β1 integrins differentially control extravasation of inflammatory cell subsets into the CNS during autoimmunity

Inhibiting the α 4 subunit of the integrin heterodimers α 4 β 1 and α 4 β 7 with the monoclonal antibody natalizumab is an effective treatment for multiple sclerosis (MS). However, the pharmacological action of natalizumab is not understood conclusively. Previous studies suggested that natalizumab inhibits activation, proliferation, or extravasation of inflammatory cells. To specify which mechanisms, cell types, and α 4 heterodimers are affected by the antibody treatment, we studied MS-like experimental autoimmune encephalomyelitis (EAE) in mice lacking the β 1 -integrin gene either in all hematopoietic cells or selectively in T lymphocytes. Our results show that T cells critically rely on β 1 integrins to accumulate in the central nervous system (CNS) during EAE, whereas CNS infiltration of β 1 -deficient myeloid cells remains unaffected, suggesting that T cells are the main target of anti-α 4 -antibody blockade. We demonstrate that β 1 -integrin expression on encephalitogenic T cells is critical for EAE development, and we therefore exclude α 4 β 7 as a target integrin of the antibody treatment. T cells lacking β 1 integrin are unable to firmly adhere to CNS endothelium in vivo, whereas their priming and expansion remain unaffected. Collectively, these results suggest that the primary action of natalizumab is interference with T cell extravasation via inhibition of α 4 β 1 integrins.