Literature DB >> 2531954

C-terminal domain of the adenovirus E1A oncogene product is required for induction of cytotoxic T lymphocytes and tumor-specific transplantation immunity.

D Urbanelli1, Y Sawada, J Raskova, N C Jones, T Shenk, K Raska.   

Abstract

Adenovirus genes required for the elicitation of adenovirus group C-specific cytolytic T lymphocytes (CTLs) and for the induction of adenovirus-specific transplantation antigen (TSTA) were identified by immunization with a library of adenovirus mutants. The group C Ad-specific CTL response was elicited by immunization with wild-type adenovirus type 5 (Ad5) or with recombinant adenoviruses containing Ad5 E1A gene. The specific CTL response was also elicited by Ad5 virus constructs which express only the 12 S or 13 S E1A early mRNA, but not with viruses unable to express E1A protein sequences normally encoded by the E1A early messages. The induction of transplantation immunity against tumorigenic Ad-transformed cells was studied next. The product encoded by either 13 S and 12 S E1A mRNA alone was sufficient for strong TSTA activity. A series of viruses with mutations within the first exon of the E1A message also induced strong TSTA, while Ad5 mutants with lesions within the second exon failed to induce syngraft immunity. These results provide strong evidence that amino acid sequence encoded by the second exon of the Ad5 E1A message is required, either directly or indirectly, for the induction of both Ad-specific CTL and Ad TSTA.

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Year:  1989        PMID: 2531954     DOI: 10.1016/0042-6822(89)90572-2

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  8 in total

1.  The reovirus nonstructural protein sigma1NS is recognized by murine cytotoxic T lymphocytes.

Authors:  L M Hoffman; K T Hogan; L W Cashdollar
Journal:  J Virol       Date:  1996-11       Impact factor: 5.103

2.  Molecular cloning and characterization of a cellular phosphoprotein that interacts with a conserved C-terminal domain of adenovirus E1A involved in negative modulation of oncogenic transformation.

Authors:  U Schaeper; J M Boyd; S Verma; E Uhlmann; T Subramanian; G Chinnadurai
Journal:  Proc Natl Acad Sci U S A       Date:  1995-11-07       Impact factor: 11.205

3.  The role of mouse adenovirus type 1 early region 1A in acute and persistent infections in mice.

Authors:  K Smith; C C Brown; K R Spindler
Journal:  J Virol       Date:  1998-07       Impact factor: 5.103

4.  Induction of gene expression by exon 2 of the major E1A proteins of adenovirus type 5.

Authors:  J S Mymryk; S T Bayley
Journal:  J Virol       Date:  1993-12       Impact factor: 5.103

5.  Adenovirus E1A proteins stimulate inositol phospholipid metabolism in PC12 cells.

Authors:  K Shiroki; A Yamakawa; M Shibata; T Takenawa; S Sugano; A Nomoto
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

6.  Constructing chimeric type 12/type 5 adenovirus E1A genes and using them to identify an oncogenic determinant of adenovirus type 12.

Authors:  G C Telling; J Williams
Journal:  J Virol       Date:  1994-02       Impact factor: 5.103

7.  Highly efficient focus formation by Rous sarcoma virus on adenovirus type 12 E1A-transformed rat 3Y1 cells.

Authors:  K Shiroki; M Hamaguchi; S Kawai
Journal:  J Virol       Date:  1992-03       Impact factor: 5.103

8.  A region in the C-terminus of adenovirus 2/5 E1a protein is required for association with a cellular phosphoprotein and important for the negative modulation of T24-ras mediated transformation, tumorigenesis and metastasis.

Authors:  J M Boyd; T Subramanian; U Schaeper; M La Regina; S Bayley; G Chinnadurai
Journal:  EMBO J       Date:  1993-02       Impact factor: 11.598

  8 in total

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