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Unique Subpopulations of CD56+ NK and NK-T Peripheral Blood Lymphocytes Identified by Chemokine Receptor Expression Repertoire

509

Citations

23

References

2001

Year

TLDR

CD56 is an immunophenotypic marker for several unique populations of peripheral blood lymphocytes, and CD56+ cells derived from multiple lymphocyte lineages share roles in immunosurveillance and antitumor responses. The study aims to characterize chemokine receptor expression patterns and migratory responses of three distinct CD56+ populations from human peripheral blood. The authors examined chemokine receptor expression and performed functional migration assays on these populations. NK‑T cells differ markedly from NK cells, CD16+ NK cells differ from CD16− NK cells; CD16+ NK cells predominantly respond to IL‑8 and fractalkine, NK‑T cells predominantly respond to the CCR5 ligand macrophage‑inflammatory protein‑1β, and CD16− NK cells uniquely express trafficking molecules for homing into secondary lymphoid organs, indicating diverse trafficking patterns among CD56+ cells.

Abstract

Abstract CD56, an adhesion molecule closely related to neual cell adhesion molecule, is an immunophenotypic marker for several unique populations of PBLs. Although CD56+ cells derive from multiple lymphocyte lineages, they share a role in immunosurveillance and antitumor responses. We have studied the chemokine receptor expression patterns and functional migratory responses of three distinct CD56+ populations from human peripheral blood. NK-T cells were found to differ greatly from NK cells, and CD16+ NK cells from CD16− NK cells. CD16+ NK cells were the predominant population responding to IL-8 and fractalkine, whereas NK-T cells were the predominant population responding to the CCR5 ligand macrophage-inflammatory protein-1β. CD16− NK cells were the only CD56+ population that uniformly expressed trafficking molecules necessary for homing into secondary lymphoid organs through high endothelial venule. These findings describe a diverse population of cells that may have trafficking patterns entirely different from each other, and from other lymphocyte types.

References

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