Selection of Candidate Monoclonal Antibodies for Therapy of Botulinum Toxin Type A Intoxications.
Natalia A ZeninskayaAlena K RyabkoMaksim A MarinTatyana I KombarovaMaria A ShkuratovaMethun M RogozinMarina V SilkinaYana O RomanenkoTatiana A IvashchenkoIgor G ShemyakinVictoria Valerievna FirstovaPublished in: Toxins (2024)
Botulism is one of the most serious food intoxications, manifesting as prolonged paralytic conditions. This disease is usually the result of the consumption of poor quality canned or smoked foods, so the inhabitants of many countries of the world are exposed to the risk of this kind of poisoning every year. In view of the severity of poisonings caused by botulinum neurotoxins, monoclonal antibodies (mAbs) show great promise because of their targeting action, lack of allergic reactions and serum sickness. The use of a cocktail of mAbs increases the "functional specificity" of their mixture, allowing them to bind to the active domains of different toxin chains and block their action. In this work, we obtained 14 murine mAbs to the catalytic and receptor-binding domain of botulinum toxin type A. The Sp2/0-Ag14 murine myeloma cell line and splenocytes from immunized mice of the BALB/c line were used as fusion partners. We have shown that the selected cocktail of three antibodies neutralizes native toxin more effectively than antibodies separately-complete neutralization is achieved at a toxin dose of 3LD50 and partial neutralization at 5LD50. We presume that this cocktail may be promising as a prototype for the creation of a therapeutic drug capable of neutralizing the toxin in the blood of patients.
Keyphrases
- botulinum toxin
- escherichia coli
- newly diagnosed
- end stage renal disease
- chronic kidney disease
- ejection fraction
- stem cells
- emergency department
- machine learning
- big data
- drug delivery
- patient reported outcomes
- highly efficient
- quality improvement
- high fat diet induced
- multiple myeloma
- binding protein
- bone marrow
- human immunodeficiency virus
- zika virus
- cell therapy
- adipose tissue
- adverse drug
- metabolic syndrome
- human health
- wild type
- dna binding
- artificial intelligence
- visible light
- replacement therapy