Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood
Basic science published in J Immunol (2021)
Abstract
Venous air embolism, which may complicate medical and surgical procedures, activates complement and triggers thromboinflammation. In lepirudin-anticoagulated human whole blood, we examined the effect of air bubbles on complement and its role in thromboinflammation. Whole blood from 16 donors was incubated with air bubbles without or with inhibitors of C3, C5, C5aR1, or CD14. Complement activation, hemostasis, and cytokine release were measured using ELISA and quantitative PCR. Compared with no air, incubating blood with air bubbles increased, on average, C3a 6.5-fold, C3bc 6-fold, C3bBbP 3.7-fold, C5a 4.6-fold, terminal complement complex sC5b9 3.6-fold, prothrombin fragments 1+2 (PTF1+2) 25-fold, tissue factor mRNA (TF-mRNA) 26-fold, microparticle tissue factor 6.1-fold, β-thromboglobulin 26-fold (all p < 0.05), and 25 cytokines 11-fold (range, 1.5-78-fold; all p < 0.0001). C3 inhibition attenuated complement and reduced PTF1+2 2-fold, TF-mRNA 5.4-fold, microparticle tissue factor 2-fold, and the 25 cytokines 2.7-fold (range, 1.4-4.9-fold; all p < 0.05). C5 inhibition reduced PTF1+2 2-fold and TF-mRNA 12-fold (all p < 0.05). C5 or CD14 inhibition alone reduced three cytokines, including IL-1β (p = 0.02 and p = 0.03). Combined C3 and CD14 inhibition reduced all cytokines 3.9-fold (range, 1.3-9.5-fold; p < 0.003) and was most pronounced for IL-1β (3.2- versus 6.4-fold), IL-6 (2.5- versus 9.3-fold), IL-8 (4.9- versus 8.6-fold), and IFN-γ (5- versus 9.5-fold). Antifoam activated complement and was avoided. PTF1+2 was generated in whole blood but not in plasma. In summary, air bubbles activated complement and triggered a C3-driven thromboinflammation. C3 inhibition reduced all mediators, whereas C5 inhibition reduced only TF-mRNA. Combined C5 and CD14 inhibition reduced IL-1β release. These data have implications for future mechanistic studies and possible pharmacological interventions in patients with air embolism.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Summary
Lepirudin-anticoagulated whole blood with air bubbles activates complement (C3a, C5a, sC5b9 etc.) and triggers C3-dependent thromboinflammation, with C3 inhibition reducing tissue factor and cytokine response.
Why This Matters for Hirudotherapy
This ex vivo study in human whole blood investigated how air bubbles trigger complement activation and C3-dependent thromboinflammation. The abstract notes that whole blood was anticoagulated with lepirudin to measure complement activation, hemostasis, and cytokine release. Lepirudin is known externally as a derivative of leech hirudin, but the abstract itself does not mention leeches, hirudotherapy, or the compound's origin. The abstract does not establish a link to hirudotherapy or the leech secretome. The study's actual focus is strictly on the mechanisms of venous air embolism and complement inhibition. Lepirudin is a recombinant derivative of hirudin, the anticoagulant of the medicinal leech (Greinacher, 2004); this paper studies the drug, not leech therapy.
Citation
Reference (Vancouver style)
Storm BS, Christiansen D, Fure H, Ludviksen JK, Lau C, Lambris JD, et al. Air Bubbles Activate Complement and Trigger Hemostasis and C3-Dependent Cytokine Release Ex Vivo in Human Whole Blood. J Immunol. 2021;207(11):2828-2840. doi:10.4049/jimmunol.2100308. PMID: 34732467
Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.
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