Abstract
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-2Db-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-2b cells, whereas the in vitro primed CTL failed to do so.
MeSH Terms
Animals
Cell Line
Influenza Vaccines/immunology
Lipoproteins/immunology
Mice
Mice, Inbred C57BL
Nucleocapsid Proteins
Nucleoproteins/immunology
Orthomyxoviridae/immunology
RNA-Binding Proteins
T-Lymphocytes, Cytotoxic/immunology
Vaccines, Synthetic/immunology
Viral Core Proteins/immunology
Chemicals
Influenza Vaccines
Lipoproteins
NP protein, Influenza A virus
Nucleocapsid Proteins
Nucleoproteins
RNA-Binding Proteins
Vaccines, Synthetic
Viral Core Proteins
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Schild H
Max-Planck-Institut für Biologie, Abteilung Immungenetik, Tübingen, Germany.
Norda M
Deres K
Falk K
Rötzschke O
Wiesmüller K H
Jung G
Rammensee H G
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