Approval Year
Substance Class |
Protein
Created
by
admin
on
Edited
Sat Dec 16 15:38:59 GMT 2023
by
admin
on
Sat Dec 16 15:38:59 GMT 2023
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Protein Type | PEPTIDE |
Protein Sub Type | |
Record UNII |
OGZ705E0UN
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Record Status |
Validated (UNII)
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Record Version |
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-
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Name | Type | Language | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
Classification Tree | Code System | Code | ||
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EU-Orphan Drug |
EU/3/16/1634
Created by
admin on Sat Dec 16 15:38:59 GMT 2023 , Edited by admin on Sat Dec 16 15:38:59 GMT 2023
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Code System | Code | Type | Description | ||
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146014907
Created by
admin on Sat Dec 16 15:38:59 GMT 2023 , Edited by admin on Sat Dec 16 15:38:59 GMT 2023
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PRIMARY | |||
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344422-47-5
Created by
admin on Sat Dec 16 15:38:59 GMT 2023 , Edited by admin on Sat Dec 16 15:38:59 GMT 2023
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PRIMARY | |||
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OGZ705E0UN
Created by
admin on Sat Dec 16 15:38:59 GMT 2023 , Edited by admin on Sat Dec 16 15:38:59 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |
The existence of overlapping CD8 and CD4 T-cell epitopes within certain tumor antigens provides an opportunity to test the hypothesis that
relatively short peptides could be used to generate both CD8 and CD4 T cells against tumor. In this report, T-cell responses to a fragment of the tumor antigen NY-ESO-1 that contained an HLA-DP4-restricted helper T
cell epitope as well as an HLA-A2-restricted cytotoxic T cell epitope were analyzed. One peptide, ESO:157170 (SLLMWITQCFLPVF) was recognized by both NY-ESO-1-reactive CD8 and CD4 T-cell clones. Both CD4 and CD8 T cells were efficiently generated from the peripheral
blood of multiple melanoma patients after in vitro stimulations using
ESO:157170. Dual-specific peptides containing both cytotoxic T-cell and
helper T-cell epitopes may represent an attractive strategy of vaccine
design aimed at generating tumor-reactive CD4 and CD8 T cells.
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ACTIVE MOIETY |
The most frequently detected response was toward the HLA-DP4-restricted NY-ESO-1(157-170) epitope, which is also recognized by effector T cells. Notably, functional Treg specific for an HLA-DR-restricted epitope within the NY-ESO-1(115-132) peptide were also identified at high frequency in tumor tissue, suggesting that NY-ESO-1-specific Treg may suppress local anti-tumor immune responses. Together, our data provide compelling evidence for the ability of a cancer vaccine to expand tumor antigen-specific Treg in the setting of advanced cancer, a finding which should be given serious consideration in the design of future cancer vaccine clinical trials.
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Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Molecular Formula | CHEMICAL |
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MOL_WEIGHT:NUMBER(CALCULATED) | CHEMICAL |
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