The role of chemokine receptors in primary, effector, and memory immune responses.
By F. Sallusto, C. Mackay, A. Lanzavecchia. Annual Review of Immunology, 2000
1,200 citations recorded by the source corpus.
Subfields: Immunology, Oncology
View Paper: https://www.semanticscholar.org/paper/7580a70b7d7b5ca72bd2605cab6260cc2961f25e
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Citations in the corpus
- The transcriptional repressor Bcl-6 directs T follicular helper cell lineage commitment. (2009, background): “…cytokines to provide protection from various types of pathogenic challenge (Ho and Glimcher, 2002; Murphy and Reiner, 2002; Reiner, 2007; Weaver et al., 2007) and expressing diverse chemokine receptors for homing to different tissue microenvironments (Bromley et al., 2008; Sallusto et al., 2000).”
- The multifaceted role of CD4+ T cells in the regulation of CD8+ T cell memory maturation (2015, neutral): “Nevertheless, expression of CD45 isoforms together with chemokine receptors and selectins is now widely used to distinguish naive and memory T cells in humans 64 .”
- Understanding dendritic cell and T‐lymphocyte traffic through the analysis of chemokine receptor expression (2000, background): “Total CD8 T cells were stained with CD45RA and CCR7 to identify naïve (1), TCM (2) and TEM (3 & 4).”
- Chemokines as regulators of T cell differentiation (2001, background): “Homing of effector T cells to sites of inflammation is also dependent on chemokine”
- Chemokines: immunology's high impact factors (2001, neutral): “In the periphery, chemokine receptors are regulated markedly after naive T cell activation, effector T cell differentiation and memory cell developmen”
- Kinetics of dendritic cell activation: impact on priming of TH1, TH2 and nonpolarized T cells (2000, background): “gif" NDATA ITEM> ]> T helper type 1 (T H 1) and type 2 (T H 2) cells represent terminally differentiated effector cells characterized by different cytokine production and homing capacit”
- Skewed maturation of memory HIV-specific CD8 T lymphocytes (2001, background): “We investigated this issue by analysing the expression of the chemokine receptor CCR7, which defines distinct subsets of naive and memory T lymphocytes with different homing and effector capacitie”