The Ex Vivo Production of IL-6 and IL-21 by CD4+ T Cells is Directly Associated with Neurological Disability in Neuromyelitis Optica Patients

Neuromyelitis optica (NMO), also known as Devic’s disease, is an autoimmune, inflammatory disorder of the central nervous system (CNS) in which the immune system attacks myelin of the neurons located at the optic nerves and spinal cord, thus producing a simultaneous or sequential optic neuritis and...

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Published in:Journal of clinical immunology Vol. 33; no. 1; pp. 179 - 189
Main Authors: Linhares, Ulisses C., Schiavoni, Patrícia B., Barros, Priscila O., Kasahara, Taissa M., Teixeira, Bruna, Ferreira, Thais B., Alvarenga, Regina, Hygino, Joana, Vieira, Morgana M. M., Bittencourt, Vera Carolina B., Andrade, Regis M., Andrade, Arnaldo F., Bento, Cleonice A. M.
Format: Journal Article
Language:English
Published: Boston Springer US 2013
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Summary:Neuromyelitis optica (NMO), also known as Devic’s disease, is an autoimmune, inflammatory disorder of the central nervous system (CNS) in which the immune system attacks myelin of the neurons located at the optic nerves and spinal cord, thus producing a simultaneous or sequential optic neuritis and myelitis. The objective of this study was evaluated the background T-cell function of patients suffering from neuromyelitis optica (NMO), an autoimmune disorder of the central nervous system. In our study, the in vitro T cell proliferation and the production of Th1 cytokines were significantly lower in cell cultures from NMO patients, as compared with healthy individuals. In contrast, a dominant Th17-like phenotype, associate with higher IL-23 and IL-6 production by LPS-activated monocytes, was observed among NMO patients. The release of IL-21 and IL-6 by polyclonaly activated CD4 + T cells was directly correlated to neurological disability. In addition, the in vitro release of IL-21, IL-6 and IL-17 was significantly more resistant to glucocorticoid inhibition in NMO patients. In conclusion, the results indicate dominate Th17-related response in NMO patients that was directly proportional to neurological disability. Furthermore, our results can help to explain why NMO patients trend to be more refractory to corticoid treatment.
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ISSN:0271-9142
1573-2592
DOI:10.1007/s10875-012-9780-2