Abstract | BACKGROUND: The authors have demonstrated that immunization with melanoma whole-cell vaccine (MCV) augments T-cell responses to melanoma and that cytotoxic T-cells (CTL) recognize allogeneic melanoma-bearing shared HLA-A antigens. A preclinical model was developed to assess CTL activation in vitro using melanoma lines as stimulators. HLA-A2 expression is predominant in melanoma patients and plays a role in HLA class I restricted CTL killing of melanomas. The authors hypothesized that a MCV consisting of allogeneic HLA-A2 melanomas may be as good as autologous melanoma MCV for HLA-A2 patients. METHODS: CTL were generated from peripheral blood lymphocytes of patients with HLA-A2 melanoma by stimulation with autologous melanoma, allogeneic melanoma (HLA-A2 or non-HLA-A2), or allogeneic MCV (mixed HLA-A2 and non-HLA-A2 melanomas). RESULTS:
HLA-A2 MCV and autologous melanoma were similar and significantly better stimulators than the others. Specificity also was supported by CTL killing and mixed lymphocyte tumor reaction assays. CONCLUSIONS: These studies provide important information for the studying immunization of patients with HLA-A2 melanoma with an allogeneic HLA-A2 MCV in a Phase I clinical trial.
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Authors | Y Hayashi, D S Hoon, L J Foshag, M S Park, P I Terasaki, D L Morton |
Journal | Cancer
(Cancer)
Vol. 72
Issue 3
Pg. 750-9
(Aug 01 1993)
ISSN: 0008-543X [Print] United States |
PMID | 8334627
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antigens, Neoplasm
- HLA-A2 Antigen
- Vaccines
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Topics |
- Antigens, Neoplasm
(immunology)
- Cell Line
- Cytotoxicity, Immunologic
(immunology)
- HLA-A2 Antigen
(immunology)
- Humans
- Immunotherapy
- Lymphocyte Activation
- Melanoma
(immunology, pathology, therapy)
- Phenotype
- T-Lymphocytes, Cytotoxic
(immunology)
- Tumor Cells, Cultured
- Vaccines
(immunology)
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