T Lymphocyte/Eosinophil Interactions in Atopic Asthma: Critical Role for Interleukin-5 View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

1993

AUTHORS

A. B. Kay , Q. Hamid , D. D. Robinson , A. M. Bentley , A. Tsicopoulos , Sun Ying , R. Moqbel , C. J. Corrigan , S. R. Durham

ABSTRACT

Asthma is characterized by infiltration of the bronchial mucosa with large numbers of activated eosinophils and the presence of elevated concentrations of eosinophil-derived proteins such as major basic protein (Wardlaw et al. 1988) and the eosinophil cationic protein (De Monchy et al. 1985). The degree of the eosinophilia has been shown to correlate with the severity of airways hyperresponsiveness (Wardlaw et al. 1988, Durham et al. 1985). In a primate model of asthma, inhibition of the eosinophilic response to allergen substantially blocked the development of airways hyperresponsiveness (Wegner et al. 1990). Eosinophil-derived mediators have potential for producing many of the pathological features of asthma. For example, epithelial shedding might possibly occur through the cytotoxic effects of secreted eosinophil granule proteins (Gleich et al. 1979) and mucus hypersecretion and bronchoconstriction possibly through the release of platelet-activating factor (PAF) and leukotriene C4 (Holgate et al. 1989). Recent studies have also suggested a role for T lymphocytes in asthma. T lymphocyte infiltration is a feature of the late-phase response to allergen in atopic individuals in both the skin (Frew and Kay 1988) and lung (Metzger et al. 1987). More... »

PAGES

403-410

References to SciGraph publications

Book

TITLE

Progress in Immunology Vol. VIII

ISBN

978-3-642-51481-4
978-3-642-51479-1

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-642-51479-1_53

DOI

http://dx.doi.org/10.1007/978-3-642-51479-1_53

DIMENSIONS

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39 schema:description Asthma is characterized by infiltration of the bronchial mucosa with large numbers of activated eosinophils and the presence of elevated concentrations of eosinophil-derived proteins such as major basic protein (Wardlaw et al. 1988) and the eosinophil cationic protein (De Monchy et al. 1985). The degree of the eosinophilia has been shown to correlate with the severity of airways hyperresponsiveness (Wardlaw et al. 1988, Durham et al. 1985). In a primate model of asthma, inhibition of the eosinophilic response to allergen substantially blocked the development of airways hyperresponsiveness (Wegner et al. 1990). Eosinophil-derived mediators have potential for producing many of the pathological features of asthma. For example, epithelial shedding might possibly occur through the cytotoxic effects of secreted eosinophil granule proteins (Gleich et al. 1979) and mucus hypersecretion and bronchoconstriction possibly through the release of platelet-activating factor (PAF) and leukotriene C4 (Holgate et al. 1989). Recent studies have also suggested a role for T lymphocytes in asthma. T lymphocyte infiltration is a feature of the late-phase response to allergen in atopic individuals in both the skin (Frew and Kay 1988) and lung (Metzger et al. 1987).
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