© The Rockefeller University Press, 0022-1007/1999/11/1351/ $5.00
The Journal of Experimental Medicine, Volume 190, Number 9, November 1, 1999 1351-1356
Leukocyte Recruitment in the Cerebrospinal Fluid of Mice with Experimental Meningitis Is Inhibited by an Antibody to Junctional Adhesion Molecule (Jam)
Aldo Del Maschioa,
Ada De Luigia,
Ines Martin-Paduraa,
Manfred Brockhause,
Tamas Bartfaie,
Paolo Fruscellaa,
Luciano Adorinic,
GianVito Martinob,
Roberto Furlanb,
Maria Grazia De Simonia, and
Elisabetta Dejanaa,d
a Istituto di Ricerche Farmacologiche "Mario Negri, " 20157 Milan, Italy
b DIBIT, 20132 Milan, Italy
c Roche Milano Ricerche, 20132 Milan, Italy
d Universita' degli Studi dell'Insubria, Dipartimento di Scienze Cliniche e Biologiche, Facolta' di Medicina e Chirurgia, 21100 Varese, Italy
e F. Hoffmann-La Roche AG, CH-4070 Basel, Switzerland
Istituto di Ricerche Farmacologiche "Mario Negri," Via Eritrea 62, 20157 Milano, Italy.39-02-354627739-02-390141
dejana{at}irfmn.mnegri.it
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.
Key Words: endothelium tight junction meningitis vascular permeability blood–brain barrier
© 1999 The Rockefeller University Press

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