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Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases

The study of antibodies has been a focal point in modern biology and medicine since the early 1900s. However, progress in therapeutic antibody development was slow and intermittent until recently. The first antibody therapy, murine-derived murononab OKT3 for acute organ rejection, was approved by th...

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Detalles Bibliográficos
Autor principal: An, Zhiqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Higher Education Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875100/
https://www.ncbi.nlm.nih.gov/pubmed/21203944
http://dx.doi.org/10.1007/s13238-010-0052-8
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author An, Zhiqiang
author_facet An, Zhiqiang
author_sort An, Zhiqiang
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description The study of antibodies has been a focal point in modern biology and medicine since the early 1900s. However, progress in therapeutic antibody development was slow and intermittent until recently. The first antibody therapy, murine-derived murononab OKT3 for acute organ rejection, was approved by the US Food and Drug Administration (FDA) in 1986, more than a decade after César Milstein and Georges Köhler developed methods for the isolation of mouse monoclonal antibodies from hybridoma cells in 1975. As a result of the scientific, technological, and clinical breakthroughs in the 1980s and 1990s, the pace of therapeutic antibody discovery and development accelerated. Antibodies are becoming a major drug modality with more than two dozen therapeutic antibodies in the clinic and hundreds more in development. Despite the progress, need for improvement exists at every level. Antibody therapeutics provides fertile ground for protein scientists to fulfill the dream of personalized medicine through basic scientific discovery and technological innovation.
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spelling pubmed-48751002016-06-06 Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases An, Zhiqiang Protein Cell Review The study of antibodies has been a focal point in modern biology and medicine since the early 1900s. However, progress in therapeutic antibody development was slow and intermittent until recently. The first antibody therapy, murine-derived murononab OKT3 for acute organ rejection, was approved by the US Food and Drug Administration (FDA) in 1986, more than a decade after César Milstein and Georges Köhler developed methods for the isolation of mouse monoclonal antibodies from hybridoma cells in 1975. As a result of the scientific, technological, and clinical breakthroughs in the 1980s and 1990s, the pace of therapeutic antibody discovery and development accelerated. Antibodies are becoming a major drug modality with more than two dozen therapeutic antibodies in the clinic and hundreds more in development. Despite the progress, need for improvement exists at every level. Antibody therapeutics provides fertile ground for protein scientists to fulfill the dream of personalized medicine through basic scientific discovery and technological innovation. Higher Education Press 2010-04-01 2010-04 /pmc/articles/PMC4875100/ /pubmed/21203944 http://dx.doi.org/10.1007/s13238-010-0052-8 Text en © Higher Education Press and Springer-Verlag Berlin Heidelberg 2010
spellingShingle Review
An, Zhiqiang
Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title_full Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title_fullStr Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title_full_unstemmed Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title_short Monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
title_sort monoclonal antibodies — a proven and rapidly expanding therapeutic modality for human diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4875100/
https://www.ncbi.nlm.nih.gov/pubmed/21203944
http://dx.doi.org/10.1007/s13238-010-0052-8
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