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Showing 1 to 8 of 8 for “"peptide-MHC complexes"”.

  1. In silico prediction of C57BL/6 mouse T-cell epitopes: enhancing immunogenicity assessment with PREDBL6

    The MHC class I antigen processing pathway involves multiple steps: 1) the proteasome selectively cleaves intracellular proteins into short peptides, typically 8–11 amino acids long; 2) TAPs (transporter associated with antigen processing) selectively transport some of these peptides to the …

    bu Repository record for In silico prediction of C57BL/6 mouse T-cell epitopes: enhancing immunogenicity assessment with PREDBL6 (opens in a new tab)

  2. Expanding Antigen-specific Tr1 Cells to Treat Autoimmunity

    … therapy which consists of disease-relevant peptide-MHC complexes coated on iron-oxide nanoparticles (NPs). We have demonstrated that the therapeutic effects exerted by these NPs are associated with expansion of antigen-specific T-regulatory-type-1 (Tr1) cells and immuno-suppression of …

    calgary Repository record for Expanding Antigen-specific Tr1 Cells to Treat Autoimmunity (opens in a new tab)

  3. Engineering Proteins Encoded by the Major Histocompatability Complex

    … encoded by the major histocompatability complex (MHC) were initially discovered based on their role in skin graft rejections. Years later, the physiological function of MHC proteins, as key players in the immune response to foreign pathogens, was elucidated. For instance, class I major …

    uiuc Repository record for Engineering Proteins Encoded by the Major Histocompatability Complex (opens in a new tab)

  4. Elucidating the functional states of tumor-resident dendritic cells that drive productive anti-tumor immunity

    … by crossdressing with pre-formed tumor-derived peptide-MHC complexes. We determined that constitutive tumor cell-derived type-I-interferon (IFN-I) production in regressor tumors was driving the ISG+ DC state. Ablation of tumor cell-derived IFN-I in regressor tumors led to complete loss of …

    mit Repository record for Elucidating the functional states of tumor-resident dendritic cells that drive productive anti-tumor immunity (opens in a new tab)

  5. Stochastic and spatiotemporal effects in T-cell signaling

    … interaction between T cell receptors (TCR) and peptide-MHC complexes (pMHC), the second on the equilibrium affinity (KD). We study an extensive set of TCR-pMHC interactions in CD4+ T cells which have differential KD and kinetics of binding. The data indicate that ligands with short t1/2 can be …

    mit Repository record for Stochastic and spatiotemporal effects in T-cell signaling (opens in a new tab)

  6. Novel peptide antigens provide insights into the recognition process by T cells

    … the reactivity of T cell receptors with novel peptide antigens. The first study (Chapter 2) described a collection of novel peptide antigens for a single T cell receptor and their diverse requirements for the co-receptor CD8. One of the peptides showed no activity despite binding the TCR, and …

    uiuc Repository record for Novel peptide antigens provide insights into the recognition process by T cells (opens in a new tab)

  7. Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies

    … αβ T cell receptor (TCR). The TCR recognizes a peptide epitope presented by a product of the major histocompatibility complex (MHC). All nucleated cells express class I MHC products, typically in association with one of thousands of “self” peptides. However, during a viral infection, “foreign” …

    uiuc Repository record for Recognition of hepatitis B epitopes by T cell receptors and T cell receptor-like antibodies (opens in a new tab)

  8. THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY

    … IL-2, CD80 and CD40L singnaling, and weaker peptideMHC I (pMHC) signaling, Th-APCs stimulated naïve CD8+ T cells to differentiate into effector CTLs, capable of developing into, central memory CTLs. Th-APC-stimulated CD4+ T cells behaved like Th cells in function, augmenting the overall …

    sask Repository record for THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY (opens in a new tab)