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Secretion and Immunogenicity of the Meningioma-Associated Antigen TXNDC16
Author(s) -
Christian Harz,
Nicole Ludwig,
Sven Lang,
Tamara V. Werner,
Valentina Galata,
Christina Backes,
Katja Schmitt,
Ruth M. Nickels,
Elmar Krause,
Martin Jung,
Jens Rettig,
Andreas Keller,
M. D. Menger,
Richard Zimmermann,
Eckart Meese
Publication year - 2014
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1303098
Subject(s) - secretion , immunogenicity , autoantibody , epitope , antigen , meningioma , flow cytometry , glycoprotein , microbiology and biotechnology , endoplasmic reticulum , biology , immune system , immunology , antibody , chemistry , medicine , biochemistry , pathology
In a previous study, we identified thioredoxin domain containing 16 (TXNDC16) as a meningioma-associated Ag by protein macroarray screening. Serological screening detected autoantibodies against TXNDC16 exclusively in meningioma patients' sera and not in sera of healthy controls. TXNDC16 was previously found to be an endoplasmic reticulum (ER)-luminal glycoprotein. In this study, we show an additional ER-associated localization of TXNDC16 in the cytosol by in vitro synthesis, molecular mass shift assay, and flow cytometry. We were able to show TXNDC16 secretion in different human cell lines due to masked and therefore nonfunctional ER retrieval motif. A previously indicated exosomal TXNDC16 secretion could not be confirmed in HEK293 cells. The secreted serum protein TXNDC16 is bound in circulating immune complexes, which were found both in meningioma and healthy blood donor sera. Employing a customized array with 163 overlapping TXNDC16 peptides and measuring autoantibody reactivity, we achieved discrimination of meningioma sera from healthy controls with an accuracy of 87.2% using a set of only five immunogenic TXNDC16 epitopes.

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