines, and Chemokines (2013, neutral): “Later on, these cells were defined as “myeloid-derived suppressor cells” (MDSC) because of their myeloid origin and their ability to suppress immune responses [106].”
IL-6 in inflammation, autoimmunity and cancer (2020, background): “The requirement for human naive T cells in T h 17 cell differentiation differs from that of mice, since human T cells in the presence of IL-1 β with IL-6 or IL-23 can differentiate to T h 17 cells without TGF β (169, 170).”
Tumor‐associated macrophages (TAM) as major players of the cancer‐related inflammation (2009, background): “However, as these cells share properties and gene expression profiles with M2-polarized TAM [34, 61] it is likely that, by nature, they skew toward the M2 orientation.”
Microenvironmental regulation of metastasis (2009, background): “Another BMDC type, which may share a common progenitor with TAMs, is the MDS”
Tumor-derived granulocyte-macrophage colony stimulating factor regulates myeloid inflammation and T cell immunity in pancreatic cancer (2012, methodology): “Furthermore, normal pancreatic ductal cells also secreted VEGF (albeit somewhat less so than PDA cells) yet Gr-1 + CD11b + cells did not accumulate around normal ducts in vivo and conditioned media from normal ductal cells failed to support proliferation of c-kit + splenocytes into MDSC.”
The role of myeloid cells in the promotion of tumour angiogenesis (2008, background): “Indeed, it is their ability to potently suppress the anti-tumour functions of T and natural killer (NK) cells, along with DC maturation, that currently provides the most effective way of identifying MDS”
Visualizing stromal cell dynamics in different tumor microenvironments by spinning disk confocal microscopy (2008, positive): “In addition, 13% co-expressed CD11b and Gr1 (Ly-6G), a marker for neutrophils and MDSCs (Mordue and Sibley, 2003; Gabrilovich et al., 2007) (Fig.”
Cancer to bone: a fatal attraction (2011, neutral): “Myeloid-derived suppressor cells (MDSCs) are a subpopulation of immature myeloid cells that are characterized by GR1 expression and by the αMβ2 (CD11b) integrin adhesion marke”