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Verfasst von:Shraibman, Bracha [VerfasserIn]   i
 Wick, Wolfgang [VerfasserIn]   i
 Platten, Michael [VerfasserIn]   i
 Winkler, Frank [VerfasserIn]   i
 Deimling, Andreas von [VerfasserIn]   i
Titel:Identification of tumor antigens among the HLA peptidomes of glioblastoma tumors and plasma
Verf.angabe:Bracha Shraibman, Eilon Barnea, Dganit Melamed Kadosh, Yael Haimovich, Gleb Slobodin, Itzhak Rosner, Carlos López-Larrea, Norbert Hilf, Sabrina Kuttruff, Colette Song, Cedrik Britten, John Castle, Sebastian Kreiter, Katrin Frenzel, Marcos Tatagiba, Ghazaleh Tabatabai, Pierre-Yves Dietrich, Valérie Dutoit, Wolfgang Wick, Michael Platten, Frank Winkler, Andreas von Deimling, Judith Kroep, Juan Sahuquillo, Francisco Martinez-Ricarte, Jordi Rodon, Ulrik Lassen, Christian Ottensmeier, Sjoerd H. van der Burg, Per Thor Straten, Hans Skovgaard Poulsen, Berta Ponsati, Hideho Okada, Hans-Georg Rammensee, Ugur Sahin, Harpreet Singh, and Arie Admon
E-Jahr:2018
Jahr:August 2, 2018
Umfang:14 S.
Fussnoten:This article has been retracted ; Gesehen am 18.09.2019
Titel Quelle:Enthalten in: Molecular & cellular proteomics
Ort Quelle:Bethesda, Md. : The American Society for Biochemistry and Molecular Biology, 2002
Jahr Quelle:2018
Band/Heft Quelle:17(2018), 11, Seite 2132-2145
ISSN Quelle:1535-9484
Abstract:Glioblastoma multiforme (GBM) is the most aggressive brain tumor with poor prognosis to most patients. Immunotherapy of GBM is a potentially beneficial treatment option, whose optimal implementation may depend on familiarity with tumor specific antigens, presented as HLA peptides by the GBM cells. Furthermore, early detection of GBM, such as by a routine blood test, may improve survival, even with the current treatment modalities. This study includes large-scale analyses of the HLA peptidome (immunopeptidome) of the plasma-soluble HLA molecules (sHLA) of 142 plasma samples, and the membranal HLA of GBM tumors of 10 of these patients' tumor samples. Tumor samples were fresh-frozen immediately after surgery and the plasma samples were collected before, and at multiple visits after surgery. In total, this HLA peptidome analysis involved 52 different HLA allotypes and resulted in the identification of more than 35,000 different HLA peptides. Strong correlations were observed in the signal intensities and in the repertoires of identified peptides between the tumors and plasma-soluble HLA peptidomes of the individual patients, whereas low correlations were observed between these HLA peptidomes and the tumors' proteomes. HLA peptides derived from Cancer/Testis Antigens (CTAs) were selected based on their presence among the HLA peptidomes of the patients and absence of expression of their source genes from any healthy and essential human tissues, except from immune-privileged sites. Additionally, peptides were selected as potential biomarkers if their levels in the plasma-sHLA peptidome were significantly reduced after the removal of tumor mass. The CTAs identified among the analyzed HLA peptidomes provide new opportunities for personalized immunotherapy and for early diagnosis of GBM.
DOI:doi:10.1074/mcp.RA118.000792
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: http://dx.doi.org/10.1074/mcp.RA118.000792
 DOI: https://doi.org/10.1074/mcp.RA118.000792
Datenträger:Online-Ressource
Sprache:eng
Bibliogr. Hinweis:Errata: Shraibman, Bracha: Withdrawal
Sach-SW:Alleles
 Amino Acid Sequence
 Antigens, Neoplasm
 Biomarkers, Tumor
 Cancer biomarker(s)
 Cancer therapeutics
 Cell Membrane
 CTA - cancer/testis antigens
 Glioblastoma
 HLA - human leukocytes antigen
 HLA Antigens
 Humans
 Immunoaffinity
 Immunology
 immunotherapy
 MHC - major histocompatibility complex
 Peptides
 Peptidomics
 Plasma or serum analysis
 Proteome
 Solubility
K10plus-PPN:1677276908
Verknüpfungen:→ Zeitschrift

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