4.4 Article

Vaccination with cetuximab mimotopes and biological properties of induced anti-epidermal growth factor receptor antibodies

Journal

JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
Volume 97, Issue 22, Pages 1663-1670

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/jnci/dji373

Keywords

-

Categories

Ask authors/readers for more resources

Background: The monoclonal antibody cetuximab (IMC-225, Erbitux) inhibits epidermal growth factor receptor (EGFR) signaling and has been approved for metastatic colon cancer therapy. However, to achieve effective titers, passive antibody therapies must be repeatedly administered over long periods. To overcome this limitation, we aimed to generate a vaccine inducing continuously available cetuximab-like antibodies in vivo using the mimotope approach. Methods: We used the phage display technique to identify four peptides structurally mimicking the cetuximab epitope. We coupled two of these peptides to an immunogenic carrier protein, and we vaccinated four groups (n = 8) of BALB/c mice intraperitoneally with 10 mu g of the mimotope conjugates, a control peptide conjugate, or the carrier protein alone. We assessed antibodydependent cellular cytotoxicity and complement-dependent cytotoxicity mediated by the induced antibodies against EGFR-overexpressing human A431 carcinoma cells. We then tested receptor internalization capacity of the induced antibodies with fluorescently labeled EGFR, and we assayed their growth inhibitory potential toward A431 cells with a [H-3]thymidine proliferation assay. Results: Mimotope-induced antibodies recognized EGFR, and both types of antibody-mediated cytotoxic effects were elicited by these antibodies. In both cellular cytotoxicity assays, the mimotope-induced antibodies exhibited specific lysis of more than 50%. The induced antibodies caused internalization of the receptor from the cell surface into endocytic vesicles and inhibited growth of EGFR-expressing cells to a similar extent as cetuximab [67% (95% confidence interval {CI} = 55% to 79%) and 69% (95% CI = 55% to 84%), respectively]. Conclusions: Epitope-specitic immunization is feasible for active anti-EGFR immunotherapy. The in vitro biologic features of mimotopeinduced antibodies are similar to those of the monoclonal antibody cetuximab.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available