Reference | ||
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Reference Type | Literature | IEDB_Reference:921 |
Title | Epitope focus, clonal composition and Th1 phenotype of the human CD4 response to the secretory mycobacterial antigen Ag85. | |
Authors | M T Valle; A M Megiovanni; A Merlo; G Li Pira; L Bottone; G Angelini; L Bracci; L Lozzi; K Huygen; F Manca | |
Affiliations | Immunology Laboratory, San Martino Hospital and Unit of Retroviral Immunology, Advanced Biotechnology Centre, Genoa, Italy. | |
Journal | Clin Exp Immunol | |
Year | 2001 | |
Abstract | Lymphoproliferation of healthy donors was tested against mycobacterial antigens (PPD, Ag85, Ag85 peptides). All PPD responders recognized the secretory antigen Ag85 and the peptide specificity for Ag85B was defined. Peptide 91-108 was recognized by 85% of donors. In addition, all CD4 T cell lines generated from 12 donors against PPD or Ag85 responded to 91-108. When this peptide was used to generate T cell lines, the cells responded also to tuberculins from atypical mycobacterial species. Thus the cross-reactive peptide behaved as quasi-universal. The analysis of TCR-BV gene usage by cell lines showed that most Ag85-specific T cells correspond to 91-108-specific clonotypes. Intracytoplasmic staining of cell lines after phorbol myristate acetate stimulation resulted in dominance of interferon-gamma (IFN-gamma)-IL-4 double-positive cells, whereas antigen stimulation resulted in production of IFN-gamma only. The data show that peptide 91-108 is the major focus of the CD4 response to mycobacterial antigens in peripheral blood mononuclear cells and in T cell lines from PPD responders. | |
Curation Last Updated | 2023-08-18 20:02:22 |
Epitope | ||
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Epitope ID | 36536 | IEDB_epitope:36536 |
Chemical Type | Linear peptide | |
Linear Sequence | LIGLAMGDAGGYKAADMW | |
Source Molecule Name | alpha-antigen | |
Source Organism | Mycobacterium tuberculosis variant bovis BCG | |
Starting Position | 201 | |
Ending Position | 218 |
Epitope Reference Details | ||
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Epitope Structure Defines | Epitope containing region/antigenic site | |
Epitope Name | Peptide 19 | |
Reference Starting Position | 163 | |
Reference Ending Position | 180 | |
Comments | Source protein and 85A and 85C proteins conform the Ag85 complex. Genbank entry includes the 40aa signal peptide not included in this study, so that different positions are indicated for the epitope. | |
Location of Data in Reference | Author's communication |
Immunization | ||
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Host Organism | Homo sapiens (human) |
1st In Vivo Process | ||
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In Vivo Process Type | Exposure with existing immune reactivity without evidence for disease | |
Disease State | healthy |
Immunization Comments | ||
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Immunization Comments | The donors are PPD+ but otherwise healthy. No information on the origin of the reactivity is provided. |
T Cell Assay | ||
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Qualitative Measurement | Positive | |
Method/Technique | 3H-thymidine | |
Measurement of | proliferation |
Measurement Details | ||
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Number of Subjects Tested | 14 | |
Number of Subjects Responded | 4 | |
Response Frequency (%) | 28.6 |
Effector Cells | ||
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Effector Cell Tissue Type | Blood | |
Effector Cell Type | PBMC | |
Effector Cell Culture Conditions | Direct Ex Vivo |
Antigen Presenting Cells | ||
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Cell Tissue Type | Blood | |
Cell Type | PBMC | |
Cell Culture Conditions | Direct Ex Vivo |
MHC Allele | ||
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MHC Allele Name | HLA class II | |
MHC Evidence Code | T cell assay -Biological process measured |
Antigen | ||
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Epitope Relation | Epitope | |
Chemical Type | Linear peptide | |
Linear Sequence | LIGLAMGDAGGYKAADMW | |
Source Molecule Name | alpha-antigen | |
Source Organism | Mycobacterium tuberculosis variant bovis BCG | |
Starting Position | 201 | |
Ending Position | 218 |
Antigen Details | ||
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Antigen Reference Name | Peptide 19 |
Assay Reference Details | ||
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Assay Comments by IEDB Curator | 28.6% of healthy Purified Protein Derivative positive ( PPD+) individuals studied recognize this peptide with a SI>2. None of the CD4+ T cell lines derived from PMBCs by stimulation with Ag85 or with PPD recognize the peptide. | |
Location of Assay Data in Reference | Figures 1 and 2 |