Kinetics of Eotaxin Generation and Its Relationship to Eosinophil Accumulation in Allergic Airways Disease: Analysis in a Guinea Pig Model In Vivo

Alison A. Humbles(Imperial College London), Dolores M. Conroy(Imperial College London), Sylvie Marleau(Imperial College London), Sara M. Rankin(Imperial College London), Roger Palframan(Imperial College London), Amanda E. I. Proudfoot(Imperial College London), Timothy N. C. Wells(Imperial College London), Dechun Li(Imperial College London), Peter K. Jeffery(Imperial College London), David A. Griffiths-Johnson(Imperial College London), Timothy J. Williams(Imperial College London), Peter J. Jose(Imperial College London)
The Journal of Experimental Medicine
August 18, 1997
Cited by 255Open Access
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Abstract

Challenge of the airways of sensitized guinea pigs with aerosolized ovalbumin resulted in an early phase of microvascular protein leakage and a delayed phase of eosinophil accumulation in the airway lumen, as measured using bronchoalveolar lavage (BAL). Immunoreactive eotaxin levels rose in airway tissue and BAL fluid to a peak at 6 h falling to low levels by 12 h. Eosinophil numbers in the tissue correlated with eotaxin levels until 6 h but eosinophils persisted until the last measurement time point at 24 h. In contrast, few eosinophils appeared in BAL over the first 12 h, major trafficking through the airway epithelium occurring at 12-24 h when eotaxin levels were low. Constitutive eotaxin was present in BAL fluid. Both constitutive and allergen-induced eosinophil chemoattractant activity in BAL fluid was neutralized by an antibody to eotaxin. Allergen-induced eotaxin appeared to be mainly in airway epithelium and macrophages, as detected by immunostaining. Allergen challenge of the lung resulted in a rapid release of bone marrow eosinophils into the blood. An antibody to IL-5 suppressed bone marrow eosinophil release and lung eosinophilia, without affecting lung eotaxin levels. Thus, IL-5 and eotaxin appear to cooperate in mediating a rapid transfer of eosinophils from the bone marrow to the lung in response to allergen challenge.


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