Stereoselective Synthesis of Sialyl Lewisa Antigen and the Effective Anticancer Activity of Its Bacteriophage Qβ Conjugate as an Anticancer Vaccine

Author:

Rashidijahanabad Zahra12,Ramadan Sherif123,O'Brien Nicholas A.4,Nakisa Athar12,Lang Shuyao12,Crawford Howard5,Gildersleeve Jeffrey C.4,Huang Xuefei126ORCID

Affiliation:

1. Department of Chemistry Michigan State University 48824 East Lansing Michigan USA

2. Institute for Quantitative Health Science and Engineering Michigan State University 48824 East Lansing Michigan USA

3. Chemistry Department Faculty of Science Benha University 13518 Benha Qaliobiya Egypt

4. Chemical Biology Laboratory Center for Cancer Research National Cancer Institute National Institutes of Health Frederick Maryland 21702 USA

5. Department of Surgery Henry Ford Health System Detroit Michigan 48202 USA

6. Department of Biomedical Engineering Michigan State University 48824 East Lansing Michigan USA

Abstract

AbstractSialyl Lewisa (sLea), also known as cancer antigen 19‐9 (CA19‐9), is a tumor‐associated carbohydrate antigen. The overexpression of sLea on the surface of a variety of cancer cells makes it an attractive target for anticancer immunotherapy. However, sLea‐based anticancer vaccines have been under‐explored. To develop a new vaccine, efficient stereoselective synthesis of sLea with an amine‐bearing linker was achieved, which was subsequently conjugated with a powerful carrier bacteriophage, Qβ. Mouse immunization with the Qβ‐sLea conjugate generated strong and long‐lasting anti‐sLea IgG antibody responses, which were superior to those induced by the corresponding conjugate of sLea with the benchmark carrier keyhole limpet hemocyanin. Antibodies elicited by Qβ‐sLea were highly selective toward the sLea structure, could bind strongly with sLea‐expressing cancer cells and human pancreatic cancer tissues, and kill tumor cells through complement‐mediated cytotoxicity. Furthermore, vaccination with Qβ‐sLea significantly reduced tumor development in a metastatic cancer model in mice, demonstrating tumor protection for the first time by a sLea‐based vaccine, thus highlighting the significant potential of sLea as a promising cancer antigen.

Funder

National Cancer Institute

Henry Ford Health System

Publisher

Wiley

Subject

General Medicine

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