The DOI matches its Crossref record; 129 of the 129 references it cites were found in a registry or an index.
Production platforms for biotherapeutic glycoproteins. Occurrence impact, and challenges of non-human sialylation
Open accessAbstract
One of the fastest growing fields in the pharmaceutical industry is the market for therapeutic glycoproteins. Today, these molecules play a major role in the treatment of various diseases, and include several protein classes, i.e., clotting factors, hormones, cytokines, antisera, enzymes, enzyme inhibitors, Ig-Fc-Fusion proteins, and monoclonal antibodies. Optimal glycosylation is critical for therapeutic glycoproteins, as glycans can influence their yield, immunogenicity and efficacy, which impact the costs and success of such treatments. While several mammalian cell expression systems currently used can produce therapeutic glycoproteins that are mostly decorated with human-like glycans, they can differ from human glycans by presenting two structures at the terminal and therefore most exposed position. First, natural human N-glycans are lacking the terminal Gal 1-3Gal (alpha-Gal) modification; and second, they do not contain the non-human sialic acid N-glycolylneuraminic acid (Neu5Gc). All humans spontaneously express antibodies against both of these glycan structures, risking increased immunogenicity of biotherapeutics carrying such non-human glycan epitopes. However, in striking contrast to the alpha-Gal epitope, exogenous Neu5Gc can be metabolically incorporated into human cells and presented on expressed glycoproteins in several possible epitopes. Recent work has demonstrated that this non-human sialic acid is found in widely varying amounts on biotherapeutic glycoproteins approved for treatment of various medical conditions. Neu5Gc on glycans of these medical agents likely originates from the production process involving the non-human mammalian cell lines and/or the addition of animal-derived tissue culture supplements. Further studies are needed to fully understand the impact of Neu5Gc in biotherapeutic agents. Similar concerns apply to human cells prepared for allo- or auto-transplantation, that have been grown in animal-derived tissue culture supplements.
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“Indeed, plants produce core α1,3-fructose and β1,2-xylose, which are completely absent in human cells and could be immunogenic (Karg et al., 2009;Ghaderi et al., 2012).”
From Therapeutic glycoprotein production in mammalian cells (2017) · cites this paper as Ghaderi et al., 2012
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Wiederschain, G. Y. (2009) · Biochemistry (Moscow) · doi:10.1134/s0006297909090156 · Cited by 4,089
Siglecs and their roles in the immune system
Crocker, P. R., Paulson, J. C., & Varki, A. P. (2007) · Nature reviews. Immunology · doi:10.1038/nri2056 · Cited by 2,032
Self-citationCetuximab-Induced Anaphylaxis and IgE Specific for Galactose-α-1,3-Galactose
Chung, C. H., Mirakhur, B., Chan, E., Le, Q.-T., Berlin, J., Morse, M., Murphy, B. A., Satinover, S. M., Hosen, J., Mauro, D., et al. (2008) · New England Journal of Medicine · doi:10.1056/nejmoa074943 · Cited by 1,521
The Impact of Glycosylation on the Biological Function and Structure of Human Immunoglobulins
Arnold, J. N., Wormald, M. R., Sim, R. B., Rudd, P. M., & Dwek, R. A. (2006) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141702 · Cited by 1,354
Chemical Diversity in the Sialic Acids and Related α-Keto Acids: An Evolutionary Perspective
Angata, T., & Varki, A. P. (2002) · Chemical Reviews · doi:10.1021/cr000407m · Cited by 1,254
Self-citationProduction of α1,3-Galactosyltransferase-Deficient Pigs
Phelps, C. J., Koike, C., Vaught, T. D., Boone, J. T., Wells, K. D., Chen, S.-H., Ball, S. F., Specht, S. M., Polejaeva, I. A., Monahan, J. A., et al. (2003) · Science · doi:10.1126/science.1078942 · Cited by 1,111
Baculovirus as versatile vectors for protein expression in insect and mammalian cells
Kost, T. A., Condreay, J. P., & Jarvis, D. L. (2005) · Nature Biotechnology · doi:10.1038/nbt1095 · Cited by 1,014
Human embryonic stem cells express an immunogenic nonhuman sialic acid
Martin, M. J., Muotri, A. R., Gage, F. H., & Varki, A. P. (2005) · Nature Medicine · doi:10.1038/nm1181 · Cited by 935
Self-citationJournal of the National Cancer Institute
(1993) · Journal of the American Dietetic Association · doi:10.1016/0002-8223(93)92324-q · Cited by 913
Wiseman, M. J. (2008) · Proceedings of The Nutrition Society · doi:10.1017/s002966510800712x · Cited by 902
Flagged first, then by citations
Research works printed but not linked: 7
- Borys MC, 2009, Biotechnol Bioeng
- Dahl SL, 2011, Sci Transl Med, 3
- Hanganutziu M, 1924, CR Séances Soc Biol, 91, 1457
- Higashi H, 1985, Cancer Research, 45, 3796
- Stanley P, 2009, Essentials of Glycobiology, 101
- Takiguchi M, 1984, Clin Exp Immunol, 56, 345
- Varki A, 2009, Essentials of Glycobiology, 281
Cited by
Sorted by citations
Items 301–321 of 321
Recombinant expression systems
(2015) · CRC Press eBooks · doi:10.1201/b19077-7
Systems glycoengineering of therapeutic proteins
Agatemor, C., Ha, L., Muthiah, K., Osman, A., Jukes, M., & Yarema, K. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-12-819655-7.00008-4
Plant Molecular Farming: Production of Virus-like Particles in Plants
Rutkowska, D. A. (2024) · Concepts and strategies in plant sciences · doi:10.1007/978-981-97-0176-6_2
Tobacco Plants as a Versatile Host for the Expression of Glycoproteins
Kittur, F. S., Wright, C., Hung, C., & Xie, J. (2024) · Concepts and strategies in plant sciences · doi:10.1007/978-981-97-0176-6_19
Biologic from mammalian and non-mammalian cell lines
Behera, B. K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15640-3.00005-7
Sharma, V., Guleria, R., & Mukherjee, K. J. (2026) · Indian Journal of Biochemistry and Biophysics · doi:10.56042/ijbb.v63i6.28419
An In Vivo Method for Biotinylation of Recombinant Variola Virus Proteins
Nikitin, V. N., Merkuleva, I. A., & Щербаков, Д. Н. (2024) · Applied Biochemistry and Microbiology · doi:10.1134/s0003683824605201
Peptides, Proteins and Antibodies
Gennaro, S. I. D., & Lalatsa, A. (2024) · Springer eBooks · doi:10.1007/978-3-031-59478-6_19
Yuan, X., Wu, Y., Zhang, Y., Yao, B., Zhang, L., Liu, Z., Ma, Q., & Ma, F. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110254
Mirfeizollahi, A., & Kaghazian, H. (2025) · Journal of Cellular Biotechnology · doi:10.1177/23523689251359487
Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques
Brachet, G. (2017) · theses.fr (ABES) · doi:10.70675/8a131ef8z9b1az469fzb97aze35914486b73
Influence des anticorps anti-Neu5Gc et anti-alpha-1-3-Galactose dans la réponse immunitaire
Rousse, J. (2019) · theses.fr (ABES) · doi:10.70675/4b032d03z011bz4593zba51zf37eb1e47a25
NS0 and CHO cell lines generate distinct quality profiles for non‐originator NISTmAbs
Bush, X., Azer, N., Kim, J., Powers, D. N., & Fratz‐Berilla, E. J. (2026) · Biotechnology Progress · doi:10.1002/btpr.88520
Structural and functional characterization of human kallistatin
Pham, S. T. D., Nielsen, K., Graversen, J. H., Kristensen, N., Steffensen, L. B., Lundgaard, A. R., Martı́n-Ventura, J. L., Højrup, P., & Palarasah, Y. (2026) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2026.102651
Chauhan, D., Shivach, T., & Rathore, A. (2026) · Journal of the American Society for Mass Spectrometry · doi:10.1021/jasms.6c00136
Grafinger, K. E., Gréen, H., Gallegos, A., de Morais, J., Planchuelo, G., & Stove, C. P. (2026) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2026.117945
Alrbyawi, H. (2026) · Pharmaceutics · doi:10.3390/pharmaceutics18091045
Glycosylation in Quality and Safety of Therapeutic Proteins
Matsumoto, Y., Kim, J., McKenna, K. R., Biel, T. G., Kirshner, S., Falkowski, V. M., & Ju, T. (2026) · Pharmacological Reviews · doi:10.1016/j.pharmr.2026.100163
Metadata
- Authors
- Ghaderi, D., Zhang, M., Hurtado-Ziola, N., & Varki, A.
- Affiliations
- University of California San Diego (US)
- Corresponding author
- Varki, Ajit
- Venue
- Biotechnology and Genetic Engineering Reviews
- Publisher
- Informa UK Limited
- Published
- 2012-01
- Volume
- 28
- Issue
- 1
- Pages
- 147-176
- ISSN
- 0264-8725 (ISSN-L)
- 2046-5556
- OpenAlex
- W1997984454
- Cited by
- 320
- References
- 128
- Citations by year
- 2026: 9 · 2025: 11 · 2024: 15 · 2023: 13 · 2022: 22 · 2021: 29 · 2020: 29 · 2019: 30 · 2018: 25 · 2017: 30 · 2016: 24 · 2015: 36 · 2014: 23 · 2013: 21 · 2012: 3
- FWCI
- 10.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Biotechnology and Genetic Engineering Reviews (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glycosylation and Glycoproteins Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Viral Infectious Diseases and Gene Expression in Insects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Transgenic Plants and Applications
- Keywords
- N-glycolylneuraminic acid, alpha-gal epitope, therapeutic glycoproteins, biologic therapy, N-glycosylation, immunogenicity, sialic acid, monoclonal antibodies
- MeSH terms
- Animals, Antibodies, Monoclonal, Epitopes, Biotechnology, Carbohydrate Sequence, Cattle, Cells, Cultured, Culture Media, Disaccharides, Glycoproteins, Glycosylation, Cricetinae, Humans, Insecta, Rabbits, Recombinant Proteins, Sialic Acids, Swine, Cell Culture Techniques, Mice
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