Melanoma cells and normal melanocytes share antigens recognized by HLA-A2-restricted cytotoxic T cell clones from melanoma patients - PubMed (original) (raw)
Melanoma cells and normal melanocytes share antigens recognized by HLA-A2-restricted cytotoxic T cell clones from melanoma patients
A Anichini et al. J Exp Med. 1993.
Abstract
HLA-A2-restricted, CD3+, CD8+, alpha/beta+ cytotoxic T cell (CTL) clones were isolated from peripheral blood (PBL) or tumor infiltrating lymphocytes (TIL) of two HLA-A2+ melanoma patients (9742 and 5810), to evaluate the possible recognition of autologous melanoma and of allogeneic HLA-A2-matched normal melanocytes. These CTL clones lysed not only fresh and cultured autologous melanoma cells, but also allogeneic HLA-A2+, but not HLA-A2-, normal melanocytes. The lysis of autologous neoplastic cells and of melanocytes could be inhibited by an anti-HLA-A2 monoclonal antibody (mAb). Lysis of the normal melanocytes was not dependent on the presence of human or fetal calf serum in the culture medium. HLA-A2-restricted CTL clones recognized not only proliferating melanocytes cultured in complete melanocyte medium, but also melanocytes made quiescent by culture for up to 6 d in a basal medium devoid of exogenous factors such as phorbol ester (O-tetradecanoyl phorbol 13-acetate [TPA]), epidermal growth factor, insulin, and pituitary extracts. Analysis of specificity of four CTL clones (A75, A83, A94, and 119) from patient 9742, performed on a panel of 39 targets, indicated that the three HLA-A2-restricted CTL (A75, A83, and A94) lysed all but one of nine allogeneic melanomas expressing the HLA-A2 molecule with no reactivity on nine HLA-A2- allogeneic melanomas. Only a few instances of borderline reactivity were seen by the same effectors on 21 targets of nonmelanocyte lineage, including 12 carcinomas of different histology, four Epstein-Barr virus-transformed B cells (lymphoblastoid cell lines [LCL]), including the autologous LCL, four lines of normal fibroblasts, and normal kidney cells. Lack of reactivity on allogeneic targets of nonmelanocyte lineage occurred in spite of expression of HLA-A2 on 14 of these targets as determined by conventional tissue typing and cytofluorimetric analysis with four different anti-HLA-A2 mAb. These data indicate that tissue-related antigens can be expressed on normal and neoplastic cells of the melanocyte lineage and can be recognized in association with HLA-A2 by CTL clones from melanoma patients.
Similar articles
- T cell receptor (TCR) structure of autologous melanoma-reactive cytotoxic T lymphocyte (CTL) clones: tumor-infiltrating lymphocytes overexpress in vivo the TCR beta chain sequence used by an HLA-A2-restricted and melanocyte-lineage-specific CTL clone.
Sensi M, Salvi S, Castelli C, Maccalli C, Mazzocchi A, Mortarini R, Nicolini G, Herlyn M, Parmiani G, Anichini A. Sensi M, et al. J Exp Med. 1993 Oct 1;178(4):1231-46. doi: 10.1084/jem.178.4.1231. J Exp Med. 1993. PMID: 8376931 Free PMC article. - Cytotoxic T cells directed to tumor antigens not expressed on normal melanocytes dominate HLA-A2.1-restricted immune repertoire to melanoma.
Anichini A, Mortarini R, Maccalli C, Squarcina P, Fleischhauer K, Mascheroni L, Parmiani G. Anichini A, et al. J Immunol. 1996 Jan 1;156(1):208-17. J Immunol. 1996. PMID: 8598464 - Recognition of shared melanoma antigen by HLA-A2-restricted cytolytic T cell clones derived from human tumor-infiltrating lymphocytes.
Viret C, Davodeau F, Guilloux Y, Bignon JD, Semana G, Breathnach R, Jotereau F. Viret C, et al. Eur J Immunol. 1993 Jan;23(1):141-6. doi: 10.1002/eji.1830230123. Eur J Immunol. 1993. PMID: 8419164 - New tumour-restricted melanoma antigens as defined by cytotoxic T-cell responses.
Parmiani G, Anichini A, Castelli C. Parmiani G, et al. Melanoma Res. 1997 Aug;7 Suppl 2:S95-8. Melanoma Res. 1997. PMID: 9578423 Review. - Antitumor cytotoxic T-lymphocyte response in human lung carcinoma: identification of a tumor-associated antigen.
Mami-Chouaib F, Echchakir H, Dorothée G, Vergnon I, Chouaib S. Mami-Chouaib F, et al. Immunol Rev. 2002 Oct;188:114-21. doi: 10.1034/j.1600-065x.2002.18810.x. Immunol Rev. 2002. PMID: 12445285 Review.
Cited by
- A new gene coding for a differentiation antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas.
Coulie PG, Brichard V, Van Pel A, Wölfel T, Schneider J, Traversari C, Mattei S, De Plaen E, Lurquin C, Szikora JP, Renauld JC, Boon T. Coulie PG, et al. J Exp Med. 1994 Jul 1;180(1):35-42. doi: 10.1084/jem.180.1.35. J Exp Med. 1994. PMID: 8006593 Free PMC article. - Human tumor antigens recognized by T-cells.
Kawakami Y, Rosenberg SA. Kawakami Y, et al. Immunol Res. 1997;16(4):313-39. doi: 10.1007/BF02786397. Immunol Res. 1997. PMID: 9439758 Review. - Cancer gene and immunotherapy: recent developments.
Jantscheff P, Herrmann R, Rochlitz C. Jantscheff P, et al. Med Oncol. 1999 Jul;16(2):78-85. doi: 10.1007/BF02785840. Med Oncol. 1999. PMID: 10456655 Review. - Generation of specific anti-melanoma reactivity by stimulation of human tumor-infiltrating lymphocytes with MAGE-1 synthetic peptide.
Salgaller ML, Weber JS, Koenig S, Yannelli JR, Rosenberg SA. Salgaller ML, et al. Cancer Immunol Immunother. 1994 Aug;39(2):105-16. doi: 10.1007/BF01525316. Cancer Immunol Immunother. 1994. PMID: 7519125 Free PMC article. - Tumor escape from immune recognition: lethal recurrent melanoma in a patient associated with downregulation of the peptide transporter protein TAP-1 and loss of expression of the immunodominant MART-1/Melan-A antigen.
Maeurer MJ, Gollin SM, Martin D, Swaney W, Bryant J, Castelli C, Robbins P, Parmiani G, Storkus WJ, Lotze MT. Maeurer MJ, et al. J Clin Invest. 1996 Oct 1;98(7):1633-41. doi: 10.1172/JCI118958. J Clin Invest. 1996. PMID: 8833913 Free PMC article.
References
- Proc Natl Acad Sci U S A. 1983 Mar;80(5):1337-41 - PubMed
- Immunogenetics. 1983;18(1):23-35 - PubMed
- J Invest Dermatol. 1985 Aug;85(2):169-74 - PubMed
- Eur J Immunol. 1987 Jan;17(1):105-11 - PubMed
- J Exp Med. 1987 Mar 1;165(3):812-29 - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials