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Papillomavirus Res ; 2: 21-30, 2016 12.
Article in English | MEDLINE | ID: mdl-27182559

ABSTRACT

Human papillomavirus type 16 (HPV16) infections are intra-epithelial, and thus, HPV16 is known to interact with Langerhans cells (LCs), the resident epithelial antigen-presenting cells (APCs). The current paradigm for APC-mediated induction of T cell anergy is through delivery of T cell receptor signals via peptides on MHC molecules (signal 1), but without costimulation (signal 2). We previously demonstrated that LCs exposed to HPV16 in vitro present HPV antigens to T cells without costimulation, but it remained uncertain if such T cells would remain ignorant, become anergic, or in the case of CD4+ T cells, differentiate into Tregs. Here we demonstrate that Tregs were not induced by LCs presenting only signal 1, and through a series of in vitro immunizations show that CD8+ T cells receiving signal 1 + 2 from LCs weeks after consistently receiving signal 1 are capable of robust effector functions. Importantly, this indicates that T cells are not tolerized but instead remain ignorant to HPV, and are activated given the proper signals.


Subject(s)
Antigen Presentation , Antigens, Viral/immunology , CD4-Positive T-Lymphocytes/immunology , Human papillomavirus 16/immunology , Immune Tolerance , Langerhans Cells/immunology , Antigen-Presenting Cells/immunology , Antigen-Presenting Cells/virology , CD8-Positive T-Lymphocytes/immunology , Cellular Senescence/immunology , Chemokines/immunology , Costimulatory and Inhibitory T-Cell Receptors/immunology , Cytokines/immunology , Humans , Interleukin-2/immunology , Lymphocyte Activation , T-Lymphocytes, Regulatory/immunology
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