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Pros and cons of different therapeutic antibody formats for recombinant antivenom development

Authors :
Felipe Augusto Cerni
Kristoffer H. Johansen
José María Gutiérrez
Bruno Lomonte
Andrea Martos-Esteban
Jonas A. Jürgensen
Erick Bermúdez-Méndez
Manuela Berto Pucca
Andreas Hougaard Laustsen
Line Ledsgaard
Mia Øhlenschlæger
Mikael Engmark
Cecilie Knudsen
Urska Pus
Mikael Rørdam Andersen
Johansen, Kristoffer [0000-0002-7711-9451]
Apollo - University of Cambridge Repository
Source :
Toxicon, vol.146, pp. 151-175., Kérwá, Universidad de Costa Rica, instacron:UCR, Laustsen, A H, Gutiérrez, J M, Knudsen, C, Johansen, K H, Bermúdez-Méndez, E, Cerni, F A, Jürgensen, J A, Jensen, L L, Martos Esteban, A, Øhlenschlæger, M, Pus, U, Andersen, M R, Lomonte, B, Engmark, M & Pucca, M B 2018, ' Pros and cons of different therapeutic antibody formats for recombinant antivenom development ', Toxicon, vol. 146, pp. 151-175 . https://doi.org/10.1016/j.toxicon.2018.03.004
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

Antibody technologies are being increasingly applied in the field of toxinology. Fuelled by the many advances in immunology, synthetic biology, and antibody research, different approaches and antibody formats are being investigated for the ability to neutralize animal toxins. These different molecular formats each have their own therapeutic characteristics. In this review, we provide an overview of the advances made in the development of toxin-targeting antibodies, and discuss the benefits and drawbacks of different antibody formats in relation to their ability to neutralize toxins, pharmacokinetic features, propensity to cause adverse reactions, formulation, and expression for research and development (R&D) purposes and large-scale manufacturing. A research trend seems to be emerging towards the use of human antibody formats as well as camelid heavy-domain antibody fragments due to their compatibility with the human immune system, beneficial therapeutic properties, and the ability to manufacture these molecules cost-effectively. Novo Nordisk Foundation/[16OC0019248]/NNF/Dinamarca Novo Nordisk Foundation/[13OC0005613]/NNF/Dinamarca Ministerio de Ciencia, Tecnología y Telecomunicaciones/[PEM-066-2015-II]/MICITT/Costa Rica Conselho Nacional de Desenvolvimento Científico e Tecnologico/[150749/2017-1]/CNPq/Brasil Universidad de Costa Rica/[OAICE-CAB-05-56-2016]/UCR/Costa Rica UCR::Vicerrectoría de Investigación::Unidades de Investigación::Ciencias de la Salud::Instituto Clodomiro Picado (ICP) UCR::Vicerrectoría de Docencia::Salud::Facultad de Microbiología

Details

Database :
OpenAIRE
Journal :
Toxicon, vol.146, pp. 151-175., Kérwá, Universidad de Costa Rica, instacron:UCR, Laustsen, A H, Gutiérrez, J M, Knudsen, C, Johansen, K H, Bermúdez-Méndez, E, Cerni, F A, Jürgensen, J A, Jensen, L L, Martos Esteban, A, Øhlenschlæger, M, Pus, U, Andersen, M R, Lomonte, B, Engmark, M & Pucca, M B 2018, ' Pros and cons of different therapeutic antibody formats for recombinant antivenom development ', Toxicon, vol. 146, pp. 151-175 . https://doi.org/10.1016/j.toxicon.2018.03.004
Accession number :
edsair.doi.dedup.....167bd03dabe7b720bac4fbf7b9a71d16
Full Text :
https://doi.org/10.17863/cam.24519