Accumulation of CCR4‐expressing CD4+ T cells and high concentration of its ligands (TARC and MDC) in bronchoalveolar lavage fluid of patients with eosinophilic pneumonia
Background: Th2 cells are thought to be involved in eosinophilic inflammation of the lung. CC chemokine receptor 4 (CCR4) has been identified as a specific receptor for both thymus and activation‐regulated chemokine (TARC) and macrophage‐derived chemokine (MDC), and is preferentially expressed on Th...
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Published in | Allergy (Copenhagen) Vol. 58; no. 6; pp. 518 - 523 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Munksgaard International Publishers
01.06.2003
Blackwell |
Subjects | |
Online Access | Get full text |
ISSN | 0105-4538 1398-9995 |
DOI | 10.1034/j.1398-9995.2003.00149.x |
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Summary: | Background: Th2 cells are thought to be involved in eosinophilic inflammation of the lung. CC chemokine receptor 4 (CCR4) has been identified as a specific receptor for both thymus and activation‐regulated chemokine (TARC) and macrophage‐derived chemokine (MDC), and is preferentially expressed on Th2 cells.
Objective: Our aim was to evaluate the role of Th2 cells in the lung of patients with eosinophilic pneumonia (EP).
Methods: The concentrations of TARC, MDC, and interleukin (IL)‐5 were measured in bronchoalveolar lavage fluid (BALF) by ELISA. Proportion of CCR4‐expressing CD4+ T cells (CCR4+ CD4+ T cells) was determined by flow cytometry.
Results: TARC and MDC concentrations in BALF were higher in patients with EP than in normal subjects. The proportion of CCR4‐expressing cells among CD4+ T cells was higher in BALF than in peripheral blood of patients with EP. There was a significant correlation between the number of CCR4+ CD4+ T cells and the levels of TARC, MDC, and IL‐5 in BALF of patients with EP.
Conclusions: Our data suggest that Th2 cells, which express CCR4 and its ligands (TARC and MDC), contribute to the pathogenesis of EP in the lung. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 0105-4538 1398-9995 |
DOI: | 10.1034/j.1398-9995.2003.00149.x |