| Literature DB >> 32522835 |
Yajun Geng1,2, Gnanasekar Munirathinam1, Sunil Palani1, Joseph E Ross3, Bin Wang4, Aoshuang Chen5, Guoxing Zheng5.
Abstract
Extracellular high-mobility group box 1 (HMGB1) is a prototypic damage-associated molecular pattern. Although a homeostatic level of extracellular HMGB1 may be beneficial for immune defense, tissue repair, and tissue regeneration, excessive HMGB1 is linked to inflammatory diseases. This prompts an intriguing question: how does a healthy body control the level of extracellular HMGB1? In this study, in the plasma of both healthy humans and healthy mice, we have identified an anti-HMGB1 IgM autoantibody that neutralizes extracellular HMGB1 via binding specifically to a 100% conserved epitope, namely HMW4 (HMGB198-112). In mice, this anti-HMW4 IgM is produced by peritoneal B-1 cells, and concomitant triggering of their BCR and TLR4 by extracellular HMGB1 stimulates the production of anti-HMW4 IgM. The ability of extracellular HMGB1 to induce its own neutralizing Ab suggests a feedback loop limiting the level of this damage-associated molecular pattern in a healthy body.Entities:
Year: 2020 PMID: 32522835 PMCID: PMC7416627 DOI: 10.4049/jimmunol.2000014
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422