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Gewählte Publikation:

Schrama, D; Straten, PT; Fischer, WH; McLellan, AD; Brocker, EB; Reisfeld, RA; Becker, JC.
Targeting of lymphotoxin-alpha to the tumor elicits an efficient immune response associated with induction of peripheral lymphoid-like tissue
IMMUNITY. 2001; 14(2): 111-121. Doi: 10.1016/S1074-7613(01)00094-2 [OPEN ACCESS]
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Führende Autor*innen der Med Uni Graz
Becker Jürgen Christian
Schrama David
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Abstract:
A recombinant antibody-lymphotoxin-alpha fusion protein induced an adaptive immune response protecting mice from melanoma. Importantly, this fusion protein elicited the formation of a lymphoid-like tissue in the tumor microenvironment containing L-selectin+ T cells and MHC class II+ antigen-presenting cells, as well as B and T cell aggregates. Furthermore, PNAd+/TCA4+ high endothelial venules were observed within the tumor, suggesting entry channels for naive T cell infiltrates. Over the course of therapy, a marked clonal expansion of certain TCR specificities occurred among tumor-infiltrating lymphocytes that displayed reactivity against melanoma cells and the TRP-2(180-188) peptide. Consequently, naive T cells may have been recruited to as well as primed and expanded in the lymphoid-like tissue induced by the lymphotoxin-alpha fusion protein at the tumor site.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Antibodies, Monoclonal - therapeutic use
Endothelium, Lymphatic - immunology Endothelium, Lymphatic - pathology
Humans -
Immunotoxins - therapeutic use
Lung Neoplasms - immunology Lung Neoplasms - secondary Lung Neoplasms - therapy
Lymphocytes, Tumor-Infiltrating - immunology Lymphocytes, Tumor-Infiltrating - pathology
Lymphoid Tissue - immunology Lymphoid Tissue - pathology
Lymphotoxin-alpha - therapeutic use
Melanoma, Experimental - immunology Melanoma, Experimental - pathology Melanoma, Experimental - therapy
Mice -
Mice, Inbred C57BL -
Microscopy, Electron -
Neoplasm Transplantation -
Neoplasms, Connective Tissue - immunology Neoplasms, Connective Tissue - pathology Neoplasms, Connective Tissue - therapy
Recombinant Fusion Proteins - therapeutic use
T-Lymphocytes - immunology T-Lymphocytes - pathology
Transplantation, Isogeneic -

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