| Literature DB >> 27832402 |
Sophia Franck1, Magdalena Paterka1, Jerome Birkenstock1, Frauke Zipp1, Volker Siffrin1, Esther Witsch2.
Abstract
Multiple sclerosis is a chronic, disseminated inflammation of the central nervous system which is thought to be driven by autoimmune T cells. Genetic association studies in multiple sclerosis and a large number of studies in the animal model of the disease support a role for effector/memory T helper cells. However, the mechanisms underlying relapses, remission and chronic progression in multiple sclerosis or the animal model experimental autoimmune encephalomyelitis, are not clear. In particular, there is only scarce information on the role of central nervous system-invading naive T helper cells in these processes. By applying two-photon laser scanning microscopy we could show in vivo that antigen unexperienced T helper cells migrated into the deep parenchyma of the inflamed central nervous system in experimental autoimmune encephalomyelitis, independent of their antigen specificity. Using flow cytometric analyses of central nervous system-derived lymphocytes we found that only antigen-specific, formerly naive T helper cells became activated during inflammation of the central nervous system encountering their corresponding antigen.Entities:
Keywords: Experimental autoimmune encephalomyelitis; Intravital two-photon microscopy; Migration; Multiple sclerosis; Naive TH cell
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Year: 2016 PMID: 27832402 DOI: 10.1007/s11481-016-9718-1
Source DB: PubMed Journal: J Neuroimmune Pharmacol ISSN: 1557-1890 Impact factor: 4.147