Impact of MK886 on eosinophil counts and phenotypic features in toxocariasis

Author(s)

Anibal, F. F. ; Rogerio, A. P. ; Malheiro, A. ; Machado, E. R. ; Martins-Filho, O. A. ; Andrade, M. C. ; Soares, E. G. ; Medeiros, A. I. ; Faccioli, L. H. ^[9]

• Document type: Journal article
• Source: Scandinavian Journal of Immunology; v. 65, n. 4, p. 344-352, Apr. 2007.
• Field of knowledge: Biological Sciences - Immunology

Abstract

Experimental toxocariasis was used as a model of eosinophil migration. Mice inoculated with 200 Toxocara canis eggs were treated with the leukotriene inhibitor MK886 (1 mg/kg/day). Eosinophils were counted in peripheral blood (PB), peritoneal cavity (PC) and bronchoalveolar lavage fluid (BALF) samples on post-infection days 3, 6, 12, 18, 24 and 36. Eosinophil expression of Mac-1 and VLA-4 was analysed in PB and PC samples. We found that T. canis infection induced systemic eosinophilia from post-infection day 3, peaking on days 6, 12 and 24 in PB, PC and BALF samples respectively. Eosinophilia was more pronounced in PB and PC samples than in BALF samples, and MK886 downregulated eosinophilia to varying degrees in the different sample types. In PB and PC samples, T. canis infection caused early upregulation of Mac-1 with late changes in the VLA-4 profile, whereas MK886 had opposite effects. The distinct time-dependent eosinophilia peaks and differential involvement of leukotrienes in integrin expression demonstrate that, despite the systemic eosinophilia triggered by T. canis infection, inflammatory responses vary by compartment. (AU)

• FAPESP's process: 02/12856-2 - Modulation of innate and acquired immune responses by leukotrienes and prostaglandins
• Grantee: Lúcia Helena Faccioli
• Support Opportunities: Research Projects - Thematic Grants