Her primary scientific interests are in Cell biology, T cell, CD28, Immunology and Cytotoxic T cell. Her biological study spans a wide range of topics, including Interleukin 2, Receptor, IL-2 receptor and Immune tolerance. She is involved in the study of T cell that focuses on T-cell receptor in particular.
Her CD28 research incorporates themes from Ex vivo, CD86, Immunosuppression, CD80 and Antigen presentation. In Immunology, Vassiliki A. Boussiotis works on issues like In vivo, which are connected to Tuberculosis, Mycobacterium tuberculosis, Interferon gamma, Interleukin 10 and In vitro. Her work is dedicated to discovering how Cytotoxic T cell, Molecular biology are connected with FYN, CRKL, Semaphorin, CD72 and Germinal center and other disciplines.
Vassiliki A. Boussiotis spends much of her time researching Cell biology, T cell, Immunology, Immune system and Cancer research. Her research in Cell biology intersects with topics in Receptor, Jurkat cells and T-cell receptor. Vassiliki A. Boussiotis has researched T cell in several fields, including Cytotoxic T cell and Cell cycle.
The concepts of her Immunology study are interwoven with issues in Hematopoietic stem cell transplantation, Stem cell and Transplantation. Her studies deal with areas such as Transcription factor, B cell and Effector as well as Immune system. The Cancer research study which covers Immunotherapy that intersects with Tumor microenvironment.
Her main research concerns Cell biology, T cell, Cancer research, Immune system and Immunology. Vassiliki A. Boussiotis studies Cell biology, focusing on Rap1 in particular. Her T cell research is multidisciplinary, incorporating perspectives in Cytotoxic T cell, Anaerobic glycolysis and Effector.
Her Cancer research study integrates concerns from other disciplines, such as Cancer immunotherapy, Immunotherapy and Myelopoiesis. The study incorporates disciplines such as Receptor, Signal transduction, Antigen and Lymphocyte in addition to Immune system. Vassiliki A. Boussiotis has included themes like After treatment and Hematopoietic stem cell transplantation, Transplantation in her Immunology study.
Her primary areas of investigation include T cell, Cell biology, Immune system, Immunotherapy and Cancer immunotherapy. Her work deals with themes such as Tyrosine, Anaerobic glycolysis, Phosphorylation, Lipid metabolism and Effector, which intersect with T cell. Her Cell biology study which covers Acquired immune system that intersects with IL-2 receptor, Antigen-presenting cell, Central tolerance, ZAP70 and Cytotoxic T cell.
Vassiliki A. Boussiotis interconnects Cell, Receptor, Signal transduction, Vaccination and Leukemia in the investigation of issues within Immune system. Her Signal transduction research is multidisciplinary, relying on both Neoplasms therapy, Cell cycle checkpoint, Computational biology and T-cell receptor. Her Cancer immunotherapy study incorporates themes from Peripheral tolerance, Neuroscience, Function and Molecular targets.
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.
PD-L2 is a second ligand for PD-1 and inhibits T cell activation
Yvette Latchman;Clive R. Wood;Tatyana Chernova;Divya Chaudhary.
Nature Immunology (2001)
Cloning of B7-2: A CTLA-4 counter-receptor that costimulates human T cell proliferation
Gordon J. Freeman;John G. Gribben;Vassiliki A. Boussiotis;Judy W. Ng.
Science (1993)
B7-1 and B7-2 do not deliver identical costimulatory signals, since B7-2 but not B7-1 preferentially costimulates the initial production of IL-4
Gordon J. Freeman;Vassiliki A. Boussiotis;Anukanth Anumanthan;Gregory M. Bernstein.
Immunity (1995)
Molecular and Biochemical Aspects of the PD-1 Checkpoint Pathway
Vassiliki A. Boussiotis.
The New England Journal of Medicine (2016)
PD-1 alters T-cell metabolic reprogramming by inhibiting glycolysis and promoting lipolysis and fatty acid oxidation.
Nikolaos Patsoukis;Kankana Bardhan;Pranam Chatterjee;Duygu Sari.
Nature Communications (2015)
CTLA-4 regulates induction of anergy in vivo.
Rebecca J. Greenwald;Vassiliki A. Boussiotis;Robert B. Lorsbach;Abul K. Abbas.
Immunity (2001)
Mouse Inducible Costimulatory Molecule (ICOS) Expression Is Enhanced by CD28 Costimulation and Regulates Differentiation of CD4+ T Cells
Alexander J. McAdam;Alexander J. McAdam;Tammy T. Chang;Anna E. Lumelsky;Edward A. Greenfield.
Journal of Immunology (2000)
Transplantation of anergic histoincompatible bone marrow allografts.
Eva C. Guinan;Vassiliki A. Boussiotis;Donna Neuberg;Lisa LaVita Brennan.
The New England Journal of Medicine (1999)
IL-10–producing T cells suppress immune responses in anergic tuberculosis patients
Vassiliki A. Boussiotis;Eunice Y. Tsai;Edmond J. Yunis;Sok Thim.
Journal of Clinical Investigation (2000)
Maintenance of Human T Cell Anergy: Blocking of IL-2 Gene Transcription by Activated Rap1
Vassiliki A. Boussiotis;Gordon J. Freeman;Alla Berezovskaya;Dwayne L. Barber.
Science (1997)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Harvard University
Harvard University
Harvard University
Harvard University
Harvard University
Harvard University
Queen Mary University of London
Harvard University
Harvard University
Harvard University
Boston University
Polytechnic University of Milan
University of Glasgow
McGill University
National Cheng Kung University
INRAE : Institut national de recherche pour l'agriculture, l'alimentation et l'environnement
University of California, Berkeley
University of Sheffield
Max Planck Society
Dana-Farber Cancer Institute
International Livestock Research Institute
Centro de Investigaciones Energéticas, Medioambientales y Tecnológicas
University of Massachusetts Amherst
Westmead Hospital
Research Triangle Park Foundation
Michigan State University