Literature DB >> 6313808

Recognition by cytotoxic T lymphocytes of cells expressing fragments of the SV40 tumor antigen.

L R Gooding, K A O'Connell.   

Abstract

Recognition by cytotoxic T lymphocytes (CTL) of syngeneic cells transformed with simian virus 40 (SV40) was examined by using cells expressing known portions of the SV40 early region both as sensitizing cells for stimulation of CTL development and as targets for lysis by CTL. LMTK- cells transfected with a plasmid specifying a 33K amino-terminal fragment of the SV40 tumor (T) antigen served both to stimulate syngeneic CTL capable of lysing SV40 transformed cells and as target cells for CTL generated against syngeneic transformants. The same is true for cells infected with the adenovirus 2-SV40 hybrid viruses, Ad2+ND1 and Ad2+ND2, which produce proteins homologous with carboxy-terminal regions of the SV40 T antigen. These findings indicate that on cells transformed by SV40 virus, and expressing the entire T protein, determinants in both the amino- and carboxy-terminal regions of the molecule are exposed on the cell surface. Furthermore, determinants in both these regions are recognized independently in the polyclonal CTL response to SV40.

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Year:  1983        PMID: 6313808

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  28 in total

1.  The cellular secretory pathway is not utilized for biosynthesis, modification, or intracellular transport of the simian virus 40 large tumor antigen.

Authors:  D L Jarvis; W K Chan; M K Estes; J S Butel
Journal:  J Virol       Date:  1987-12       Impact factor: 5.103

2.  N protein is the predominant antigen recognized by vesicular stomatitis virus-specific cytotoxic T cells.

Authors:  L Puddington; M J Bevan; J K Rose; L Lefrançois
Journal:  J Virol       Date:  1986-11       Impact factor: 5.103

3.  Fine mapping two distinct antigenic sites on simian virus 40 (SV40) T antigen reactive with SV40-specific cytotoxic T-cell clones by using SV40 deletion mutants.

Authors:  R W Anderson; M J Tevethia; D Kalderon; A E Smith; S S Tevethia
Journal:  J Virol       Date:  1988-01       Impact factor: 5.103

4.  Influenza virus-specific cytotoxic T-cell recognition: stimulation of nucleoprotein-specific clones with intact antigen.

Authors:  D C Wraith; A E Vessey
Journal:  Immunology       Date:  1986-10       Impact factor: 7.397

Review 5.  Recognition of influenza virus proteins by cytotoxic T lymphocytes.

Authors:  A R Townsend
Journal:  Immunol Res       Date:  1987       Impact factor: 2.829

Review 6.  Distinguishable pathways of viral antigen presentation to T lymphocytes.

Authors:  L A Morrison; V L Braciale; T J Braciale
Journal:  Immunol Res       Date:  1986       Impact factor: 2.829

7.  Dissection of H-2Db-restricted cytotoxic T-lymphocyte epitopes on simian virus 40 T antigen by the use of synthetic peptides and H-2Dbm mutants.

Authors:  S S Tevethia; M Lewis; Y Tanaka; J Milici; B Knowles; W L Maloy; R Anderson
Journal:  J Virol       Date:  1990-03       Impact factor: 5.103

8.  Immunocytochemical search for JC papovavirus large T-antigen in multiple sclerosis brain tissue.

Authors:  G L Stoner; C F Ryschkewitsch; D L Walker; D Soffer; H D Webster
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

9.  Recognition of typhus group rickettsia-infected targets by human lymphokine-activated killer cells.

Authors:  M Carl; W M Ching; G A Dasch
Journal:  Infect Immun       Date:  1988-09       Impact factor: 3.441

10.  Membrane interactions of simian virus 40 large T-antigen: influence of protein sequences and fatty acid acylation.

Authors:  U Klockmann; M Staufenbiel; W Deppert
Journal:  Mol Cell Biol       Date:  1984-08       Impact factor: 4.272

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