Abstract |
Identification of new therapeutic targets for the treatment of sepsis is imperative. We report here that cytokine IL-28 (IFN-λ) levels were elevated in clinical and experimental sepsis. Neutralization of IL-28 protected mice from lethal sepsis induced by cecal ligation and puncture (CLP), which was associated with improved bacterial clearance and enhanced neutrophil infiltration. Conversely, administration of recombinant IL-28 aggravated mortality, facilitated bacterial dissimilation and limited neutrophil recruitment, in the model of sepsis induced by CLP. This study defines IL-28 as a detrimental mediator during sepsis and identifies a potential therapeutic target for the immune therapy in sepsis.
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Authors | Qin Luo, Yi Liu, Shuang Liu, Yibing Yin, Banglao Xu, Ju Cao |
Journal | Clinical immunology (Orlando, Fla.)
(Clin Immunol)
Vol. 205
Pg. 29-34
(08 2019)
ISSN: 1521-7035 [Electronic] United States |
PMID | 31121287
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2019 Elsevier Inc. All rights reserved. |
Chemical References |
- Antibodies, Neutralizing
- Cytokines
- interferon-lambda, human
- IL28A protein, mouse
- Interleukins
- interferon-lambda protein, mouse
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Topics |
- Adult
- Aged
- Animals
- Antibodies, Neutralizing
(pharmacology)
- Cecum
(surgery)
- Cytokines
(antagonists & inhibitors, pharmacology)
- Disease Models, Animal
- Female
- Humans
- Interleukins
(antagonists & inhibitors, immunology, pharmacology)
- Intestinal Perforation
- Male
- Mice
- Middle Aged
- Molecular Targeted Therapy
- Mortality
- Neutrophil Infiltration
(drug effects, immunology)
- Sepsis
(immunology)
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