Animal-Free Human Whole Blood Sepsis Model to Study Changes in Innate ImmunityShow others and affiliations
2020 (English)In: Frontiers in Immunology, E-ISSN 1664-3224, Vol. 11, p. 1-12, article id 571992
Article in journal (Refereed) Published
Abstract [en]
Studying innate immunity in humans is crucial for understanding its role in the pathophysiology of systemic inflammation, particularly in the complex setting of sepsis. Therefore, we standardized a step-by-step process from the venipuncture to the transfer in a human model system, while closely monitoring the inflammatory response for up to three hours. We designed an animal-free, human whole blood sepsis model using a commercially available, simple to use, tubing system. First, we analyzed routine clinical parameters, including cell count and blood gas analysis. Second, we demonstrated that extracellular activation markers (e.g., CD11b and CD62l) as well as intracellular metabolic (intracellular pH) and functional (generation of radical oxygen species) features remained stable after incubation in the whole blood model. Third, we mimicked systemic inflammation during early sepsis by exposure of whole blood to pathogen-associated molecular patterns. Stimulation with lipopolysaccharide revealed the capability of the model system to evoke a sepsis-like inflammatory phenotype of innate immunity. In summary, the presented model serves as a convenient, economic, and reliable platform to study innate immunity in human whole blood, which may yield clinically important insights.
Place, publisher, year, edition, pages
Frontiers Media S.A., 2020. Vol. 11, p. 1-12, article id 571992
Keywords [en]
inflammation, neutrophil granulocytes, lipopolysaccharide (LPS), blood physiology, sepsis, ex vivo whole blood model, principles of the 3Rs
National Category
Immunology
Research subject
Biomedical Sciences, Immunology
Identifiers
URN: urn:nbn:se:lnu:diva-99888DOI: 10.3389/fimmu.2020.571992ISI: 000586896900001PubMedID: 33178198Scopus ID: 2-s2.0-85094665773OAI: oai:DiVA.org:lnu-99888DiVA, id: diva2:1517163
2021-01-132021-01-132024-01-17Bibliographically approved