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Identifizierung von Zielantigenen für Antikörper und T-Zellen

Identification of target antigens for antibodies and T cells

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Zusammenfassung

Grundsätzlich eignen sich alle Proteine mit spezifischer oder überwiegender Expression in Tumorgewebe als Zielstrukturen aktiver bzw. passiver immuntherapeutischer Strategien. Die klinischen Erfolge der letzten Jahre ermutigen die Forschung zur Identifizierung neuer Zielstrukturen. Geeignete Kandidaten sind neben tumoreigenen Proteinen auch solche, die vom Tumorstroma mit hoher Spezifität und Selektivität überexprimiert werden. Dazu gehören z. B. Wachstumsfaktoren, extrazelluläre Matrixproteine und Zelloberflächenproteine neu gebildeter Tumorgefäße. Die Suche nach Kandidatenantigenen erfolgte zunächst mit vorab generierten antitumoralen Antikörpern bzw. T-Zellen, mittlerweile aber überwiegend mit molekularbiologischen und proteinchemischen Hochdurchsatz-Screeningverfahren sowie Datenbankanalysen. Die präklinische Validierung der Kandidatenantigene umfasst neben Untersuchungen zur Verteilung, Homogenität und Stärke ihrer Expression auch die Analyse ihrer funktionellen Bedeutung und – insbesondere für Vakzinierungsstrategien – ihrer tatsächlichen Immunogenität.

Abstract

In principal, all proteins specifically or preferentially expressed in tumor tissues can be regarded as target candidates for active or passive immunotherapy strategies. Clinical success achieved in the past years promotes the identification of new target structures. Aside from proteins expressed by the tumor itself also proteins overexpressed by stromal cells are regarded as suitable candidates. Among the latter are e.g. growth factors, extracellular matrix proteins and cell surface proteins of the tumor neovasculature. The search for candidate target antigens originally depended on the availability of anti-tumor antibodies or T cells, respectively. But in the meantime genomic and proteomic high-throughput screening techniques and data mining procedures clearly dominate. The preclinical validation of candidate antigens includes expression profiling as well as analyses on their functional relevance and – especially for vaccine candidates – their immunogenicity.

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Literatur

  1. Rosenberg SA (2004) Shedding light on immunotherapy for cancer. N Engl J Med 350:1461–1463

    Google Scholar 

  2. Carter P, Smith L, Ryan M (2004) Identification and validation of cell surface antigens for antibody targeting in oncology. Endocr Relat Cancer 11:659–687

    Google Scholar 

  3. Rammensee HG, Falk K, Rötzschke O (1993) MHC molecules as peptide receptors. Curr Opin Immunol 5:35–44

    Google Scholar 

  4. Wölfel T, Hauer M, Schneider J et al. (1995) A p16INK4a-insensitive CDK4 mutant targeted by cytolytic T lymphocytes in a human melanoma. Science 269:1281–1284

    Google Scholar 

  5. Crotzer VL, Christian RE, Brooks JM et al. (2000) Immunodominance among EBV-derived epitopes restricted by HLA-B27 does not correlate with epitope abundance in EBV-transformed B-lymphoblastoid cell lines. J Immunol 164:6120–6129

    Google Scholar 

  6. Robbins PF, El-Gamil M, Li YF et al. (1996) A mutated ß-catenin gene encodes a melanoma-specific antigen recognized by tumor infiltrating lymphocytes. J Exp Med 183:1185–1192

    Google Scholar 

  7. Sharkey MS, Lizee G, Gonzales MI et al. (2004) CD4(+) T-cell recognition of mutated B-RAF in melanoma patients harboring the V599E mutation. Cancer Res 64:1595–1599

    Google Scholar 

  8. Mendelsohn J, Baselga J (2003) Status of epidermal growth factor receptor antagonists in the biology and treatment of cancer. J Clin Oncol 21:2787–2799

    Google Scholar 

  9. Parikh AA, Ellis LM (2004) The vascular endothelial growth factor family and its receptors. Hematol Oncol Clin North Am 18:951–971

    Google Scholar 

  10. Maecker B, von Bergwelt-Baildon M, Anderson KS et al. (2001) Linking genomics to immunotherapy by reverse immunology--’immunomics‘ in the new millennium. Curr Mol Med 1:609–619

    Google Scholar 

  11. Türeci Ö, Ding J, Hilton H et al. (2003) Computational dissection of tissue contamination for identification of colon cancer-specific expression profiles. Faseb J 17:376–385

    Google Scholar 

  12. Flower DR, McSparron H, Blythe MJ et al. (2003) Computational vaccinology: quantitative approaches. Novartis Found Symp 254:102–120; discussion 120–125, 216–222, 250–252

    Google Scholar 

  13. Wikstrand CJ, Hale LP, Batra SK et al. (1995) Monoclonal antibodies against EGFRvIII are tumor specific and react with breast and lung carcinomas and malignant gliomas. Cancer Res 55:3140–3148

    Google Scholar 

  14. Skipper JC, Hendrickson RC, Gulden PH et al. (1996) An HLA-A2-restricted tyrosinase antigen on melanoma cells resulted from posttranslational modification and suggests a novel pathway for processing of membrane proteins. J Exp Med 183:527–534

    Google Scholar 

  15. Sahin U, Türeci Ö, Pfreundschuh M (1997) Serological identification of human tumor antigens. Curr Opin Oncol 9:709–716

    Google Scholar 

  16. De Plaen E, Lurquin C, Brichard V et al. (1997) Cloning of genes coding for antigens recognized by cytolytic T lymphocytes. Immunology Methods Manual, Academic Press Ltd. 692–718

  17. Kruger T, Schoor O, Lemmel C et al. (2004) Lessons to be learned from primary renal cell carcinomas: novel tumor antigens and HLA ligands for immunotherapy. Cancer Immunol Immunother, Epub ahead of print

    Google Scholar 

  18. Lemmel C, Weik S, Eberle U et al. (2004) Differential quantitative analysis of MHC ligands by mass spectrometry using stable isotope labeling. Nat Biotechnol 22:450–454

    Google Scholar 

  19. Coulie PG, Ikeda H, Baurein JF, Chiari R (1999) Antitumor immunity at work in a melanoma patient. Adv Cancer Res 76:213–242

    Google Scholar 

  20. Robbins PF, El-Gamil M, Li YF et al. (2002) Multiple HLA class II-restricted melanocyte differentiation antigens are recognized by tumor-infiltrating lymphocytes from a patient with melanoma. J Immunol 169:6036–6047

    Google Scholar 

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Wölfel, T. Identifizierung von Zielantigenen für Antikörper und T-Zellen. Onkologe 11, 489–493 (2005). https://doi.org/10.1007/s00761-005-0871-z

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