Abstract | BACKGROUND: METHODS:
IgG was purified from serum of five controls without treatment, as well as from serum of 16 CIDP patients, two patients with Miller Fisher syndrome (MFS), and one patient with myasthenia gravis before and after treatment with IVIg. IgG dimer levels were determined by size exclusion chromatography. IgG dimer formation was correlated with clinical response to IVIg treatment in CIDP. Re-monomerized IgG dimer fractions were analyzed for immunoreactivity against peripheral nerve tissue. RESULTS:
IgG dimer levels were significantly higher in post- compared to pre- IVIg infusion samples. Low post-treatment IgG dimer levels in CIDP patients were associated with clinical worsening during IVIg treatment. Re-monomerized IgG dimer fractions from CIDP patients showed immunoreactivity against peripheral nerve tissue, whereas similarly treated samples from MFS patients showed immunoreactivity against GQ1b. CONCLUSION: Assessment of IgG dimer levels could be a novel approach to monitor CIDP patients during IVIg treatment, but further studies in larger cohorts are warranted to explore their utility to serve as a potential therapeutic biomarker for IVIg treatment response in CIDP.
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Authors | Christian Ritter, Ilja Bobylev, Helmar C Lehmann |
Journal | Journal of neuroinflammation
(J Neuroinflammation)
Vol. 12
Pg. 148
(Aug 14 2015)
ISSN: 1742-2094 [Electronic] England |
PMID | 26268846
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers
- Gangliosides
- Immunoglobulin G
- Immunoglobulins, Intravenous
- GQ1b ganglioside
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Topics |
- Aged
- Biomarkers
- Dimerization
- Female
- Gangliosides
(immunology)
- Humans
- Immunoglobulin G
(blood)
- Immunoglobulins, Intravenous
(therapeutic use)
- Male
- Middle Aged
- Miller Fisher Syndrome
(drug therapy, immunology)
- Myasthenia Gravis
(drug therapy)
- Nerve Fibers
(immunology)
- Peripheral Nerves
(pathology)
- Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
(blood, immunology, pathology)
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