A monoclonal antibody against tumour necrosis factor alpha improves survival in experimental multiple organ dysfunction syndrome
Autor: | J.W.M. van der Meer, Thijs Hendriks, M.J.J.M. Jansen, R. Hermsen, R.J.A. Goris |
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Jazyk: | angličtina |
Rok vydání: | 1998 |
Předmět: |
Male
medicine.medical_specialty Pathology Necrosis medicine.drug_class The effect of modulation of endogenous cytokines on resistance to infection Multiple Organ Failure Immunology gastheer-parasiet interactie [Malaria] Modulation of macrophage sensitivity to inflammatory stimuli like endotoxin and zymosan parasite-host interaction [Malaria] Biology Tumour necrosis factor alpha Monoclonal antibody Biochemistry Mice chemistry.chemical_compound Internal medicine medicine Animals Immunology and Allergy Interleukin 6 Molecular Biology Lung Interleukin-6 Tumor Necrosis Factor-alpha Zymosan Antibodies Monoclonal Hematology medicine.disease Survival Analysis Het effect van modulatie van endogene cytokinen op weerstand tegen infecties Mice Inbred C57BL Organ damage Endocrinology medicine.anatomical_structure chemistry biology.protein medicine.symptom Modulatie van de sensitiviteit van macrofagen voor inflammatoire stimuli als endotoxine en zymosan Multiple organ dysfunction syndrome |
Zdroj: | Cytokine, 10, 904-910. W b saunders co Cytokine, 10, 904-910 Cytokine, 10, pp. 904-910 Cytokine, 10, 11, pp. 904-910 |
ISSN: | 1043-4666 |
Popis: | A single intraperitoneal administration of zymosan induces multiple organ dysfunction syndrome (MODS) in C57BL/6 mice. The authors investigated the effect of a monoclonal antibody V1q against murine tumour necrosis factor α (TNF-α) on the development of zymosan-induced MODS and on plasma concentrations and the production capacity of interleukin 6 (IL-6) by peritoneal cells. C57BL/6 mice received doses of V1q starting either simultaneously with administration of zymosan every four days, or from 4 or 8 days after administration of zymosan onwards. The animals were monitored for survival, condition, and body weight and temperature. Twelve days after zymosan all surviving animals were killed to obtain plasma, organs and peritoneal cells. Plasma concentrations of IL-6 and lipopolysaccharide-stimulated production of IL-6 by peritoneal cells were measured; organs were weighed as an indicator for organ damage and lung damage was assessed macroscopically. Survival improved when the animals were treated with V1q starting at either time point , and a subpopulation developed from the group receiving V1q from day 0 onwards that displayed improved body weight and temperature when compared to the animals receiving zymosan only. Also, the wet organ weights improved in this subgroup, indicating a beneficial effect of the monoclonal antibody. However, V1q administered could neither decrease the circulating IL-6 concentrations toward control values, nor did V1q treatment normalize IL-6 production capacity (stimulated or unstimulated). The development of zymosan-induced MODS can be attenuated by the monoclonal antibody V1q. |
Databáze: | OpenAIRE |
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