Macrophage-derived chemokine production by activated human T cells in vitro and in vivo: preferential association with the production of type 2 cytokines

Citation
G. Galli et al., Macrophage-derived chemokine production by activated human T cells in vitro and in vivo: preferential association with the production of type 2 cytokines, EUR J IMMUN, 30(1), 2000, pp. 204-210
Citations number
23
Categorie Soggetti
Immunology
Journal title
EUROPEAN JOURNAL OF IMMUNOLOGY
ISSN journal
00142980 → ACNP
Volume
30
Issue
1
Year of publication
2000
Pages
204 - 210
Database
ISI
SICI code
0014-2980(200001)30:1<204:MCPBAH>2.0.ZU;2-0
Abstract
Macrophage-derived chemokine (MDC), a potent chemoattractant for chronicall y activated Th2 lymphocytes, is constitutively expressed by dendritic cells , B cells, macrophages, and thymic medullary epithelial cells, whereas mono cytes, NK cells, and T lymphocytes produce MDC only upon appropriate stimul ation. In this study, we show in vitro MDC production also by activated T c ells, which preferentially associate with the production of Th2 cytokines, IL-4, IL-5, and IL-6, and inversely correlate with the production of the Th 1 cytokine, IFN-gamma. Moreover, high levels of MDC were detected in the se ra of the great majority of subjects suffering from mycosis fungoides/Sezar y syndrome or atopic dermatitis, which are considered as disorders characte rized by the predominant expansion and activation of Th2 cells, respectivel y. By contrast, serum MDC levels in subjects with multiple sclerosis or Cro hn's disease, which are characterized by a Th1 predominance, did not differ significantly from those of healthy controls. Finally, MDC expression was detected in the skin biopsy specimens of subjects with atopic dermatitis, w here it was expressed by both dendritic cells and T lymphocytes. Taken toge ther, these findings suggest that MDC production by activated T cells may o ccur both in vitro and in vivo, particularly in association with Th2 cytoki nes, thus providing an important amplification circuit for Th2-mediated res ponses.