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The Clinical Significance of IgA Antimitochondrial Antibodies in Sera and Saliva in Primary Biliary Cirrhosis
Author(s) -
TANAKA ATSUSHI,
NEZU SAEKO,
UEGAKI SATOKO,
MIKAMI MASAKI,
OKUYAMA SHUHEI,
KAWAMURA NAOHIRO,
AISO MITSUHIKO,
GERSHWIN M. ERIC,
TAKAHASHI SHINICHI,
SELMI CARLO,
TAKIKAWA HAJIME
Publication year - 2007
Publication title -
annals of the new york academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.712
H-Index - 248
eISSN - 1749-6632
pISSN - 0077-8923
DOI - 10.1196/annals.1381.028
Subject(s) - saliva , primary biliary cirrhosis , autoantibody , medicine , immunoglobulin a , immunology , antibody , immunoglobulin g
 It still remains unclear how antimitochondrial autoantibodies (AMA) are involved with immunopathogenesis of primary biliary cirrhosis (PBC). We have suggested the potential role of IgA‐AMA in damage to epithelial cells in PBC. In the current study, we investigated whether IgA‐AMA were detectable in sera and saliva of PBC patients, to examine the association between detectable IgA‐type autoantibodies in sera or saliva and progression of liver diseases. Fifty‐three patients with PBC were enrolled, and IgA‐AMA in sera and saliva were sought by immunoblotting using pork heart mitochondria as antigens. The progression of PBC was determined as Scheuer's classification consisting of four histological stages. We found IgA‐AMA, IgA‐anti‐PDC‐E2, and IgA‐anti‐E3BP in 43/53 (81%), 37/53 (70%), and 35/53 (66%) sera of patients with PBC, but none of controls. The progression of PBC was statistically associated with presence of IgA‐anti‐PDC‐E2 ( P = 0.0124), but neither with IgA‐AMA ( P = 0.1296) nor anti‐IgA‐E3BP ( P = 0.5973). In saliva, detectable IgA‐AMA, IgA‐anti‐PDC‐E2, and IgA‐anti‐E3BP were noted in 12/26 (46%), 6/26 (23%), and 11/26 (42%), respectively. Detection of IgA‐anti‐PDC‐E2 was strongly associated with progression of PBC ( P = 0.0002), whereas detection of IgA‐AMA and IgA‐anti‐E3BP were not associated ( P = 0.2145 and P = 0.5118). The current findings suggest that the presence of IgA‐anti‐PDC‐E2 in sera or saliva might be associated with progression of PBC, although a prospective study with PBC patients with detectable IgA‐anti‐PDC‐E2 at early stages will be required to conclude the contribution of IgA‐anti‐PDC‐E2 to the progression of PBC.

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