T cell recognition of fibrinogen. A determinant on the A alpha-chain does not require processing.
about
A step-by-step overview of the dynamic process of epitope selection by major histocompatibility complex class II for presentation to helper T cellsExogenous antigens bind MHC class II first, and are processed by cathepsins laterRubella virus-specific cytotoxic T-lymphocyte responses: identification of the capsid as a target of major histocompatibility complex class I-restricted lysis and definition of two epitopes.Rous-Whipple Award Lecture. Chemical features of peptide selection by the class II histocompatibility molecules.Phagocytosis and protein processing are required for presentation of Cryptococcus neoformans mitogen to T lymphocytesThe MHC class II cofactor HLA-DM interacts with Ig in B cells.T cells specific for alpha-beta interface regions of hemoglobin recognize the isolated subunit but not the tetramer and indicate presentation without processing.Divergent paths for the selection of immunodominant epitopes from distinct antigenic sources.Diversity in MHC class II antigen presentation.Intracellular processing of liposome-encapsulated antigens by macrophages depends upon the antigen.Structural basis of antigen recognition by T lymphocytes. Implications for vaccines.Folding of an MHC class II-restricted tumor antigen controls its antigenicity via MHC-guided processing.Antigen-specific inhibition of CD4(+) T-cell responses to β-lactoglobulin by its single amino acid-substituted mutant form through T-cell receptor antagonism.Class II major histocompatibility complex-restricted T cells specific for a virion structural protein that do not recognize exogenous influenza virus. Evidence that presentation of labile T cell determinants is favored by endogenous antigen synthesiReconstruction of the immunogenic peptide RNase(43-56) by identification and transfer of the critical residues into an unrelated peptide backbone.Determinant capture as a possible mechanism of protection afforded by major histocompatibility complex class II molecules in autoimmune diseaseDirect binding of a synthetic multichain polypeptide to class II major histocompatibility complex molecules on antigen-presenting cells and stimulation of a specific T-cell line require processing of the polypeptide.Cellular mechanisms of antigen processing and the function of class I and II major histocompatibility complex molecules.The endosome-lysosome pathway and information generation in the immune system.Toward a Network Model of MHC Class II-Restricted Antigen Processing.Determinants of immunodominance for CD4 T cells.Reconstruction of a pathway of antigen processing and class II MHC peptide capture.Distinct antigen MHC class II complexes generated by separate processing pathways.Conformation-dependent recognition of a protein by T cells requires presentation without processing.T cell responses affected by aminopeptidase N (CD13)-mediated trimming of major histocompatibility complex class II-bound peptides.The effect of lipoylation on CD4 T-cell recognition of the 19,000 MW Mycobacterium tuberculosis antigen
P2860
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P2860
T cell recognition of fibrinogen. A determinant on the A alpha-chain does not require processing.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
T cell recognition of fibrinog ...... n does not require processing.
@en
type
label
T cell recognition of fibrinog ...... n does not require processing.
@en
prefLabel
T cell recognition of fibrinog ...... n does not require processing.
@en
P2093
P1476
T cell recognition of fibrinog ...... in does not require processing
@en
P2093
P304
P407
P577
1988-02-01T00:00:00Z