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Circulating levels of both Th1 and Th2 chemokines are elevated in patients with sarcoidosis

Authors :
Katsunori Sugisaki
Takuya Ueno
Tomiyasu Tsuda
Toshihide Kumamoto
Eishi Miyazaki
Tetsujiro Fukami
Masaru Ando
Shin-ichi Nureki
Source :
Respiratory Medicine. (2):239-247
Publisher :
Elsevier Ltd.

Abstract

Summary Background In sarcoidosis, the T helper type 1 (Th1) response tends to predominate at affected disease sites; however, whether Th1/Th2 polarization occurs in the peripheral circulation is unknown. Methods Fifty-two patients with sarcoidosis and 21 healthy volunteers were investigated. The concentrations of interferon-inducible protein 10 (IP-10)/CXCL10 and thymus- and activation-regulated chemokine (TARC)/CCL17 in the serum, bronchoalveolar lavage fluid (BALF) and culture supernatant were measured by an enzyme-linked immunosorbent assay. The circulating CXCR3+ CD4+ T cells and CCR4+ CD4+ T cells were assessed by flow cytometry. Results The CXCR3- or CCR4-positive ratios among CD4+ T cells were both higher in sarcoidosis than in healthy volunteers. The serum levels of both IP-10 and TARC of the patients with sarcoidosis were significantly higher than those of the healthy volunteers. In patients with sarcoidosis, a larger amount of IP-10 was generated by the BALF cells, whereas IP-10 production by peripheral blood mononuclear cells did not increase in comparison to the control subjects. The TARC levels produced by peripheral blood mononuclear cells of sarcoidosis patients were significantly higher than those of the controls, while no difference existed between the 2 groups regarding TARC production by BALF cells. Conclusion IP-10 is mainly produced at the lung and TARC in the peripheral circulation in sarcoidosis patients. Both IP-10 and TARC cooperatively play a role in the pathogenesis of sarcoidosis.

Details

Language :
English
ISSN :
09546111
Issue :
2
Database :
OpenAIRE
Journal :
Respiratory Medicine
Accession number :
edsair.doi.dedup.....02aaf0db5a4b9043b1997a07d1b8af58
Full Text :
https://doi.org/10.1016/j.rmed.2007.09.006