Degradation of the immunogenic peptide gp100280-288 by the monocyte-like U937 cell line

被引:6
作者
Albo, F
Cavazza, A
Giardina, B
Lippa, S
Marini, M
Roda, LG
Spagnoli, G
机构
[1] Univ Roma Tor Vergata, Dipartimento Neurosci, I-00133 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Ist Chim & Chim Clin, I-00168 Rome, Italy
[3] Univ Cattolica Sacro Cuore, Ist Biochim & Biochim Clin, I-00168 Rome, Italy
[4] Univ Basel, Dept Forsch & Chirurg, Basel, Switzerland
关键词
antineoplastic vaccines; tumor-associated antigens; epitopes; enzyme degradation;
D O I
10.1016/S0196-9781(03)00051-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The possible degradation of the tumor antigen epitope gp100(280-288) (YLEPGPVTA) in the presence of the monocyte-like line U937, and the effect of degradation on the in vitro-measured immune recognition, were investigated by chromatographic techniques and immunological assays. Results indicate a rapid hydrolysis of the substrate in the presence of the model cells, which is consistent with the hypothesis that degradation of gp100(280-288) is caused by the activity of U937-expressed enzymes, specifically amino- and carboxypeptidases. On the other hand, these results do not support the involvement of other enzymes known to be expressed by U937 cells. From a functional point of view, these data indicate that the degradation Of gp100(280-288) severely hampered recognition by specific CTL clones. The results obtained may provide a model for epitope degradation by the antigen-presenting cells found in defined anatomical compartments and may, at least in part, account for the low activity of peptide-based antineoplastic vaccines, as well as for the transience of the effects of subcutaneously administered peptides in general. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:371 / 378
页数:8
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