His primary areas of study are Immunology, T cell, Lymphocytic choriomeningitis, Cell biology and CD8. Antibody is closely connected to CD40 in his research, which is encompassed under the umbrella topic of Immunology. Within one scientific family, Jason K. Whitmire focuses on topics pertaining to Virology under T cell, and may sometimes address concerns connected to Immunization.
His Lymphocytic choriomeningitis research focuses on Epitope and how it connects with Cell, Virus and Homeostasis. His Cell biology research integrates issues from Naive B cell, Antigen-presenting cell, B-1 cell, Interleukin 21 and CD28. His biological study deals with issues like Natural killer T cell, which deal with fields such as Priming.
Jason K. Whitmire mainly focuses on Immunology, T cell, Virology, Cell biology and CD8. Many of his studies on Immunology involve topics that are commonly interrelated, such as CD40. His research integrates issues of Molecular biology and Histone H3 in his study of T cell.
His study focuses on the intersection of Virology and fields such as Antibody with connections in the field of Picornavirus and Acquired immune system. His work on Effector and Homeostasis is typically connected to Contraction and Chemistry as part of general Cell biology study, connecting several disciplines of science. His CD8 study also includes
Jason K. Whitmire mostly deals with Cell biology, T cell, Pathogenesis, Virus and Effector. The Cell biology study combines topics in areas such as Autoimmunity and CD8. His Pathogenesis study is associated with Immunology.
His work on Spleen, Memory T cell and Viral pathogenesis as part of general Immunology research is often related to Adipocyte and White adipose tissue, thus linking different fields of science. His studies in Virus integrate themes in fields like Picornaviridae, Endocytosis and Endosome, Endolysosome. His Effector course of study focuses on Demethylase activity and Lymphocytic choriomeningitis.
His main research concerns Cell biology, T cell, Effector, Viral replication and General transcription factor. His Cell biology research includes themes of Tumor necrosis factor alpha, Inflammation, Immune system, Experimental autoimmune encephalomyelitis and NLRC3. His T cell study is concerned with the larger field of Immunology.
Jason K. Whitmire has included themes like RNA virus and Interferon regulatory factors in his Effector study.
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Humoral immunity due to long-lived plasma cells
Mark K Slifka;Rustom Antia;Jason K Whitmire;Rafi Ahmed.
Immunity (1998)
Interferon-γ acts directly on CD8+ T cells to increase their abundance during virus infection
Jason K. Whitmire;Joyce T. Tan;J. Lindsay Whitton.
Journal of Experimental Medicine (2005)
4-1BB Ligand, a Member of the TNF Family, Is Important for the Generation of Antiviral CD8 T Cell Responses
Joyce T. Tan;Jason K. Whitmire;Rafi Ahmed;Thomas C. Pearson.
Journal of Immunology (1999)
A Role for Perforin in Downregulating T-Cell Responses during Chronic Viral Infection
Mehrdad Matloubian;M. Suresh;Alison Glass;Marisa Galvan.
Journal of Virology (1999)
Conserved T Cell Receptor Repertoire in Primary and Memory CD8 T Cell Responses to an Acute Viral Infection
David J.D. Sourdive;Kaja Murali-Krishna;John D. Altman;Allan J. Zajac.
Journal of Experimental Medicine (1998)
Role of CD28-B7 interactions in generation and maintenance of CD8 T cell memory
M. Suresh;Jason K. Whitmire;Laurie E. Harrington;Christian P. Larsen.
Journal of Immunology (2001)
Role of CD4 T Cell Help and Costimulation in CD8 T Cell Responses During Listeria monocytogenes Infection
Devon J. Shedlock;Jason K. Whitmire;Joyce Tan;Andrew S. MacDonald.
Journal of Immunology (2003)
Costimulation in antiviral immunity: differential requirements for CD4+ and CD8+ T cell responses
Jason K Whitmire;Rafi Ahmed.
Current Opinion in Immunology (2000)
4-1BB costimulation is required for protective anti-viral immunity after peptide vaccination.
Joyce T. Tan;Jason K. Whitmire;Kaja Murali-Krishna;Rafi Ahmed.
Journal of Immunology (2000)
CD40-CD40 ligand costimulation is required for generating antiviral CD4 T cell responses but is dispensable for CD8 T cell responses.
Jason K. Whitmire;Richard A. Flavell;Iqbal S. Grewal;Iqbal S. Grewal;Christian P. Larsen.
Journal of Immunology (1999)
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