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Updated: May 23, 2026

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Coordinated regulation of myeloid cells by tumours
Dmitry I Gabrilovich1, Suzanne Ostrand-Rosenberg, Vincenzo Bronte
1H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida 33647, USA. dmitry.gabrilovich@ moffitt.org
Abstract:
Myeloid cells are the most abundant nucleated haematopoietic cells in the human body and are a collection of distinct cell populations with many diverse functions. The three groups of terminally differentiated myeloid cells - macrophages, dendritic cells and granulocytes - are essential for the normal function of both the innate and adaptive immune systems. Mounting evidence indicates that the tumour microenvironment alters myeloid cells and can convert them into potent immunosuppressive cells. Here, we consider myeloid cells as an intricately connected, complex, single system and we focus on how tumours manipulate the myeloid system to evade the host immune response.
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