REJECTION OF A NONIMMUNOGENIC MELANOMA BY VACCINATION WITH NATURAL MELANOMA PEPTIDES ON ENGINEERED ANTIGEN-PRESENTING CELLS

Citation
M. Bellone et al., REJECTION OF A NONIMMUNOGENIC MELANOMA BY VACCINATION WITH NATURAL MELANOMA PEPTIDES ON ENGINEERED ANTIGEN-PRESENTING CELLS, The Journal of immunology, 158(2), 1997, pp. 783-789
Citations number
52
Categorie Soggetti
Immunology
Journal title
The Journal of immunology
ISSN journal
00221767 → ACNP
Volume
158
Issue
2
Year of publication
1997
Pages
783 - 789
Database
ISI
SICI code
0022-1767(1997)158:2<783:ROANMB>2.0.ZU;2-4
Abstract
Naturally processed peptides, obtained by acid extraction of tumor cel ls, contain Ags able to activate specific CTL in vitro. We recently re ported that the nonprofessional APC, RMA-S, expressing the B7.1 molecu le (RMA-S/B7), pulsed with naturally processed peptides from the nonim munogenic B16F1 melanoma (B16F1a.e.) primed syngenic CD8(+) T cells ag ainst the tumor in vitro. Here, we show the rejection of B16F1 melanom a by C57BL/6 mice after immunization with RMA-S/B7 cells pulsed with B 16F1a.e, This response is critically dependent on both CD4(+) and CD8( +) cells, but not on NK cells. However, only CD8(+) T cells exert anti -B16F1 cytolitic activity in vitro. Moreover, RMA-S/B7 cells pulsed wi th B16F1a.e. can be used to prevent the growth of 24-h preestablished melanomas. These results may have important implications for the clini cal use of natural peptide fractions of tumor cells as therapeutic can cer vaccines.