Leukocyte Recruitment in the Cerebrospinal Fluid of Mice with Experimental Meningitis Is Inhibited by an Antibody to Junctional Adhesion Molecule (Jam)

Author:

Del Maschio Aldo1,De Luigi Ada1,Martin-Padura Ines1,Brockhaus Manfred2,Bartfai Tamas2,Fruscella Paolo1,Adorini Luciano3,Martino GianVito4,Furlan Roberto4,De Simoni Maria Grazia1,Dejana Elisabetta15

Affiliation:

1. Istituto di Ricerche Farmacologiche “Mario Negri, ” 20157 Milan, Italy

2. F. Hoffmann-La Roche AG, CH-4070 Basel, Switzerland

3. Roche Milano Ricerche, 20132 Milan, Italy

4. DIBIT, 20132 Milan, Italy

5. Universita' degli Studi dell'Insubria, Dipartimento di Scienze Cliniche e Biologiche, Facolta' di Medicina e Chirurgia, 21100 Varese, Italy

Abstract

The mechanisms that govern leukocyte transmigration through the endothelium are not yet fully defined. Junctional adhesion molecule (JAM) is a newly cloned member of the immunoglobulin superfamily which is selectively concentrated at tight junctions of endothelial and epithelial cells. A blocking monoclonal antibody (BV11 mAb) directed to JAM was able to inhibit monocyte transmigration through endothelial cells in in vitro and in vivo chemotaxis assays. In this study, we report that BV11 administration was able to attenuate cytokine-induced meningitis in mice. The intravenous injection of BV11 mAb significantly inhibited leukocyte accumulation in the cerebrospinal fluid and infiltration in the brain parenchyma. Blood–brain barrier permeability was also reduced by the mAb. We conclude that JAM may be a new target in limiting the inflammatory response that accompanies meningitis.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

Reference34 articles.

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