Abstract | BACKGROUND: There is increasing evidence supporting that neuromyelitis optica (NMO) is an inflammatory humoral mediated disorder associated with NMO- IgG/AQP-4 antibodies. However, little is known about the subsets of B cells and T cells that contribute to the pathogenesis or therapy response. OBJECTIVES: METHODS: We sequentially analysed the levels of NMO- IgG/AQP-4 by immunohistochemistry, and B and T cells subsets by multiparametric flow-cytometry, in the CSF and peripheral blood (PB), before and alter IV-Igs plus RTX therapy. RESULTS: In the CSF before treatment, and compared with PB, there was a higher percentage of CD4(+) T cells and a lower percentage of CD8(+) T cells and CD19(+) B cells. After therapy, the percentage of CD4(+) T cells remained high, and that of CD8(+) T cells increased. The observed decrease in the percentage of CD19(+) B cells was lower than in the PB. When the CSF was compared, it was found that the percentage of effector-memory and effector CD8(+) T cells had increased after therapy, and that of IgM memory B cells and switched-memory B cells decreased. The observed changes paralleled the decrease of NMO- IgG/AQP-4 results to negative and the clinical improvement. CONCLUSIONS: Our findings confirm that, besides intrathecal humoral immune response against AQP4, B and T cell subsets are involved in the modulation of inflammation within and outside the central nervous system.
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Authors | C de Andrés, R Teijeiro, A Saiz, P Fernández, S Sánchez-Ramón |
Journal | Neurologia (Barcelona, Spain)
(Neurologia)
Vol. 30
Issue 5
Pg. 276-82
(Jun 2015)
ISSN: 1578-1968 [Electronic] Spain |
PMID | 24674779
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright © 2013 Sociedad Española de Neurología. Published by Elsevier España, S.L.U. All rights reserved. |
Chemical References |
- AQP4 protein, human
- Aquaporin 4
- Autoantibodies
- Immunoglobulins, Intravenous
- Immunologic Factors
- Rituximab
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Topics |
- Adolescent
- Aquaporin 4
(immunology)
- Autoantibodies
(blood)
- B-Lymphocyte Subsets
(immunology)
- CD8-Positive T-Lymphocytes
(immunology)
- Drug Therapy, Combination
- Female
- Humans
- Immunoglobulins, Intravenous
(therapeutic use)
- Immunologic Factors
(therapeutic use)
- Neuromyelitis Optica
(cerebrospinal fluid, drug therapy, immunology)
- Rituximab
(therapeutic use)
- Spinal Cord
(immunology, pathology)
- T-Lymphocyte Subsets
(immunology)
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