Her main research concerns Immunology, Immune system, Antigen, CTL* and Molecular biology. Her Immunology research integrates issues from Cancer research, Cell therapy and Graft-versus-host disease. Catia Traversari combines subjects such as Apoptosis, Cell biology and Suicide gene with her study of Immune system.
Her work in Antigen is not limited to one particular discipline; it also encompasses Melanoma-Specific Antigens. Her CTL* research is multidisciplinary, relying on both Human leukocyte antigen, T lymphocyte, Melanoma and Virology. Her Molecular biology study combines topics in areas such as TBX1 and Gene.
Catia Traversari mainly investigates Immunology, Antigen, Molecular biology, Cancer research and Immune system. Her Immunology study incorporates themes from Hematopoietic stem cell transplantation and Suicide gene. Her Antigen study combines topics from a wide range of disciplines, such as Cytotoxic T cell, Melanoma and Gene, Transfection.
The various areas that Catia Traversari examines in her Molecular biology study include Human leukocyte antigen, Nucleic acid, Tumor rejection antigen and Cytolysis. Catia Traversari has researched Cancer research in several fields, including Tumor necrosis factor alpha, Cancer and Lewis lung carcinoma. In Immune system, Catia Traversari works on issues like Cell biology, which are connected to Innate immune system, Cell and Cell growth.
Her primary areas of investigation include Immunology, Cancer research, Immune system, Suicide gene and Cell biology. Catia Traversari regularly ties together related areas like Cytotoxic T cell in her Immunology studies. The concepts of her Cancer research study are interwoven with issues in Carcinogenesis, Vascular-targeting agent, Peptide and Immunotherapy.
The CXC chemokine receptors research she does as part of her general Immune system study is frequently linked to other disciplines of science, such as Oxysterol and Liver X receptor, therefore creating a link between diverse domains of science. Her research in Suicide gene intersects with topics in CD44 and CD8, Antigen. Catia Traversari combines topics linked to Tumor antigen with her work on Antigen.
Immunology, Immune system, Oxysterol, Liver X receptor and Cancer research are her primary areas of study. Her work on T cell, Active immunotherapy and Antigen as part of general Immunology research is frequently linked to Neurotoxicity, thereby connecting diverse disciplines of science. Catia Traversari interconnects Melanoma and Vaccination in the investigation of issues within Immune system.
Her study in Cancer research is interdisciplinary in nature, drawing from both Neuroendocrine tumors, Cell sorting, Monoclonal antibody and Immunotherapy. Her Immunotherapy study incorporates themes from Marker gene, CD44, CD19 and Suicide gene. Her study in Cell biology is interdisciplinary in nature, drawing from both Dendritic cell migration, Chemotaxis, CXC chemokine receptors and Cell growth.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma
P van der Bruggen;C Traversari;P Chomez;C Lurquin.
Science (1991)
HSV-TK Gene Transfer into Donor Lymphocytes for Control of Allogeneic Graft-Versus-Leukemia
Chiara Bonini;Giuliana Ferrari;Simona Verzeletti;Paolo Servida.
Science (1997)
A new gene coding for a differentiation antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas
P G Coulie;V Brichard;A Van Pel;T Wölfel.
Journal of Experimental Medicine (1994)
Structure, Chromosomal Localization, and Expression of 12 Genes of the Mage Family
Etienne De Plaen;Etienne De Plaen;Catia Traversari;Catia Traversari;José J.J. Gaforio;José J.J. Gaforio;Jean Pierre Szikora;Jean Pierre Szikora.
Immunogenetics (1994)
A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E.
C Traversari;P van der Bruggen;I F Luescher;C Lurquin.
Journal of Experimental Medicine (1992)
Monocyte-derived IL-1 and IL-6 are differentially required for cytokine-release syndrome and neurotoxicity due to CAR T cells
Margherita Norelli;Barbara Camisa;Giulia Barbiera;Laura Falcone.
Nature Medicine (2018)
HMGB1 is an endogenous immune adjuvant released by necrotic cells
Patrizia Rovere-Querini;Annalisa Capobianco;Paola Scaffidi;Barbara Valentinis.
EMBO Reports (2004)
Differentiation of T Regulatory Cells by Immature Dendritic Cells
Maria Grazia Roncarolo;Megan K. Levings;Catia Traversari.
Journal of Experimental Medicine (2001)
A peptide encoded by human gene MAGE-3 and presented by HLA-A2 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE-3.
P van der Bruggen;J Bastin;T Gajewski;T Gajewski;P G Coulie.
European Journal of Immunology (1994)
Infusion of suicide-gene-engineered donor lymphocytes after family haploidentical haemopoietic stem-cell transplantation for leukaemia (the TK007 trial): a non-randomised phase I–II study
Fabio Ciceri;Chiara Bonini;Maria Teresa Lupo Stanghellini;Attilio Bondanza.
Lancet Oncology (2009)
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