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P. van der Bruggen

Researcher at Ludwig Institute for Cancer Research

Publications -  29
Citations -  7370

P. van der Bruggen is an academic researcher from Ludwig Institute for Cancer Research. The author has contributed to research in topics: Antigen & CTL*. The author has an hindex of 18, co-authored 29 publications receiving 7203 citations.

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Journal ArticleDOI

A gene encoding an antigen recognized by cytolytic T lymphocytes on a human melanoma

TL;DR: In this paper, a gene was identified that directed the expression of antigen MZ2-E on a human melanoma cell line, which belongs to a family of at least three genes.
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Human tumor antigens recognized by t lymphocytes

TL;DR: It appears increasingly unlikely that immunization of patients against one of these antigens will cause harmful immunological side effects caused by the expression of the relevant gene in the testis, and these conclusions are further strengthened by immunization studies carried out with mouse tumor antigen P815A, which is encoded by a gene that is also expressed only in thetestis.
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Human gene MAGE-3 codes for an antigen recognized on a melanoma by autologous cytolytic T lymphocytes.

TL;DR: It is shown here that antigen MZ2-D, which is present on the same tumor, is encoded by another member of the MAGE gene family named MAGE-3, which may have a wide applicability for specific immunotherapy of melanoma patients.
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A nonapeptide encoded by human gene MAGE-1 is recognized on HLA-A1 by cytolytic T lymphocytes directed against tumor antigen MZ2-E.

TL;DR: It is shown that CTL directed against this antigen, which was named MZ2-E, recognize a nonapeptide encoded by the third exon of gene MAGE-1, which opens the possibility of immunizing HLA-A1 patients whose tumor expresses Mage-1 either with the antigenic peptide or with autologous antigen-presenting cells pulsed with the peptide.
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A peptide encoded by human gene MAGE-3 and presented by HLA-A2 induces cytolytic T lymphocytes that recognize tumor cells expressing MAGE-3.

TL;DR: It is reported that the MAGE‐3 gene also codes for another antigenic peptide that is recognized by CTL restricted by HLA‐A2, and the proportion of melanoma tumors expressing this antigen should be approximately 32 % in Caucasian populations.