Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz
Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Paar, M; Fengler, VH; Schweiger, M; Rossmann, C; Nusshold, C; Mairold, M; Payerl, D; Cvirn, G; Oettl, K.
Albumin does not induce IL-6 release and toll-like receptor activation in vitro: Role of endotoxin contamination and biochemical modifications
BBA ADV. 2025; 8: 100174
Doi: 10.1016/j.bbadva.2025.100174
Web of Science
PubMed
FullText
FullText_MUG
- Führende Autor*innen der Med Uni Graz
- Öttl Karl
- Paar Margret
- Co-Autor*innen der Med Uni Graz
- Cvirn Gerhard
- Fengler Vera
- Mairold Martina
- Nusshold Christoph
- Payerl Doris
- Rossmann Christine Renate
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- Abstract:
- Human serum albumin (HSA) is widely used in both clinical and research settings, yet its potential to stimulate immune responses remains poorly understood. In this study, we systematically investigated various therapeutic, recombinant and plasma-derived albumin preparations for their ability to induce pro-inflammatory cytokine release by human peripheral blood mononuclear cells (PBMC) and activate Toll-like receptors (TLR) in HEKBlueTM TLR4 and TLR2 reporter cell lines. All albumin preparations were characterized in terms of their redox state of cysteine-34, glycation level, non-esterified fatty acid content, and endotoxin contamination Therapeutic albumin, as may be expected, did not induce IL-6-release nor TLR activation. However, several commercial research grade albumins, including fatty acid-free, glycated, and recombinant preparations, significantly induced IL-6 release and activated TLR4 and TLR2 signaling. These inflammatory effects were strongly correlated with the endotoxin content, while no consistent associations were found with albumin redox state, degree of glycation, or fatty acid load. Albumins with more reduced cysteine-34 content showed lower pro-inflammatory activity, but this correlation was lost when controlling for endotoxin levels, suggesting confounding by endotoxin contamination. Direct testing of isolated albumin redox fractions and in vitro glycated albumins confirmed that neither oxidation nor glycation of albumin, in the absence of endotoxin, triggered inflammatory responses in PBMCs. Inducing effects were found to be related to contaminating ligands and not to albumin itself. Our findings emphasize the need for rigorous product characterization and highlight the critical importance of endotoxin as a confounding factor in immune assays involving research grade albumin preparations.
- Find related publications in this database (Keywords)
- Human serum albumin
- Albumin redox state
- Glycated albumin
- Endotoxin contamination
- Cytokine release
- Toll-like receptors
- Inflammation