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Updated: Jul 15, 2026

Myelin Oligodendrocyte Glycoprotein (MOG35-55) Induced Experimental Autoimmune Encephalomyelitis (EAE) in C57BL/6 Mice
Published on: April 15, 2014
Hyperimmune goat serum for amyotrophic lateral sclerosis
R Mackenzie1, M Kiernan, D McKenzie
1Institute of Neurological Sciences, Prince of Wales Hospital, High St, Randwick NSW 2031, Australia. macra@optushome.com.au
This study observed that hyperimmune goat serum (HGS) may slow respiratory muscle decline in amyotrophic lateral sclerosis (ALS) patients. Treatment with HGS showed a reduced rate of deterioration compared to the period before treatment.
Area of Science:
- Neurology
- Immunology
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting motor neurons.
- Respiratory muscle weakness is a primary cause of morbidity and mortality in ALS patients.
Observation:
- A single patient with ALS was treated with hyperimmune goat serum (HGS).
- Respiratory function tests (RFTs) were monitored over time to assess respiratory muscle strength.
- Measurements were standardized as a percentage of normal predicted values.
Findings:
- Respiratory muscle strength decline slowed significantly during 13 months of HGS treatment (1.3% per month) compared to the preceding 13 months (2.3% per month).
- The observed rate of decline under HGS treatment was notably less than expected for ALS progression and literature comparisons (4-5% decline per month).
Implications:
- Hyperimmune goat serum (HGS) may represent a potential therapeutic agent for slowing respiratory decline in ALS.
- Further research is warranted to validate these findings in a larger cohort of ALS patients.
- This study highlights the importance of monitoring respiratory function in ALS management.
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