Overlap of epitopes recognized by anti-carbonic anhydrase I IgG in patients with malignancy-related aplastic anemia-like syndrome and in patients with aplastic anemia
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23892086
DOI
10.1016/j.imlet.2013.07.006
PII: S0165-2478(13)00098-9
Knihovny.cz E-resources
- Keywords
- Anti-CA I autoantibodies, Aplastic anemia, Carbonic anhydrase I, Epitope extraction, LC–MS/MS,
- MeSH
- Anemia, Aplastic drug therapy immunology MeSH
- Autoantibodies blood immunology MeSH
- Epitopes immunology MeSH
- Immunoglobulin G immunology MeSH
- Carbonic Anhydrase I immunology MeSH
- Humans MeSH
- Epitope Mapping MeSH
- Neoplasms drug therapy immunology MeSH
- Stem Cell Transplantation adverse effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Autoantibodies MeSH
- Epitopes MeSH
- Immunoglobulin G MeSH
- Carbonic Anhydrase I MeSH
High titers of anti-carbonic anhydrase I (anti-CA I) autoantibodies were detected in the sera of patients with malignancies who developed an aplastic anemia-like (AA-like) syndrome after a high-dose therapy (HDT) and autologous stem cell transplantation (ASCT). It was found, that the presence of these anti-CA I autoantibodies is associated with spontaneous tumor regression. The main immunodominant epitopes of carbonic anhydrase isoform I (CA I) have previously been identified using epitope extraction technique in combination with mass spectrometric detection and bioinformatic verification. Similarly, the sera of patients with bona fide aplastic anemia (AA) who poorly responded to immunosuppressive treatment with anti-thymocyte globulin (ATG) demonstrated high titers of anti-CA I antibodies. In order to reveal differences between these antibodies, we applied the same methodology of epitope mapping procedure. Surprisingly, the anti-CA I antibodies from the both groups of patients compatibly recognized the same four candidate CA I epitopes--DGLAV, NVGHS, SLKPI, SSEQL. This finding may indicate common pathophysiological mechanisms in these two syndromes. However, at this moment it remains unresolved if anti-CA I antibodies are implicated in marrow or tumor suppression or are just an epi-phenomenon.
References provided by Crossref.org
Autoimmune phenomena and spontaneous tumour regression. The role of carbonic anhydrase I