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Detection of autoantibodies against advanced glycation endproducts and AGE-immune complexes in serum of patients with diabetes mellitus
Abstract
Advanced glycation of protein causes their immunogenicity. The evidence that advanced glycation endproducts (AGEs) have antigenic properties has led to a hypothesis that the AGE structure found in vivo may exert an autoimmune response. In the present study, we showed the sera of diabetic patients as well as of nondiabetic individuals to contain autoantibodies to epitopes of AGE structures. Contrary to what might be expected, we observed lower AGE antibody titers in diabetic subjects, and postulated that the antibodies against AGEs form immune complexes in vivo, hampering their determination. The existence of immune complexes containing AGE moiety was established by two independent criteria: (a) serum AGE-immune complexes (AGE-IC) were detected by enzyme-linked immunosorbent assay (ELISA) using an immunochemical bridge; and (b) soluble AGE-IC were precipitated from serum by polyethylene glycol and analyzed. We demonstrated the presence of circulating AGE-IC in sera, predominantly in the sera of diabetic subjects. We also found an inverse correlation between serum AGE level and AGE-IC (r=-0.8, P<0.000), indicating the serum level of AGEs to decline with an increasing presence of AGE-IC. The content of AGE in soluble immune complexes was significantly higher in diabetic patients than in control subjects (3.51+/-1.9 vs. 1.89+/-1.0 microgEq/ml (P<0.00004), and correlated inversely with free antibodies (r=-0.26, P<0.01). Interactions of AGE autoantibodies with AGE as a continuously produced antigen result in the formation of AGE-immune complexes that may play a role in the atherogenic processes.
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“FoxO proteins are transcription factors which regulate the expression of genes involved in energy homeostasis, cell survival and inflammatory responses including NF-kB (274 -278) .”
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Azizah, N., Mashitah, M. W., & Samsu, N. (2018) · JURNAL Al-AZHAR INDONESIA SERI SAINS DAN TEKNOLOGI · doi:10.36722/sst.v4i3.283 · Cited by 1
Chauhan, S., Nath, N., Tule, V., & Tule, A. (2007) · International Journal of Diabetes in Developing Countries · doi:10.4103/0973-3930.37041 · Cited by 1
Oushah, H. (2026) · e-space (Manchester Metropolitan University) · doi:10.83056/mmu.32439042 · Cited by 1
Formation and inhibition of advanced glycation endproducts in meat and model systems
Chen, G. (2016) · K-State Research Exchange (Kansas State University) · Cited by 1
Aterosclerosis y trombosis en la diabetes mellitusNuevos aspectos de la fisiopatología
Colwell, J. A., Lyons, T. J., Klein, R. L., Lopes-Virella, M. E., & Jokl, R. (2008) · Elsevier eBooks · doi:10.1016/b978-84-8086-367-4.50005-9
Buettner, G. R., Oberley, L. W., Spitz, D. R., & Domann, F. E. (2003)
Metadata
- Authors
- Turk, Z., Ljubic, S., Turk, N., & Benko, B.
- Affiliations
- University of Zagreb (HR)
- Institute of Immunology (HR)
- Corresponding author
- Turk, Zdenka
- ORCID
- Turk, Nikša
- Venue
- Clinica Chimica Acta
- Publisher
- Elsevier BV
- Published
- 2001-01
- Volume
- 303
- Issue
- 1-2
- Pages
- 105-115
- ISSN
- 0009-8981 (ISSN-L)
- OpenAlex
- W2091966929
- Cited by
- 111
- References
- 21
- Citations by year
- 2026: 6 · 2025: 3 · 2024: 2 · 2023: 3 · 2022: 3 · 2021: 1 · 2020: 2 · 2019: 4 · 2018: 4 · 2017: 5 · 2016: 6 · 2015: 7 · 2014: 5 · 2013: 4 · 2012: 11
- FWCI
- 2.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinica Chimica Acta (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Health Sciences › Medicine › Dermatology › Skin Diseases and Diabetes
- Keywords
- advanced glycation end products, autoantibodies, diabetes mellitus, immune complex formation, atherosclerosis, polyethylene glycol precipitation
- MeSH terms
- Antigen-Antibody Complex, Autoantibodies, Diabetes Mellitus, Type 2, Enzyme-Linked Immunosorbent Assay, Humans, Glycation End Products, Advanced
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