期刊
CLINICAL AND EXPERIMENTAL IMMUNOLOGY
卷 121, 期 2, 页码 364-374出版社
WILEY
DOI: 10.1046/j.1365-2249.2000.01280.x
关键词
tRNP((Ser)Sec); UGA suppressor tRNA-protein complex; autoantibodies; autoantigen; autoimmune hepatitis
类别
We previously described autoantibodies against a UGA serine tRNA-protein complex (tRNP((Ser)Sec)) in patients with type-1 autoimmune hepatitis [1] and now define the specificity and frequency of this autoantibody and the DNA sequence encoding the tRNA((Ser)Sec)-associated antigenic protein. The presence of anti-tRNP((Ser)Sec) antibodies was highly specific for type-1 autoimmune hepatitis, as 47.5% of patients were positive compared with none of the control subjects. To characterize the antigenic protein(s), we immunoscreened a human cDNA library with anti-tRNP((Ser)Sec)-positive sera. Two clones (19 and 13) were isolated. Clone 19 encodes a protein with a predicted molecular mass of 48.8 kD. Clone 13 is a shorter cDNA, almost identical to clone 19, which encodes a 35.9-kD protein. Expression of both cDNAs was accomplished in Escherichia coli as His-tagged recombinant proteins. Antibodies eluted from both purified recombinant proteins were able to immunoprecipitate the tRNA((Ser)Sec) from a HeLa S-3 cell extract, demonstrating their cross-reactivity with the mammalian antigenic complex. Recent cloning data relating to the target antigen(s) of autoantibodies in autoimmune hepatitis patients that react with a soluble liver antigen (SLA) and a liver-pancreas antigen (LP) have revealed that these two autoantibodies are identical and that the cloned antigen shows 99% amino acid sequence homology with tRNP((Ser)Sec).
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