Abstract |
MART-1 is a good candidate antigen for immunotherapy against HLA-A2 patients with melanoma, since it is a highly immunogenic antigen recognized by HLA-A2 and HLA-B45 restricted CD8+ cytotoxic T cells and expressed in the majority of melanoma lesions. In the present study the expression of MART-1 and HLA-A2 on melanocytic cells and CD8+ T cell infiltration was immunohistochemically analyzed. MART-1 was expressed in most melanocytic lesions, while HLA-A2 was down-regulated with melanoma disease progression. Furthermore, concomitant down-regulation of MART-1 and HLA-A2 in melanoma cells was correlated with poor prognosis. These findings suggest both MART-1 and HLA-A2 expression in melanoma lesions should be analyzed for selection of patients eligible for MART-1 based immunotherapy and monitoring for emergence of melanoma cells resistant to T cell therapy.
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Authors | T Kageshita, Y Kawakami, T Ono |
Journal | Journal of dermatological science
(J Dermatol Sci)
Vol. 25
Issue 1
Pg. 36-44
(Jan 2001)
ISSN: 0923-1811 [Print] Netherlands |
PMID | 11154862
(Publication Type: Journal Article)
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Chemical References |
- Antigens, Neoplasm
- HLA-A2 Antigen
- Histocompatibility Antigens Class I
- MART-1 Antigen
- MLANA protein, human
- Neoplasm Proteins
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Topics |
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Antigens, Neoplasm
- CD8-Positive T-Lymphocytes
(pathology)
- Child
- Female
- HLA-A2 Antigen
(metabolism)
- Histocompatibility Antigens Class I
(metabolism)
- Humans
- Immunohistochemistry
(methods)
- Lymphocytes, Tumor-Infiltrating
(pathology)
- MART-1 Antigen
- Male
- Melanocytes
(pathology)
- Melanoma
(metabolism, pathology)
- Middle Aged
- Neoplasm Proteins
(metabolism)
- Skin Diseases
(metabolism, pathology)
- Skin Neoplasms
(metabolism, pathology)
- Staining and Labeling
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