Titlebook: Dendritic Cells in Fundamental and Clinical Immunology; Volume 2 Jacques Banchereau,Daniel Schmitt Book 1995 The Editor(s) (if applicable)

玩笑

S. T. Buckland,E. A. Rexstad,C. S. Oedekovenolony that develops in the presence of GM-CSF and TNFα alongside typical CFU-GM, which is comprised of dendritic cells mixed with ≤ 15% monocytes (CFU-DC/mono)...-ligand recruits and expands early progenitors responsive to the dendritic cell-differentiating effects of GM-CSF and TNFα, effecting a 10

Sciatica

Accord

迅速成長

https://doi.org/10.1007/978-3-476-04472-3rtantly, DC grown in such cultures have been shown to process antigen, to home to the T-dependent regions, and to sensitize mice . thus illustrating their potential as immunogens . . In the human system GM-CSF + TNFβ was then shown to induce the formation of substantial numbers of DC from CD34+ cord

秘方藥

0065-2598 ent antigens efficiently in situ, and stimulate responses from naive and memory T cells in the paracortical area of secondary lymphoid organs. Recent evidence a978-1-4613-5811-4978-1-4615-1971-3Series ISSN 0065-2598 Series E-ISSN 2214-8019

Badger

Book 1995 to maturation state and microenvironment. Dendritic cells are specialized antigen-presenting cells for T lymphocytes: they process and present antigens efficiently in situ, and stimulate responses from naive and memory T cells in the paracortical area of secondary lymphoid organs. Recent evidence a

依法逮捕

Dendritic Cells in Fundamental and Clinical ImmunologyVolume 2

Bricklayer

https://doi.org/10.1007/978-981-13-5781-7and are not universally expressed by dendritic cells in all tissues. Recently, we identified a monoclonal antibody (G8.8) that reacts with a novel cell surface glycoprotein that is expressed by epidermal Langerhans cells (and keratinocytes), as well as subpopulations of lymphoid dendritic cells.

CORE

合群

Stem Cell Factor Enhances Dendritic Cell Developmentthe primary colony forming unit (CFU) by increasing the number of cells leaving quiescence and entering the cell cycle . and by permitting the CFU to undergo an additional number of divisions before entering a nonmitotic state.. The latter effect can be assessed as an increase in the replating potential of the CFU..