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Sökning: id:"swepub:oai:DiVA.org:lnu-85855" > C3-Glomerulopathy A...

C3-Glomerulopathy Autoantibodies Mediate Distinct Effects on Complement C3-and C5-Convertases

Zhao, Fei (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
Afonso, Sara (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
Lindner, Susanne (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
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Hartmann, Andrea (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
Loeschmann, Ina (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
Nilsson, Bo (författare)
Uppsala universitet,Klinisk immunologi
Nilsson Ekdahl, Kristina (författare)
Linnéuniversitetet,Institutionen för kemi och biomedicin (KOB),Linnaeus Ctr Biomat Chem, BMC,Linnaeus Univ, Linneaus Ctr Bomat Chem, Kalmar, Sweden
Weber, Lutz T. (författare)
Univ Hosp Cologne, Childrens & Adolescents Hosp Cologne, Cologne, Germany
Habbig, Sandra (författare)
Univ Hosp Cologne, Childrens & Adolescents Hosp Cologne, Cologne, Germany
Schalk, Gesa (författare)
Univ Hosp Cologne, Childrens & Adolescents Hosp Cologne, Cologne, Germany
Kirschfink, Michael (författare)
Heidelberg Univ, Inst Immunol, Heidelberg, Germany
Zipfel, Peter F. (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany;Friedrich Schiller Univ Jena, Fac Life Sci, Jena, Germany
Skerka, Christine (författare)
Leibniz Inst Nat Prod Res & Infect Biol, Deparment Infect Biol, Jena, Germany
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 (creator_code:org_t)
2019-05-31
2019
Engelska.
Ingår i: Frontiers in Immunology. - : Frontiers Media S.A.. - 1664-3224. ; 10, s. 1-14
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • C3 glomerulopathy (C3G) is a severe kidney disease, which is caused by defective regulation of the alternative complement pathway. Disease pathogenesis is heterogeneous and is caused by both autoimmune and genetic factors. Here we characterized IgG autoantibodies derived from 33 patients with autoimmune C3 glomerulopathy. Serum antibodies from all 33 patients as well as purified IgGs bound to the in vitro assembled C3-convertase. Noteworthy, two groups of antibodies were identified: group 1 with strong (12 patients) and group 2 with weak binding C3-convertase autoantibodies (22 patients). C3Nef, as evaluated in a standard C3Nef assay, was identified in serum from 19 patients, which included patients from group 1 as well as group 2. The C3-convertase binding profile was independent of C3Nef. Group 1 antibodies, but not the group 2 antibodies stabilized the C3-convertase, and protected the enzyme from dissociation by Factor H. Also, only group 1 antibodies induced C3a release. However, both group 1 and group 2 autoantibodies bound to the C5-convertase and induced C5a generation, which was inhibited by monoclonal anti-C5 antibody Eculizumab in vitro. In summary, group 1 antibodies are composed of C3Nef and C5Nef antibodies and likely over-activate the complement system, as seen in hemolytic assays. Group 2 antibodies show predominantly C5Nef like activities and stabilize the C5 but not the C3-convertase. Altogether, these different profiles not only reveal a heterogeneity of the autoimmune forms of C3G (MPGN), they also show that in diagnosis of C3G not all autoimmune forms are identified and thus more vigorous autoantibody testing should be performed.

Ämnesord

NATURVETENSKAP  -- Biologi -- Immunologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Immunology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Nyckelord

C3 glomerulopathy
C3NeF
C5Nef
complement
Eculizumab
Immunologi
Immunology

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