Publication | Open Access
A novel Mutein of TNFα Containing the Arg‐Gly‐Asp Sequence Shows Reduced Toxicity in Intestine
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Citations
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References
1994
Year
Gastrointestinal PharmacologyCell AdhesionImmunologyGastroenterologyCell DeathPathologyImmune RegulationGastrointestinal Peptide HormoneInflammationNovel MuteinCell SignalingAllergyChronic InflammationVascular BiologyTnfalpha MoleculeTumor MicroenvironmentAnti-inflammatoryPathogenesisEndothelial DysfunctionEnhanced AdhesionWound HealingTnfalpha InjectionMedicineExtracellular Matrix
The effects of human tumour necrosis factor-alpha (TNFalpha), or its mutein (F4168) having the cell adhesive Arg-Gly-Asp sequence at the N-terminus, on intestinal injury, were examined. Histopathological examination revealed that an intravenous injection of TNFalpha resulted in marked haemorrhage or oedema in the caecum of rats, whereas F4168 showed no such effects even at the same therapeutic dose. Moreover, the number of neutrophils that adhered to endothelial cells or infiltrated the mucosal tissue was much higher after TNFalpha injection compared with F4168 in vivo. The enhanced adhesion of neutrophils on to human umbilical vein endothelial cells also occurred when the latter were pre-stimulated with TNFalpha but not with F4168 in vitro. The expression of the cell adhesion molecules including endothelial leukocyte adhesion molecule-1 or intercellular adhesion molecule-1 on F4168- stimulated human umbilical vein endothelial ceils was significantly lower than that stimulated with TNFalpha. These results suggest that the Arg-Gly-Asp sequence introduced into the TNFalpha molecule abrogates the side effect of this cytokine such as tissue injury or shock, and that F4168 could be useful for systemic therapy.
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