Literature DB >> 10855785

Transgenic mice as a source of fully human antibodies for the treatment of cancer.

C G Davis1, M L Gallo, J R Corvalan.   

Abstract

The last two years have seen a renaissance of monoclonal antibodies for the treatment of disease. Of the eight antibodies currently approved for human therapy, two are for the treatment of cancer. In large part, the revival of antibodies has been driven by technology developments geared toward making antibodies less likely to elicit an anti-antibody response in humans. The development of transgenic mice, XenoMouse animals, capable of making fully human antibodies offers new opportunities for generating antibodies of therapeutic quality. Recently, this technology has been applied to the generation of a fully human antibody to the epidermal growth factor receptor. A description of the development of this antibody serves to illustrate the power and ease of use of XenoMouse technology.

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Year:  1999        PMID: 10855785     DOI: 10.1023/a:1006321231510

Source DB:  PubMed          Journal:  Cancer Metastasis Rev        ISSN: 0167-7659            Impact factor:   9.264


  5 in total

1.  Development of human-murine chimeric immunoglobulin G for use in the serological detection of human flavivirus and alphavirus antibodies.

Authors:  Brett A Thibodeaux; Amanda N Panella; John T Roehrig
Journal:  Clin Vaccine Immunol       Date:  2010-08-25

Review 2.  Strategies of targeting the extracellular domain of RON tyrosine kinase receptor for cancer therapy and drug delivery.

Authors:  Omid Zarei; Silvia Benvenuti; Fulya Ustun-Alkan; Maryam Hamzeh-Mivehroud; Siavoush Dastmalchi
Journal:  J Cancer Res Clin Oncol       Date:  2016-08-08       Impact factor: 4.553

3.  Development of a human-murine chimeric immunoglobulin M antibody for use in the serological detection of human flavivirus antibodies.

Authors:  Brett A Thibodeaux; John T Roehrig
Journal:  Clin Vaccine Immunol       Date:  2009-03-18

4.  SEAP expression in transiently transfected mammalian cells grown in serum-free suspension culture.

Authors:  Ernst-Jürgen Schlaeger; Eric A Kitas; Arnulf Dorn
Journal:  Cytotechnology       Date:  2003-05       Impact factor: 2.058

5.  Lymphocytes from enlarged iliac lymph nodes as fusion partners for the production of monoclonal antibodies after a single tail base immunization attempt.

Authors:  Yoshikazu Sado; Satoko Inoue; Yasuko Tomono; Hiroyuki Omori
Journal:  Acta Histochem Cytochem       Date:  2006-04-26       Impact factor: 1.938

  5 in total

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