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Immunotherapeutic Effects of Recombinant Colorectal Cancer Antigen Produced in Tomato Fruits

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Journal Sci Rep
Specialty Science
Date 2022 Jun 13
PMID 35697846
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Abstract

The production of pharmacological vaccines in plants has been an important goal in the field of plant biotechnology. GA733-2, the protein that is also known as colorectal carcinoma (CRC)-associated antigen, is a strong candidate to produce a colorectal cancer vaccine. Tomato is the one of the major targets for production of an edible vaccine, as tomato is a fruit consumed in fresh form. It also contains high content of vitamins that aid activation of immune response. In order to develop an edible colorectal cancer vaccine, the transgene rGA733-Fc that encodes a fusion protein of GA733-2, the fragment crystallizable (Fc) domain, and the ER retention motif (rGA733-Fc) was introduced into tomato plants (Solanum lycopersicum cv. Micro-Tom). The transgenic plants producing rGA733-Fc (rGA733-Fc) protein were screened based on stable integration of transgene expression cassette and expression level of rGA733-Fc protein. Further glycosylation pattern analysis revealed that plant derived rGA733-Fc protein contains an oligomannose glycan structure, which is a typical glycosylation pattern found on ER-processing proteins. The red fruits of rGA733-Fc transgenic tomato plants containing approximately 270 ng/g FW of rGA733-Fc protein were orally administered to C57BL/6 mice. Oral administration of tomato fruits of the rGA733-Fc expressing transgenic plants delayed colorectal cancer growth and stimulated immune responses compared to oral administration of tomato fruits of the h-Fc expressing transgenic plants in the C57BL/6J mice. This is the first study showing the possibility of producing an edible colorectal cancer vaccine using tomato plants. This research would be helpful for development of plant-derived cancer edible vaccines.

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References
1.
Saxena M, van der Burg S, Melief C, Bhardwaj N . Therapeutic cancer vaccines. Nat Rev Cancer. 2021; 21(6):360-378. DOI: 10.1038/s41568-021-00346-0. View

2.
Ross A, Herlyn D, Iliopoulos D, KOPROWSKI H . Isolation and characterization of a carcinoma-associated antigen. Biochem Biophys Res Commun. 1986; 135(1):297-303. DOI: 10.1016/0006-291x(86)90976-9. View

3.
Fox J . Turning plants into protein factories. Nat Biotechnol. 2006; 24(10):1191-3. DOI: 10.1038/nbt1006-1191. View

4.
Spurr N, Durbin H, Sheer D, Parkar M, Bobrow L, Bodmer W . Characterization and chromosomal assignment of a human cell surface antigen defined by the monoclonal antibody AUAI. Int J Cancer. 1986; 38(5):631-6. DOI: 10.1002/ijc.2910380503. View

5.
Van Ree R, Akkerdaas J, Milazzo J, Loutelier-Bourhis C, Rayon C, Villalba M . Beta(1,2)-xylose and alpha(1,3)-fucose residues have a strong contribution in IgE binding to plant glycoallergens. J Biol Chem. 2001; 275(15):11451-8. DOI: 10.1074/jbc.275.15.11451. View