[Design of equine serum-based Marburg virus immunoglobulin].
Abstract: Immunoglobulin (Ig) against Marburg fever (MF) has been obtained from the equine serum. In terms of physicochemical and immunobiological properties, the obtained preparation corresponds to the quality of heterologous commercial immunoglobulins. The application of Marburg virus (MV) Ig with a titer of no less than 1:2048 by the emergency prevention scheme 1-2 hours after intraperitoneal inoculation of guinea pigs with MV in a dose of 20-50 LD50 protected 88-100% of the animals from death. MV Ig is recommended for emergency prevention of human MF.
Publication Date: 2008-03-06 PubMed ID: 18318136
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- English Abstract
- Journal Article
Summary
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The research article focuses on the creation of immunoglobulin, derived from horse serum, to counteract Marburg Fever. The produced immunoglobulin matched the quality of similarly made commercial products and when applied immediately after the infection of guinea pigs with the Marburg virus, the majority of the animals survived.
Immunoglobulin Generation
- The study’s main component is the creation of an immunoglobulin (Ig) constructed from horse serum to target Marburg Fever (MF).
- The produced immunoglobulin, an antibody molecule with a specific amino acid sequence and produced by the immune system in response to a unique antigen, was assessed against the physicochemical and immunobiological characteristics of commercially available heterologous immunoglobulins.
- The findings were that the generated antibody was of comparable quality, suggesting that equine-derived immunoglobulins may be utilized for human diseases.
Functionality Assessment
- Following the generation of the antigen-specific Ig, the next phase of the investigation explored its effectiveness at preventing infection.
- The procedure involved intraperitoneally injecting guinea pigs with Marburg virus (MV) in a quantity known to be lethal (20-50 times the lethal dose, 50% – LD50).
- The experimental immunoglobulin was then applied 1-2 hours post inoculation to evaluate its efficacy for emergency prophylaxis.
- The results were promising, with 88-100% of the animals surviving, suggesting that immediate post-infection treatment with the immunoglobulin provided protection.
Recommendation and Potential
- Due to the promising in-vivo results in their study, the research team suggests the use of MV Ig for human MF emergency prevention.
- A successful translation of this treatment to humans could offer a significant breakthrough for managing and preventing the Marburg virus in emergency situations.
- Further studies are likely needed to validate these findings in other animal models and eventually in humans, as well as to understand any potential side effects of the treatment.
Cite This Article
APA
Borisevich IV, Potryvaeva NV, Mel'nikov SA, Evseev AA, Krasnianskiĭ VP, Maksimov VA.
(2008).
[Design of equine serum-based Marburg virus immunoglobulin].
Vopr Virusol, 53(1), 39-41.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Antibodies, Viral / blood
- Antibodies, Viral / immunology
- Antibody Specificity
- Guinea Pigs
- Horses
- Immunization
- Immunoglobulins / administration & dosage
- Immunoglobulins / blood
- Immunoglobulins / immunology
- Injections, Intraperitoneal
- Marburg Virus Disease / blood
- Marburg Virus Disease / prevention & control
- Marburgvirus / immunology
- Mice
- Neutralization Tests
- Papio
- Rabbits
- Time Factors
Citations
This article has been cited 3 times.- Mehedi M, Groseth A, Feldmann H, Ebihara H. Clinical aspects of Marburg hemorrhagic fever. Future Virol 2011 Sep;6(9):1091-1106.
- Bradfute SB, Bavari S. Correlates of immunity to filovirus infection. Viruses 2011 Jul;3(7):982-1000.
- Ristanović ES, Kokoškov NS, Crozier I, Kuhn JH, Gligić AS. A Forgotten Episode of Marburg Virus Disease: Belgrade, Yugoslavia, 1967. Microbiol Mol Biol Rev 2020 May 20;84(2).
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