Elevated chemokine levels in bronchoalveolar lavage fluid of patients witheosinophilic pneumonia

Citation
S. Katoh et al., Elevated chemokine levels in bronchoalveolar lavage fluid of patients witheosinophilic pneumonia, J ALLERG CL, 106(4), 2000, pp. 730-736
Citations number
29
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
ISSN journal
00916749 → ACNP
Volume
106
Issue
4
Year of publication
2000
Pages
730 - 736
Database
ISI
SICI code
0091-6749(200010)106:4<730:ECLIBL>2.0.ZU;2-5
Abstract
Background: Allergic lung inflammation is caused by accumulation and activa tion of different leukocyte subsets, such as eosinophils and T lymphocytes, in the lung, The chemokines are a large group of chemotactic cytokines tha t regulate leukocyte trafficking and may play an important role in allergic lung inflammation. Objective: The purpose of this study was to evaluate the role of various ch emokines, including eotaxin, RANTES, monocyte chemotactic protein (MCP)-1, macrophage inflammatory protein (MIP)-1 beta, and IL-8 in the pathogenesis of eosinophilic pneumonia (EP). Methods: The concentrations of eotaxin, RANTES, MCP-1, MIP-1 beta, and IL-8 in bronchoalveolar lavage fluid (BALF) were measured by using ELISA in 15 patients with EP, 10 with idiopathic pulmonary fibrosis, 10 with sarcoidosi s, and 11 healthy volunteers. Results: Eotaxin in BALF was high only in patients with EP, and its level c orrelated significantly with the number of eosinophils in BALF of patients with EP and healthy volunteers. MCP-1 and MIP-1 beta in BALF were preferent ially increased in patients with EP. There was a significant correlation be tween MCP-1 levels and the number of macrophages in BALF of patients with E P and healthy volunteers. Conclusion: Our findings suggest that these CC chemokines contribute to the pathogenesis of EP through the specific recruitment of leukocyte subsets i n the lung.