Engineering antibody fragments: replicating the immune system and beyond

Since genetic engineering of humanized murine monoclonal antibodies was fi rst demonstrated over two decades ago, antibody engineering technologies have evolved based upon an increasing understanding of the mechanisms involved in antibody generation in vivo, and a constant search for alternative rou...

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Autores:
García-Quiroz, F. (Felipe)
Sinclair, M. (Michael)
Tipo de recurso:
Article of journal
Fecha de publicación:
2010
Institución:
Universidad EIA .
Repositorio:
Repositorio EIA .
Idioma:
eng
OAI Identifier:
oai:repository.eia.edu.co:11190/484
Acceso en línea:
https://repository.eia.edu.co/handle/11190/484
Palabra clave:
RBI00073
TECNOLOGÍAS PARA LA SALUD
TECHNOLOGY IN HEALTH
ANTIBODIES - PHYSIOLOGY
ANTICUERPOS - FISIOLOGÍA
ANTIBODY ENGINEERING
PHASE DISPLAY
CELL DISPLAY
RIBOSOME DISPLAY
ANTIBODY HUMANIZATION
INGENIERIA DE ANTICUERPOS
PRESENTACION EN FAGOS
PRESENTACION EN CELULAS
PRESENTACION EN RIBOSOMAS
HUMANIZACION DE ANTICUERPOS
Rights
openAccess
License
Derechos Reservados - Universidad EIA, 2020
Description
Summary:Since genetic engineering of humanized murine monoclonal antibodies was fi rst demonstrated over two decades ago, antibody engineering technologies have evolved based upon an increasing understanding of the mechanisms involved in antibody generation in vivo, and a constant search for alternative routes to evolve and exploit the characteristics of antibodies. As a result, antibody engineers have devised innovative strategies for the rapid evolution and selection of antibodies and novel antibody designs (i.e., antibody fragments). Phage display, cell display and ribosome display technologies, which comprise the core of the currently available technologies for the discovery and preparation of such antibodies, are reviewed herein. This article intends to communicate the state-of-the-art technology available for the engineering of antibodies to a general readership interested in this important fi eld. Therefore, important immunology concepts are introduced before detailed descriptions of the three antibody engineering technologies are presented in later sections. A comparison of these methodologies suggests that despite the predominance of phage display for the engineering of antibody fragments in the past 20 years, cell display and ribosome display will likely gain importance in the selection and discovery of the antibody fragments in the future. Finally, these technologies are likely to play an important role in the production of the next generation of antibody-based therapeutics.