Transfers Reduced Reactivity with Irrelevant Peptide-Independent Alloreactive TCR Chain That Forms β TCR
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Courtney Smith | John T. Harty | Stanislav Vukmanovic | Fabio R. Santori | Zoran Popmihajlov | J. Harty | Courtney M. Smith | Z. Popmihajlov | F. R. Santori | S. Vukmanović
[1] W. Lie,et al. Disparate interaction of peptide ligand with nascent versus mature class I major histocompatibility complex molecules: comparisons of peptide binding to alternative forms of Ld in cell lysates and the cell surface , 1992, The Journal of experimental medicine.
[2] M. Bevan,et al. Hypothesis: why do so many lymphocytes respond to major histocompatibility antigens? , 1977, Cellular immunology.
[3] T. Utsugi,et al. Acceleration of spontaneous diabetes in TCR-beta-transgenic nonobese diabetic mice by beta-cell cytotoxic CD8+ T cells expressing identical endogenous TCR-alpha chains. , 1996, Journal of immunology.
[4] M. Bevan,et al. In thymic selection, peptide diversity gives and takes away. , 1997, Immunity.
[5] S. L. Silins,et al. The influence of antiviral T-cell responses on the alloreactive repertoire. , 1999, Immunology today.
[6] M. Bevan,et al. Characterization of dual-reactive H-2Kb-restricted anti-vesicular stomatitus virus and alloreactive cytotoxic T cells. , 1987, Journal of immunology.
[7] M. Gross,et al. I-Ep-Bound Self-Peptides: Identification, Characterization, and Role in Alloreactivity1 , 2006, The Journal of Immunology.
[8] J. Harty,et al. Duration of Infection and Antigen Display Have Minimal Influence on the Kinetics of the CD4+ T Cell Response to Listeria monocytogenes Infection1 , 2004, The Journal of Immunology.
[9] L. Sherman,et al. Peptide-dependent recognition of H–2Kb by alloreactive cytotoxic T lymphocytes , 1989, Nature.
[10] Bernard Malissen,et al. What do TCR-pMHC crystal structures teach us about MHC restriction and alloreactivity? , 2003, Trends in immunology.
[11] D. Ostrov,et al. Highly Homologous Ligands Distinct Footprints of TCR Engagement with , 2004 .
[12] J. Harty,et al. Intracellular staining for TNF and IFN-gamma detects different frequencies of antigen-specific CD8(+) T cells. , 2000, Journal of immunological methods.
[13] M. Sadofsky,et al. The RAG proteins in V(D)J recombination: more than just a nuclease. , 2001, Nucleic acids research.
[14] Robyn L Stanfield,et al. How TCRs bind MHCs, peptides, and coreceptors. , 2006, Annual review of immunology.
[15] H. Pircher,et al. Tolerance induction in double specific T-cell receptor transgenic mice varies with antigen , 1989, Nature.
[16] M. Marić,et al. Factors influencing the patterns of T lymphocyte allorecognition. , 2002, Transplantation.
[17] K. Garcia,et al. Not just any T cell receptor will do. , 2003, Immunity.
[18] J. Smith,et al. Model for the in vivo assembly of nascent Ld class I molecules and for the expression of unfolded Ld molecules at the cell surface , 1993, The Journal of experimental medicine.
[19] M. Bevan,et al. High determinant density may explain the phenomenon of alloreactivity. , 1984, Immunology today.
[20] P. Kourilsky,et al. Impact of negative selection on the T cell repertoire reactive to a self-peptide: a large fraction of T cell clones escapes clonal deletion. , 2000, Immunity.
[21] H. Eisen,et al. A naturally occurring peptide recognized by alloreactive CD8+ cytotoxic T lymphocytes in association with a class I MHC protein , 1992, Cell.
[22] K. Jhaver,et al. The role of protein kinase C in CD8+ T lymphocyte effector responses. , 1997, Journal of immunology.
[23] M. Jackson,et al. Peptide-independent Recognition by Alloreactive Cytotoxic T Lymphocytes (CTL) , 1997, The Journal of experimental medicine.
[24] M. Oettinger,et al. V(D)J recombination: site-specific cleavage and repair. , 2000, Molecules and cells.
[25] M. Bevan,et al. Dissection of major histocompatibility complex (MHC) and T cell receptor contact residues in a Kb‐restricted ovalbumin peptide and an assessment of the predictive power of MHC‐binding motifs , 1992, European journal of immunology.
[26] L. Barber,et al. The structural basis of T-cell allorecognition. , 2004, Tissue antigens.
[27] D. Wiley,et al. T Cell Receptor–MHC Interactions up Close , 2001, Cell.
[28] P. Allen,et al. A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR. , 1998, Immunity.
[29] C. Janeway,et al. A molecular map of T cell development. , 1998, Immunity.
[30] D. Ostrov,et al. Distinct Footprints of TCR Engagement with Highly Homologous Ligands1 , 2004, The Journal of Immunology.
[31] M. Bevan,et al. Specific immunity to Listeria monocytogenes in the absence of IFN gamma. , 1995, Immunity.
[32] J. Altman,et al. Negative selection of T cells occurs throughout thymic development. , 1999, Journal of immunology.
[33] P. Fink,et al. V beta 5+ T cell receptors skew toward OVA+H-2Kb recognition. , 1994, Journal of immunology.
[34] H. Rammensee,et al. On the nature of peptides involved in T cell alloreactivity , 1991, The Journal of experimental medicine.
[35] J. Yewdell,et al. Effect of TAP on the generation and intracellular trafficking of peptide-receptive major histocompatibility complex class I molecules. , 1995, Immunity.
[36] M. Bevan. Killer cells reactive to altered-self antigens can also be alloreactive. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[37] Y. Chien,et al. Induction of rapid T cell activation and tolerance by systemic presentation of an orally administered antigen. , 1998, Immunity.
[38] T. Elliott,et al. Cytotoxic T lymphocytes recognize a reconstituted class I histocompatibility antigen (HLA-A2) as an allogeneic target molecule. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[39] R. Schwartz,et al. High frequency and nonrandom distribution of alloreactivity in T cell clones selected for recognition of foreign antigen in association with self class II molecules. , 1986, Journal of immunology.