Efficient identification of novel HLA-A(*)0201-presented cytotoxic T lymphocyte epitopes in the widely expressed tumor antigen PRAME by proteasome-mediated digestion analysis. (Q38305306)

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scientific article published on January 2001

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English	Efficient identification of novel HLA-A(*)0201-presented cytotoxic T lymphocyte epitopes in the widely expressed tumor antigen PRAME by proteasome-mediated digestion analysis.	scientific article published on January 2001

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3 November 2019

Efficient identification of novel HLA-A(*)0201-presented cytotoxic T lymphocyte epitopes in the widely expressed tumor antigen PRAME by proteasome-mediated digestion analysis (English)

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3 November 2019

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Pauline Verdijk

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3 November 2019

Peter van Veelen

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J H Kessler

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N J Beekman

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S A Bres-Vloemans

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A M Kloosterman-Joosten

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D C Vissers

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G J ten Bosch

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M G Kester

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J Wouter Drijfhout

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F Ossendorp

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R Offringa

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C J Melief

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1 January 2001

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3 November 2019

Journal of Experimental Medicine

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3 November 2019

1

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73-88

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The cancer germ-line genes MAGE-1, MAGE-3 and PRAME are commonly expressed by human myeloma cells

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Processing of some antigens by the standard proteasome but not by the immunoproteasome results in poor presentation by dendritic cells

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Heterogeneous expression of the tumor-associated antigens RAGE-1, PRAME, and glycoprotein 75 in human renal cell carcinoma: candidates for T-cell-based immunotherapies?

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Two distinct proteolytic processes in the generation of a major histocompatibility complex class I-presented peptide

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The proteolytic fragments generated by vertebrate proteasomes: structural relationships to major histocompatibility complex class I binding peptides

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The protease inhibitor, N-acetyl-L-leucyl-L-leucyl-leucyl-L-norleucinal, decreases the pool of major histocompatibility complex class I-binding peptides and inhibits peptide trimming in the endoplasmic reticulum

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A peptide encoded by the human MAGE3 gene and presented by HLA-B44 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE3.

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The tyrosinase gene codes for an antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas

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Scheme for ranking potential HLA-A2 binding peptides based on independent binding of individual peptide side-chains.

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Cloning of the gene coding for a shared human melanoma antigen recognized by autologous T cells infiltrating into tumor

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Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha

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Proteolytic processing of ovalbumin and beta-galactosidase by the proteasome to a yield antigenic peptides.

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A new gene coding for a differentiation antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas

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Trimming of antigenic peptides in an early secretory compartment

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Definition of a minimal optimal cytotoxic T-cell epitope within the hepatitis B virus nucleocapsid protein.

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Fas ligation induces apoptosis of CD40-activated human B lymphocytes

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hairy cell leukemia-specific recognition by multiple autologous HLA-DQ or DP-restricted T-cell clones

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor regressions observed in patients with metastatic melanoma treated with an antigenic peptide encoded by gene MAGE-3 and presented by HLA-A1

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of proteasome-mediated proteolysis to the hierarchy of epitopes presented by major histocompatibility complex class I molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunogenicity of peptides bound to MHC class I molecules depends on the MHC-peptide complex stability

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An HLA class I peptide-binding assay based on competition for binding to class I molecules on intact human B cells. Identification of conserved HIV-1 polymerase peptides binding to HLA-A*0301

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vaccination of melanoma patients with peptide- or tumor lysate-pulsed dendritic cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/11136822

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1084/JEM.193.1.73

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11136822%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11136822%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11136822%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

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