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suck abstract from ncbi

pmid2472452      J+Immunol 1989 ; 143 (2): 762-9
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  • Human T cell clones present antigen #MMPMID2472452
  • Hewitt CR; Feldmann M
  • J Immunol 1989[Jul]; 143 (2): 762-9 PMID2472452show ga
  • Two human T cells clones are described which react with influenza virus hemagglutinin type H3 and synthetic peptides of H3 when presented by PBMC APC. Both T cell clones also responded to peptide Ag in the absence of additional APC suggesting that T cells can simultaneously present and respond to Ag. T cell clones could only present peptide Ag and not an appropriate strain of inactivated whole influenza virus thus indicating an inability to process Ag conventionally. Peptide presentation by T cells was dose dependent, restricted by MHC class II Ag and was dependent on the number of Ag presenting T cells per culture. Experiments with nested peptides showed that the same epitope was recognized in the presence and absence of PBMC APC. No Ag or IL-2 from the propagation procedure was carried over into assays and two-color fluorescence-activated cell sorter analysis of each clone detected no contaminating cells with the phenotype of monocytes, macrophages or B cells; in each T cell clone, all cells expressing MHC class II Ag co-expressed CD3. These date therefore provide strong evidence that human T cell clones can simultaneously present and respond to appropriate forms of Ag.
  • |Amino Acid Sequence[MESH]
  • |Antigen-Presenting Cells/classification/*immunology[MESH]
  • |Antigens, Viral/*immunology[MESH]
  • |Clone Cells/immunology[MESH]
  • |Epitopes/immunology[MESH]
  • |HLA-D Antigens/immunology[MESH]
  • |Humans[MESH]
  • |Influenza A virus/*immunology[MESH]
  • |Kinetics[MESH]
  • |Leukocytes, Mononuclear/immunology[MESH]
  • |Molecular Sequence Data[MESH]


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