Abstract | INTRODUCTION: AIM: DEVELOPMENT:
Fingolimod acts as an inverse agonist on sphingosine-1-phosphate receptors, inducing degradation of receptors. On lymphoid circulation, this effect causes retention in lymph nodes of naive and central memory T cells, including Th17 T lymphocytes, bearing CCR7 and CD62L receptors. As a result, the level of circulating T cells is markedly decreased. B ell circulation is impaired and complex effects on other immune cells are also induced. Fingolimod enters the central nervous system and binds to receptors on glial cells and neurons. In experimental autoimmune encephalomyelitis, the therapeutic efficacy of fingolimod is not only associated with a reduced entry of inflammatory cells into the nervous system, but also with a direct effect mostly on astroglial cells. CONCLUSIONS: In multiple sclerosis patients, the available evidence indicates that fingolimod efficacy is directly associated with impairment of circulation of several T cell subsets and possibly B cells. Animal studies raise the possibility that an additional effect on glial cells might also contribute to the clinical efficacy.
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Authors | J Antonio García-Merino, Antonio J Sánchez |
Journal | Revista de neurologia
(Rev Neurol)
Vol. 55
Issue 1
Pg. 31-7
(Jul 01 2012)
ISSN: 1576-6578 [Electronic] Spain |
Vernacular Title | Mecanismos basicos de accion del fingolimod en relacion con la esclerosis multiple. |
PMID | 22718407
(Publication Type: English Abstract, Journal Article)
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Chemical References |
- CCR7 protein, human
- Immunosuppressive Agents
- Lysophospholipids
- Propylene Glycols
- Receptors, CCR7
- Receptors, Lysosphingolipid
- L-Selectin
- sphingosine 1-phosphate
- Fingolimod Hydrochloride
- Sphingosine
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Topics |
- Animals
- Atrophy
- B-Lymphocytes
(drug effects, immunology)
- Brain
(immunology, pathology)
- Cell Movement
- Drug Evaluation, Preclinical
- Encephalomyelitis, Autoimmune, Experimental
(drug therapy)
- Fingolimod Hydrochloride
- Humans
- Immunosuppressive Agents
(chemistry, pharmacology, therapeutic use)
- L-Selectin
(analysis)
- Lysophospholipids
(physiology)
- Mice
- Molecular Structure
- Multiple Sclerosis
(drug therapy, immunology)
- Neuroglia
(drug effects, immunology)
- Propylene Glycols
(chemistry, pharmacology, therapeutic use)
- Rats
- Receptors, CCR7
(analysis)
- Receptors, Lysosphingolipid
(agonists)
- Sphingosine
(analogs & derivatives, chemistry, pharmacology, physiology, therapeutic use)
- T-Lymphocyte Subsets
(immunology)
- Th17 Cells
(drug effects, immunology)
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