| Literature DB >> 20739072 |
Alban Millonig1, Harald Hegen, Franziska Di Pauli, Rainer Ehling, Claudia Gneiss, Martina Hoelzl, Bettina Künz, Andreas Lutterotti, Dagmar Rudzki, Thomas Berger, Markus Reindl, Florian Deisenhammer.
Abstract
Vascular cell adhesion molecule-1 a ligand for leukocyte very late activating antigen-4 is a key player in leukocyte extravasation in MS lesions. Natalizumab a monoclonal antibody against VLA-4 blocks this interaction. VCAM-1 and its soluble form are up-regulated during endothelial activation in MS. We investigated the effect of Natalizumab on sVCAM-1 and VLA-4 on circulating leukocytes in MS patients. Natalizumab reduced levels of sVCAM-1 compared to controls (256 vs. 597 ng/mL). This effect was sustained and only reversed in patients with neutralizing antibodies against Natalizumab. Correspondingly Natalizumab diminished VLA-4 on leukocyte subsets. Our findings indicate that Natalizumab reduces transmigration not only by blocking VLA-4 but also by down-regulating VCAM-1.Entities:
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Year: 2010 PMID: 20739072 DOI: 10.1016/j.jneuroim.2010.07.012
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478