specificity of mimotope-induced anti-high molecular weight-melanoma associated antigen (hmw-maa) antibodies does not ensure biological activity特异性mimotope-induced卤分子weight-melanoma相关抗原(hmw-maa)抗体不能确保生物活性.pdfVIP
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specificity of mimotope-induced anti-high molecular weight-melanoma associated antigen (hmw-maa) antibodies does not ensure biological activity特异性mimotope-induced卤分子weight-melanoma相关抗原(hmw-maa)抗体不能确保生物活性
Specificity of Mimotope-Induced Anti-High Molecular
Weight-Melanoma Associated Antigen (HMW-MAA)
Antibodies Does Not Ensure Biological Activity
1. 1. 1 1 1 2
Julia Latzka , Sonja Gaier , Gerlinde Hofstetter , Nina Balazs , Ursula Smole , Soldano Ferrone , Otto
1 1 3 1
Scheiner , Heimo Breiteneder , Hubert Pehamberger , Stefan Wagner *
1 Department of Pathophysiology and Allergy Research, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria,
2 Department of Surgery, of Immunology and of Pathology, University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania, United States of America, 3 Division of
General Dermatology, Department of Dermatology, Medical University of Vienna, Vienna, Austria
Abstract
Vaccines based on peptide mimics (mimotopes) of conformational tumor antigen epitopes have been investigated for a
variety of human tumors including breast cancer, tumors expressing the carcinoembryonic antigen, B cell lymphoma,
neuroblastoma, and melanoma. In our previous work, we designed a vaccine based on a mimotope of the high molecular
weight-melanoma associated antigen (HMW-MAA) that elicited HMW-MAA-specific antibodies (Abs) with anti-tumor activity
in vitro and in vivo. In this study, we aimed to identify mimotopes of additional distinct HMW-MAA epitopes, since they
could be used to construct a polymimotope melanoma vaccine. For this purpose, random peptide phage libraries were
screened with the anti-HMW-MAA monoclonal antibodies (mAbs) VT80.12 and VF1-TP43 yielding one peptide ligand for
each mAb. Both peptides inhibited the binding of the correspondin
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