Complement: An inflammatory pathway fulfilling multiple roles at the interface of innate immunity and development
Data
2005Soggetto
Abstract
Complement has been long perceived as an innate immune system that plays a pivotal role in the maintenance of host defense against infectious agents and the propagation of proinflammatory responses in the context of human disease. Complement activation has been associated with the onset of acute inflammatory reactions leading to complications such as acute graft rejection, local tissue injury and multiorgan failure. However, recent studies have indicated that various complement activation products may exert a beneficial effect by contributing to critical developmental and regenerative processes. Appreciating this extraordinary 'versatility' of complement proteins provides a framework for revisiting the design of effective complement therapeutics. A balanced strategy will have to consider limiting the detrimental proinflammatory effects of complement while preserving those activities that promote tissue repair and regeneration, cell survival and early development. © 2005 Bentham Science Publishers Ltd.
Collections
Related items
Showing items related by title, author, creator and subject.
-
Ascites in a patient with episodic angio-oedema and eosinophilia: Thinking outside the box
Rigopoulou E.I., Ioannou M., Papadamou G., Dalekos G.N. (2017)Episodic angio-oedema with eosinophilia (EAE) or Gleich's syndrome is a rare condition characterised by recurrent episodes of oedema and eosinophilia, accompanied by urticaria, fever and weight gain. The presence of ascites ... -
Deep Intronic SERPING1 Gene Variants: Ending One Odyssey and Starting Another?
Germenis A.E., Vatsiou S., Csuka D., Zamanakou M., Farkas H. (2021)[No abstract available] -
The Global Registry for Hereditary Angioedema due to C1-Inhibitor Deficiency
Zanichelli A., Farkas H., Bouillet L., Bara N., Germenis A.E., Psarros F., Varga L., Andrási N., Boccon-Gibod I., Castiglioni Roffia M., Rutkowski M., Cancian M. (2021)Hereditary angioedema (HAE) is a rare condition, mostly due to genetic deficiency of complement C1 inhibitor (C1-INH). The rarity of HAE impedes extensive data collection and assessment of the impact of certain factors ...