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The protective effect of modified intravenous immunoglobulin in LPS sepsis model is associated with an increased IRA B cells response
被引:19
作者:
Djoumerska-Alexieva, Iglika
[1
]
Pashova, Shina
[1
]
Vassilev, Tchavdar
[1
]
Pashov, Anastas
[1
]
机构:
[1] Bulgarian Acad Sci, Stefan Angelov Inst Microbiol, Dept Immunol, BU-1113 Sofia, Bulgaria
关键词:
Intravenous immunoglobulins;
B1;
lymphocytes;
CD93;
Innate response activator B1 cells;
Ferrous ions;
Sepsis;
ANTIGEN-BINDING;
DNA ANTIBODIES;
POLYREACTIVITY;
AUTOANTIBODIES;
EXPOSURE;
AGENTS;
TLR4;
IGG;
D O I:
10.1016/j.autrev.2012.10.010
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Intravenous immunoglobulin preparations (IVIg) that have undergone a mild oxidizing treatment with ferrous ions have an increased polyspecificity, which is not associated with a higher propensity to form aggregates. Among other biological properties of the modified IVIg, a protective effect in LPS sepsis model stands out as the native preparation is totally devoid of it or even exacerbates sepsis. A recent finding identified an LPS induced subset of B1 lymphocytes that migrate from the peritoneal cavity to the spleen acquiring the expression of CD93, GM-CSF as well as the capacity to control sepsis. This report demonstrates that modified IVIg, but not the native preparation, causes a further increase in this population during LPS sepsis. Partial targeted suppression of the peritoneal B cell proliferation by an intracellular dye abrogates this effect and the clinical benefit of modified IVIg. (C) 2012 Elsevier B.V. All rights reserved.
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页码:653 / 656
页数:4
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