Literature DB >> 1281166

Novel LCMV-specific H-2k restricted CTL clones recognize internal viral gene products and cause CNS disease.

H Lewicki1, T A McKee, A Tishon, M Salvato, J L Whitton, M B Oldstone.   

Abstract

H-2k (C3H/Hej) cytotoxic T lymphocytes (CTL) specific for lymphocytic choriomeningitis virus (LCMV) were cloned. Three clones recognizing internal viral antigens were studied. One such CTL clone recognized neither the glycoprotein nor nucleoprotein encoded by the viral short RNA segment, but reacted with a protein encoded by the long RNA segment, either the viral polymerase, or the Z protein. This one clone, in addition to primary CTL harvested from immunized C3H mice, failed to lyse target cells expressing the Z protein, suggesting recognition was to the viral polymerase. Two other clones recognized the viral nucleoprotein, amino acids 93-100, as determined by protein deletion and peptide mapping studies. When introduced directly into the central nervous systems of LCMV-infected histocompatible mice, all clones were active in vivo and capable of causing immunopathologically mediated death.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1281166     DOI: 10.1016/0165-5728(92)90190-v

Source DB:  PubMed          Journal:  J Neuroimmunol        ISSN: 0165-5728            Impact factor:   3.478


  5 in total

Review 1.  Coverage of related pathogenic species by multivalent and cross-protective vaccine design: arenaviruses as a model system.

Authors:  Jason Botten; John Sidney; Bianca R Mothé; Bjoern Peters; Alessandro Sette; Maya F Kotturi
Journal:  Microbiol Mol Biol Rev       Date:  2010-06       Impact factor: 11.056

2.  Murine infection with lymphocytic choriomeningitis virus following gastric inoculation.

Authors:  S K Rai; D S Cheung; M S Wu; T F Warner; M S Salvato
Journal:  J Virol       Date:  1996-10       Impact factor: 5.103

3.  Discriminated selection among viral peptides with the appropriate anchor residues: implications for the size of the cytotoxic T-lymphocyte repertoire and control of viral infection.

Authors:  M B Oldstone; H Lewicki; P Borrow; D Hudrisier; J E Gairin
Journal:  J Virol       Date:  1995-12       Impact factor: 5.103

4.  Focal expression of interleukin-2 does not break unresponsiveness to "self" (viral) antigen expressed in beta cells but enhances development of autoimmune disease (diabetes) after initiation of an anti-self immune response.

Authors:  M G von Herrath; J Allison; J F Miller; M B Oldstone
Journal:  J Clin Invest       Date:  1995-02       Impact factor: 14.808

5.  Interferon-gamma is essential for destruction of beta cells and development of insulin-dependent diabetes mellitus.

Authors:  M G von Herrath; M B Oldstone
Journal:  J Exp Med       Date:  1997-02-03       Impact factor: 14.307

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.