View source for Antibody-Directed Enzyme Prodrug Therapy

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==Overview==
ADEPT (Antibody-directed enzyme prodrug therapy)<ref name="a1"> Bagshawe KD. Antibody-directed enzyme prodrug therapy (ADEPT) for cancer. Expert Rev Anticancer Ther. 2006; 6(10): 1421-1431.{{Entrez Pubmed|17069527}}</ref> is a strategy to overcome the problems of lack of tumor selectivity. An antibody designed/developed against a tumor antigen is linked to an enzyme and injected to the blood, resulting in selective binding of the enzyme in the tumor. When the discrimination between tumor and normal tissue enzyme levels is sufficient, a prodrug is administrated into the blood circultion, which is converted to an active cytotoxic drug by the enzyme, only within the tumor. Selectivity is achieved by the tumor specificity of the antibody and by delaying prodrug administration until there is a large differential between tumor and normal tissue enzyme levels. 

ADEPT has shown antitumor activity in animal tumor models of human choriocarcinoma and colonic and breast carcinoma.

==ADEPT history==

The first pilot-scale clinical trial of ADEPT was carried out at Charing Cross Hospital, London, using an anti-CEA F(ab′)2 antibody conjugated to the bacterial enzyme carboxypeptidase G2 (CPG2)<ref name="m7"> KD Bagshawe, SK Sharma, CJ Springer and P Antoniw, Antibody directed enzyme prodrug therapy (ADEPT): a pilot scale clinical trial. Tumor Targeting 1 (1995) 17–29. </ref>.

The antibody used in the first ADEPT clinical trial was of murine origin and the enzyme was bacterial. Host antibodies to both components of the AEC were present in the blood of all non-immunosuppressed patients by day 10 after AEC infusion <ref name="m10"> KD Bagshawe and SK Sharma, Cyclosporin delays host immune response to antibody enzyme conjugate in ADEPT. Transplant Proc 28 (1996), 3156–3158. {{Entrez Pubmed|8962223}}</ref>. Several patients received cyclosporin since it had been shown in rabbits that this could delay the appearance of host antibodies to soluble proteins <ref name="m11"> JA Ledermann, RHJ Begent and KD Bagshawe, Cyclosporin A prevents the anti murine antibody response to a monoclonal antibody in rabbits. Br J Cancer 58 (1988), 562–566. </ref>.

A subsequent, small-scale trial at the Royal Free Hospital, London, used the same agents as in the Charing Cross Hospital trial but the protocol was modified to provide additional pharmacokinetic data and most patients received only a single course of treatment <ref name="m12"> KD Bagshawe and M Napier, Early clinical studies with ADEPT. In: RG Melton and RJ Knox Editors, Enzyme-Prodrug Strategies for Cancer Therapy Kluwer Academic, London (1999), 199–207. </ref>.

==Other versions of directed enzyme prodrug therapy (DEPT)== 
There are several other strategies to use prodrug/enzyme systems for cancer therapy, including gene-directed enzyme prodrug therapy (GDEPT), virus-directed enzyme prodrug therapy (VDEPT), PDEPT (Polymer-Directed Enzyme Prodrug Therapy), LEAPT (Lectin-directed enzyme-activated prodrug therapy)<ref name="m2">Silva AT, Chung MC, Castro LF, Guido RV, Ferreira EI. Advances in prodrug design. Mini Rev Med Chem. 5 (2005) 893-914.{{Entrez Pubmed|16250833}}</ref><ref name="m1"> Xu G, McLeod HL. Strategies for enzyme/prodrug cancer therapy. Clin Cancer Res. 7 (2001) 3314-24.{{Entrez Pubmed|11705842}}</ref>, and [[CDEPT]]<ref name="m5"> Minton NP. Clostridia in cancer therapy. Nat Rev Microbiol. 2003;1:237–42.{{Entrez Pubmed|15035028}}</ref> (Clostridial-directed enzyme prodrug therapy).

==References==
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[[Category:Cancer treatments]]
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