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
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