Am. J. Respir. Crit. Care Med., Vol 153, No. 4, 04 1996, 1398-1404.
Increased MCP-1, RANTES, and MIP-1alpha in bronchoalveolar lavage fluid of allergic asthmatic patients
R Alam, J York, M Boyars, S Stafford, JA Grant, J Lee, P Forsythe, T Sim and N Ida
Department of Internal Medicine, University of Texas Medical Branch, Galveston, USA.
Chemokines are cytokines that induce chemotaxis of inflammatory cells. We
studied the presence of chemokines in bronchoalveolar lavage fluid (BALF)
obtained from nine allergic asthmatic patients and six nonsmoking normal
individuals. The cells were pelleted, and ribonucleic acid (RNA) was
extracted by using RNAzol B. BALF was assayed for monocyte chemoattractant
protein-1 (MCP-1), regulated upon activation in normal T cells, expressed,
probably secreted (RANTES), macrophage inflammatory protein-1alpha
(MIP-1alpha) and interleukin-8 (IL-8) by enzyme-linked immunosorbent assay
(ELISA). The levels of MCP-1, RANTES, and MIP-1alpha were significantly
higher in the asthma patients than in the control subjects (p<0.04). The
concentrations of RANTES and MCP-1 correlated with the lymphocyte count in
the BAL specimens (r = 0.61 and 0.68, respectively). BALF showed eosinophil
chemotactic activity in vitro that was blocked by anti-RANTES and
anti-MCP-3 antibodies. The total cellular RNA was reverse-transcribed and
the complementary deoxyribonucleic acid (cDNA) was amplified with the
polymerase chain reaction (PCR) for MCP-1, MCP-3, RANTES, MIP-1alpha, IL-8,
and beta- actin. We found that messenger ribonucleic acids (mRNAs) for
MCP-1, MCP- 3, RANTES, MIP-1alpha, and IL-8 were produced by BAL cells from
most asthmatic and normal subjects. We conclude that chemokines are
produced in the airways, and that an increased recovery of MCP-1, RANTES,
and MIP-1alpha is observed in allergic asthmatic patients.
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[Abstract]
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T. Mirzadegan, F. Diehl, B. Ebi, S. Bhakta, I. Polsky, D. McCarley, M. Mulkins, G. S. Weatherhead, J.-M. Lapierre, J. Dankwardt, et al.
Identification of the Binding Site for a Novel Class of CCR2b Chemokine Receptor Antagonists. BINDING TO A COMMON CHEMOKINE RECEPTOR MOTIF WITHIN THE HELICAL BUNDLE
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[Abstract]
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I. Sabroe, M. J. Peck, B. J. Van Keulen, A. Jorritsma, G. Simmons, P. R. Clapham, T. J. Williams, and J. E. Pease
A Small Molecule Antagonist of Chemokine Receptors CCR1 and CCR3. POTENT INHIBITION OF EOSINOPHIL FUNCTION AND CCR3-MEDIATED HIV-1 ENTRY
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[Abstract]
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Copyright © 1996 American Thoracic Society
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