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One or more keywords matched the following properties of Schreiber, Hans
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overview The main focus of this laboratory is to study the fundamental mechanisms that govern the interaction of cancer cells with the immune system. In particular, our laboratory is trying to exploit the fact that cancer cells usually carry cancer-specific mutations and antigens, and that under certain conditions, the immune system can destroy cancer cells even after they have disseminated in the body. We are trying to understand the mechanisms that often allow immunogenic cancer cells to escape immune destruction, and we want to develop new strategies and principles on which to base novel therapeutic approaches. We are also studying the signals needed for the immune system to be alerted be cancer cells, and then to destroy these cells. Finally, we combine immunology with genetics and biochemistry, which provides us with a powerful tool to search for cancer-specific changes in malignant cells in order to identify critical mechanisms and immunological targets that can be used to destroy the cancer.
One or more keywords matched the following items that are connected to Schreiber, Hans
Item TypeName
Concept Skin Window Technique
Concept Skin
Concept Transplantation Immunology
Concept Skin Neoplasms
Concept Skin Transplantation
Academic Article Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
Academic Article Antigenic cancer cells grow progressively in immune hosts without evidence for T cell exhaustion or systemic anergy.
Academic Article Ribosomal versus non-ribosomal cellular antigens: factors determining efficiency of indirect presentation to CD4+ T cells.
Academic Article Long-term inhibition of tumor growth by tumor necrosis factor in the absence of cachexia or T-cell immunity.
Academic Article Antigenic cancer cells that escape immune destruction are stimulated by host cells.
Academic Article Tumor antigens defined by cloned immunological probes are highly polymorphic and are not detected on autologous normal cells.
Academic Article Tumor necrosis factor/cachectin. Induction of hemorrhagic necrosis in normal tissue requires the fifth component of complement (C5).
Academic Article Animals bearing malignant grafts reject normal grafts that express through gene transfer the same antigen.
Academic Article Major histocompatibility complex class I and unique antigen expression by murine tumors that escaped from CD8+ T-cell-dependent surveillance.
Academic Article MHC-class I-restricted CD4 T cells: a nanomolar affinity TCR has improved anti-tumor efficacy in vivo compared to the micromolar wild-type TCR.
Academic Article [Clinical aspects and therapy of Merkel cell tumor--report of 4 personal cases and review of the literature].
Academic Article Editorial overview: tumour immunology.
Academic Article Adoptively transferred immune T cells eradicate established tumors despite cancer-induced immune suppression.
Grant Interdisciplinary Training Program in Immunology
Grant Immunology of Unique Tumor Specific Antigens
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  • skin
  • immunology