Abstract |
Although intravenous immunoglobulin ( IVIG) has been reported to improve the status of expanded disability status scale (EDSS) of multiple sclerosis (MS) patients and reduce the annual relapse rate, some studies did not find its beneficial effects. In the present study, using an animal model for MS, we found that prophylactic, but not therapeutic, treatment successfully suppressed the disease development. During the search for factors involved in the disease suppression by IVIG, we obtained evidence suggesting that IVIG exerts its function, at least in part, by suppressing activation of matrix metalloproteinases (MMP)-2 and -9. Gelatin zymography revealed that gelatinase activities were suppressed by IVIG treatment in the spinal cord, but not in plasma. This finding raises the possibility that IVIG blocks MMP activities at the interface between the blood stream and CNS. With in situ zymography, we also observed that gelatinase activities were expressed mainly in astrocytes in the inflamed spinal cord of control rats and that this expression was attenuated by the treatment. These findings provide useful information to set optimal conditions for IVIG treatment of MS and to obtain more beneficial effects.
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Authors | Naoko Niimi, Kuniko Kohyama, Shintaro Kamei, Yoh Matsumoto |
Journal | Neuropathology : official journal of the Japanese Society of Neuropathology
(Neuropathology)
Vol. 31
Issue 4
Pg. 392-400
(Aug 2011)
ISSN: 1440-1789 [Electronic] Australia |
PMID | 21175863
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2010 Japanese Society of Neuropathology. |
Chemical References |
- Immunoglobulins, Intravenous
- Matrix Metalloproteinases
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Topics |
- Animals
- Encephalomyelitis, Autoimmune, Experimental
(drug therapy, metabolism, prevention & control)
- Immunoglobulins, Intravenous
(therapeutic use)
- Inflammation
(drug therapy, metabolism, prevention & control)
- Matrix Metalloproteinases
(metabolism)
- Multiple Sclerosis
(drug therapy, metabolism, prevention & control)
- Rats
- Spinal Cord
(metabolism)
- Treatment Outcome
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