Somatic Mutations Modulate Autoantibodies against Galactose-Deficient IgA1 in IgA Nephropathy
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
P30 AI027767
NIAID NIH HHS - United States
R01 GM098539
NIGMS NIH HHS - United States
K01 DK106341
NIDDK NIH HHS - United States
P30 CA013148
NCI NIH HHS - United States
R01 DK078244
NIDDK NIH HHS - United States
F31 DK109599
NIDDK NIH HHS - United States
U01 HG008680
NHGRI NIH HHS - United States
R01 DK082753
NIDDK NIH HHS - United States
T32 GM008111
NIGMS NIH HHS - United States
R56 DK078244
NIDDK NIH HHS - United States
PubMed
26966014
PubMed Central
PMC5084875
DOI
10.1681/asn.2014101044
PII: ASN.2014101044
Knihovny.cz E-zdroje
- Klíčová slova
- IgA nephropathy, immune complexes, immunology,
- MeSH
- autoprotilátky genetika MeSH
- galaktosa nedostatek MeSH
- IgA nefropatie enzymologie genetika imunologie MeSH
- imunoglobulin A * MeSH
- lidé MeSH
- mutace * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- autoprotilátky MeSH
- galaktosa MeSH
- imunoglobulin A * MeSH
Autoantibodies against galactose-deficient IgA1 drive formation of pathogenic immune complexes in IgA nephropathy. IgG autoantibodies against galactose-deficient IgA1 in patients with IgA nephropathy have a specific amino-acid sequence, Y1CS3, in the complementarity-determining region 3 of the heavy chain variable region compared with a Y1CA3 sequence in similar isotype-matched IgG from healthy controls. We previously found that the S3 residue is critical for binding galactose-deficient IgA1. To determine whether this difference is due to a rare germline sequence, we amplified and sequenced the corresponding germline variable region genes from peripheral blood mononuclear cells of seven patients with IgA nephropathy and six healthy controls from whom we had cloned single-cell lines secreting monoclonal IgG specific for galactose-deficient IgA1. Sanger DNA sequencing revealed that complementarity-determining region 3 in the variable region of the germline genes encoded the Y1C(A/V)3 amino-acid sequence. Thus, the A/V>S substitution in the complementarity-determining region 3 of anti-galactose-deficient-IgA1 autoantibodies of the patients with IgA nephropathy is not a rare germline gene variant. Modeling analyses indicated that the S3 hydroxyl group spans the complementarity-determining region 3 loop stem, stabilizing the adjacent β-sheet and stem structure, important features for effective binding to galactose-deficient IgA1. Understanding processes leading to production of the autoantibodies may offer new approaches to treat IgA nephropathy.
Columbia University New York New York
Juntendo University Faculty of Medicine Tokyo Japan
Palacky University and University Hospital Olomouc Olomouc Czech Republic
University of Alabama at Birmingham Birmingham Alabama
University of Alabama at Birmingham Birmingham Alabama;
University of Nebraska Medical Center Omaha Nebraska
University of Tennessee Health Science Center Memphis Tennessee; and
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