John Robert Adair
Boehringer Ingelheim
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Featured researches published by John Robert Adair.
Human antibodies | 1994
John Robert Adair; Diljeet Singh Athwal; Mark William Bodmer; Susan Margaret Bright; Alexander M. Collins; Virginia L. Pulito; Patricia E. Rao; Roweena Reedman; Annette L. Rothermel; Danlin Xu; Robert A. Zivin; Linda Jolliffe
OKT3 is a murine monoclonal antibody which recognizes an epitope on the epsilon-subunit within the human CD3 complex. OKT3 possesses potent immunosuppressive properties in vivo and has been proven effective in the treatment of renal, heart and liver allograft rejection. Despite its efficacy, significant problems remain associated with OKT3 therapy, i.e. T-cell activation and the anti-murine antibody response. To address the problem of the anti-murine antibody response we have constructed humanized versions of OKT3. One of the humanized derivatives, gOKT3-7 incorporating the OKT3 complementarity determining regions plus a small number of alterations to the human framework, has an affinity of 1.4 x 10(9) M-1 compared with 1.2 x 10(9) M-1 for the murine OKT3. A humanized antibody (gOKT3-1) incorporating only the CDRs from OKT3 was found to be functionally inactive, confirming the requirement for nonCDR substitutions. gOKT3-7 retains the ability of mOKT3 to induce T cell proliferation in vitro and appears to be a good candidate for further development for in vivo therapy.
Expert Opinion on Investigational Drugs | 1995
John Robert Adair; Susan Margaret Bright
(1995). Monthly Update: Biologicals & Immunologicals: Progress with humanised antibodies - An update. Expert Opinion on Investigational Drugs: Vol. 4, No. 9, pp. 863-870.
Immunology Today | 1991
Susan Margaret Bright; John Robert Adair; David Secher
Access to a wide range of high quality and increasingly sophisticated reagents and equipment has underpinned the great surge of knowledge in basic immunology and the growing interest in clinical immunointervention. In this article, the first in an occasional series on immunological research and development in industry, Sue Bright and colleagues outline the key steps in a development programme to take a humanized monoclonal antibody into the clinic. The procedures involved in developing such reagents, particularly for clinical use, are long and require considerable ingenuity and scientific creativity.
Expert Opinion on Investigational Drugs | 1999
Paul B Rodgers; William Do Hamilton; John Robert Adair
The production of recombinant proteins in plants is reviewed with a particular focus on plant-derived vaccines and antibodies for human healthcare. Issues relating to foreign gene expression, such as protein yield, localisation and glycosylation are also considered. Emphasis is placed on reporting progress with preclinical and clinical evaluation of plant-derived vaccines and antibodies. An assessment is made of the likely future direction of research and development in this area.
Archive | 1995
John Robert Adair; Mark William Bodmer; Andrew Mountain; Raymond J. Owens
Archive | 1991
John Robert Adair; Diljeet Singh Athwal; John Spencer Emtage; Mark William Bodmer
Archive | 1990
Linda Jolliffe; Robert A. Zivin; John Robert Adair; Diljeet Singh Athwal
Archive | 1988
Mark William Bodmer; John Robert Adair; Nigel Whittle; Alan Howard Lyons; Raymond J. Owens
Archive | 1991
John Robert Adair; Martyn Kim Robinson; Susan Margaret Bright; Robert Rothlein
Archive | 1992
John Robert Adair; Raymond J. Owens; Terence Seward Baker; Alan Howard Lyons; Philip Ross Hamann; Ana T. Menendez; Lois Hinman