FINE SPECIFICITY OF CYTOTOXIC LYMPHOCYTES-T PRIMED INVIVO EITHER WITH VIRUS OR SYNTHETIC LIPOPEPTIDE VACCINE OR PRIMED INVITRO WITH PEPTIDE

被引:74
作者
SCHILD, H
NORDA, M
DERES, K
FALK, K
ROTZSCHKE, O
WIESMULLER, KH
JUNG, G
RAMMENSEE, HG
机构
[1] MAX PLANCK INST BIOL,IMMUNGENET ABT,CORRENSTR 42,W-7400 TUBINGEN,GERMANY
[2] UNIV TUBINGEN,INST ORGAN CHEM,W-7400 TUBINGEN 1,GERMANY
关键词
D O I
10.1084/jem.174.6.1665
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Standard synthetic peptide preparations contain numerous peptidic byproducts in small amounts, which may be efficiently recognized by cytotoxic T lymphocytes (CTL). Recognition patterns of such peptide mixtures by CTL may serve as a kind of fingerprint for CTL fine specificity. Three types of H-2D(b)-restricted CTL were compared in this way. CTL primed in vivo either with A/PR/8/34 influenza virus or with a synthetic lipopeptide vaccine prepared from influenza nucleoprotein (NP) peptide 365-380 showed identical fine specificity. Both recognize virus-infected cells. In contrast, CTL primed in vitro with NP 365-380 had a different fine specificity and they did not recognize virus-infected cells. Most significantly, the two in vivo primed CTL types efficiently recognized the natural viral nonapeptide NP 366-374 presented by virus-infected H-2(b) cells, whereas the in vitro primed CTL failed to do so.
引用
收藏
页码:1665 / 1668
页数:4
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