DIFFERENTIAL EXPRESSION OF CELL-ADHESION MOLECULES CD54 CD11A AND CD58/CD2 BY HUMAN-MELANOMA CELLS AND FUNCTIONAL-ROLE IN THEIR INTERACTIONWITH CYTOTOXIC-CELLS/

Citation
M. Altomonte et al., DIFFERENTIAL EXPRESSION OF CELL-ADHESION MOLECULES CD54 CD11A AND CD58/CD2 BY HUMAN-MELANOMA CELLS AND FUNCTIONAL-ROLE IN THEIR INTERACTIONWITH CYTOTOXIC-CELLS/, Cancer research, 53(14), 1993, pp. 3343-3348
Citations number
34
Categorie Soggetti
Oncology
Journal title
ISSN journal
00085472
Volume
53
Issue
14
Year of publication
1993
Pages
3343 - 3348
Database
ISI
SICI code
0008-5472(1993)53:14<3343:DEOCMC>2.0.ZU;2-G
Abstract
Immunohistochemical staining with monoclonal antibodies showed a diffe rential distribution of intercellular adhesion molecule 1 (ICAM-1/CD54 ) and lymphocyte function-associated antigen 3 (LFA-3/CD58) and their respective counterreceptors lymphocyte function-associated antigens 1 (LFA-1/CD11a) and 2 (LFA-2/CD2) on ten melanoma cell lines and in 46 s urgically removed metastatic melanoma lesions. CD11a and CD2 were not detected on melanoma cells while CD54 and CD58 were coexpressed on the majority of the melanoma cell populations investigated. CD54 showed a higher degree of intra- and intertumor heterogeneity than CD58. Gamma -interferon and/or tumor necrosis factor alpha upregulated the express ion of CD54 by melanoma cells, but neither modulated that of CD58 nor induced that of CD11a and CD2. Anti-CD54 and anti-CD58 monoclonal anti bodies partially inhibited the lysis of melanoma cells by allogeneic n atural killer cells, lymphokine-activated killer cells and, to a great er extent, by autologous tumor-infiltrating lymphocytes. Soluble CD54 (cCD54) purified from serum of patients with melanoma inhibited the ly sis of melanoma cells F0-1 by natural killer cells in a dose-dependent fashion. These results suggest that membrane-bound CD54 and CD58 and cCD54 play a role in host-tumor interactions in patients with malignan t melanoma and may account for the relationship between CD54 expressio n in primary lesions and the clinical course of disease.