VACCINATION WITH CYTOTOXIC T-LYMPHOCYTE EPITOPE-CONTAINING PEPTIDE PROTECTS AGAINST A TUMOR-INDUCED BY HUMAN PAPILLOMAVIRUS TYPE-16-TRANSFORMED CELLS

被引:733
作者
FELTKAMP, MCW
SMITS, HL
VIERBOOM, MPM
MINNAAR, RP
DEJONGH, BM
DRIJFHOUT, JW
TERSCHEGGET, J
MELIEF, CJM
KAST, WM
机构
[1] UNIV HOSP LEIDEN, DEPT IMMUNOHEMATOL & BLOOD BANK, BLDG 1 E3-Q, POB 9600, 2300 RC LEIDEN, NETHERLANDS
[2] UNIV AMSTERDAM, ACAD MED CTR, DEPT VIROL, FUNDAMENTAL VIROL SECT, 1105 AZ AMSTERDAM, NETHERLANDS
关键词
CYTOTOXIC T-LYMPHOCYTE EPITOPE; PEPTIDE VACCINATION; TUMOR PROTECTION; PEPTIDE-BINDING MOTIF; PAPILLOMAVIRUS;
D O I
10.1002/eji.1830230929
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytotoxic T lymphocyte (CTL) peptide epitopes can be used for immunization of mice against lethal virus infection. To study whether this approach can be successful against virus-induced tumors we generated a B6 (H-2b) tumorigenic cell line transformed by human papillomavirus (HPV). This virus is detected in over 90% of all human cervical cancers. To identify vaccine candidates, we generated a set of 240 overlapping peptides derived from the HPV type 16 (HPV16) oncogenes E6 and E7. These peptides were tested for their ability to bind H-2K(b) and H-2D(b) MHC class I molecules. Binding peptides were compared with the presently known peptide-binding motifs for H-2K(b) and H-2D(b) and the predictive value of these motifs is shortly discussed. The high-affinity H-2D(b)-binding peptide and putative CTL epitope E7 49-57 (RAHYNIVTF) was used in vaccination studies against HPV 16-transformed tumor cells. Immunization with peptide E7 49-57 rendered mice insensitive to a subsequent challenge with HPV 16-transformed tumor cells in vivo, and induced a CTL response which lysed the tumor cells in vitro.
引用
收藏
页码:2242 / 2249
页数:8
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