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Feasibility study to determine whether new generation catalytic antibodies can overcome existing limitations for future use in clinical settings.

Feasibility study to determine whether new generation catalytic antibodies can overcome existing limitations for future use in clinical settings.
可行性研究,以确定新一代催化抗体是否可以克服现有的限制,以便将来在临床环境中使用。
批准号:
BB/N012356/1
负责人:
Nigel Scrutton
金额:
$15.22万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2016
资助国家:
英国
项目状态:
已结题
起止时间:
2016 至 --

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中文摘要
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英文摘要
Research into the therapeutic use of catalytic antibodies stretches back over 30 years but to date there is not a single example of success in the clinic. This is in stark contrast to the ever-expanding use of antibodies to treat a range of diseases when they are used as binders and modulators of protein function. This feasibility study aims to answer whether this imbalance can be redressed through the utilisation of novel techniques now available in antibody research (specifically improved antibody phage libraries and bispecific antibody technologies) combined with an examination of the therapeutic and commercial potential of catalytic antibodies should the primary issues of poor catalytic efficiency and selectivity as compared to the natural enzymes be addressed. As a test case we have chosen to try and make catalytic antibodies that share the therapeutically useful properties of streptococcal IgG endopeptidase but lack the enzyme's immunogenicity, which seriously limits its clinical potential.
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