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The versatile functions of complement C3-derived ligands
Authors
Ahearn
Altieri
+151 more
Andrews
Arvieux
Aubry
Baiu
Bajtay
Bajtay
Barro
Baudino
Bellinger-Kawahara
Berger
Beyer
Bohnsack
Bretscher
Cabec
Cardone
Carroll
Carroll
Carroll
Carter
Carter
Castro
Chen
Chen
Colten
Corbi
Cravedi
Daha
Dempsey
Diamond
Ehirchiou
Erdei
Erdei
Erdei
Erdei
Erdei
Ezekowitz
Fearon
Fingeroth
Flick
Frade
Gadjeva
Georgakopoulos
Ghannam
Ghebrehiwet
Gros
Gupta
Han
Heeger
Helmy
Holers
Hynes
Iida
Illges
Ingalls
Isaak
Jacobson
Jozsi
Karnchanaphanurach
Kemper
Kerekes
Kerekes
Kerekov
Klos
Kooten
Kremlitzka
Kuraya
Kurtz
Law
Law
Li
Li
Liddington
Lu
Luxembourg
Maison
Marquart
Marquart
Matsumoto
Melchers
Miller
Miller
Mitchell
Mold
Molina
Morelli
Mueller-Ortiz
Nelson
Nemerow
Nicolaou
Nielsen
Ogembo
Olesen
Oliva
Pantazis
Papp
Patel
Pepys
Peyron
Pliyev
Postigo
Praz
Prechl
Prechl
Prieto
Prodeus
Puentes
Ramos
Raposo
Reis
Renzo
Ross
Rubtsov
Sacks
Sandor
Sandor
Schlesinger
Schmidt
Sim
Sim
Singh-Jasuja
Sissons
Skoberne
Sohn
Strainic
Strijp
Tan
Tedder
Thacker
Torok
Torok
Touw
Tsokos
Tsokos
Tsokos
Tuveson
Ueda
Ugarova
Verbovetski
Villiers
Wagner
Watry
Wehr
Weiss
White
Wilson
Wright
Yan
Zaffran
Zhang
Zhou
Zhou
Publication date
1 January 2016
Publisher
'Wiley'
Doi
Abstract
The complement system is a major component of immune defense. Activation of the complement cascade by foreign substances and altered self-structures may lead to the elimination of the activating agent, and during the enzymatic cascade, several biologically active fragments are generated. Most immune regulatory effects of complement are mediated by the activation products of C3, the central component. The indispensable role of C3 in opsonic phagocytosis as well as in the regulation of humoral immune response is known for long, while the involvement of complement in T-cell biology have been revealed in the past few years. In this review, we discuss the immune modulatory functions of C3-derived fragments focusing on their role in processes which have not been summarized so far. The importance of locally synthesized complement will receive special emphasis, as several immunological processes take place in tissues, where hepatocyte-derived complement components might not be available at high concentrations. We also aim to call the attention to important differences between human and mouse systems regarding C3-mediated processes. © 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Lt
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info:doi/10.1111%2Fimr.12498
Last time updated on 17/02/2019
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oai:real.mtak.hu:47319
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oai:edit.elte.hu:10831/75527
Last time updated on 28/08/2022