Literature DB >> 6245128

Resistance to fatal central nervous system disease by mouse hepatitis virus, strain JHM. II. Adherent cell-mediated protection.

S A Stohlman, J A Frelinger, L P Weiner.   

Abstract

Resistance of SJL/J mice to intracranial inoculation with the JHM strain of mouse hepatitis, a coronavirus, is dependent upon the age of the animals at inoculation. Animals 12 weeks of age or older are resistant, whereas those 6 weeks or younger are uniformly susceptible to viral infection. Spleen cells or thioglycolate elicited peritoneal exudate cells can transfer resistance from 12-week-old to 6-week-old recipients. Removal of the adherent cells from either spleen or peritoneal cells ablated protection. Adherent cells from 12-week-old mice were protective even after depletion of Ia- and Thy-1-bearing cells. Antiviral antibody, thioglycolate injection into 6-week-old animals, and nylon wool-purified T cells were ineffective in mediating resistance. Adherent cells transferred 4 days before virus challenge, but not after challenge, were protective. Thus, there is an age-related change in SJL mice that protects from acute central nervous system disease, which may be due to maturation of a specialized adherent cell population.

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Year:  1980        PMID: 6245128

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


  24 in total

1.  SJL/J mice are highly susceptible to infection by mouse adenovirus type 1.

Authors:  K R Spindler; L Fang; M L Moore; G N Hirsch; C C Brown; A Kajon
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

2.  Differential susceptibility and resistance of immunocompetent and immunodeficient mice to fatal Hantaan virus infection.

Authors:  T Nakamura; R Yanagihara; C J Gibbs; H L Amyx; D C Gajdusek
Journal:  Arch Virol       Date:  1985       Impact factor: 2.574

3.  Analysis of age-dependent resistance to murine coronavirus JHM infection in mice.

Authors:  K Pickel; M A Müller; V ter Meulen
Journal:  Infect Immun       Date:  1981-12       Impact factor: 3.441

4.  Macrophage antiviral activity: extrinsic versus intrinsic activity.

Authors:  S A Stohlman; J G Woodward; J A Frelinger
Journal:  Infect Immun       Date:  1982-05       Impact factor: 3.441

5.  Characterization of a variant virus selected in rat brains after infection by coronavirus mouse hepatitis virus JHM.

Authors:  F Taguchi; S G Siddell; H Wege; V ter Meulen
Journal:  J Virol       Date:  1985-05       Impact factor: 5.103

6.  In vivo and in vitro models of demyelinating disease: endogenous factors influencing demyelinating disease caused by mouse hepatitis virus in rats and mice.

Authors:  O Sorensen; R Dugre; D Percy; S Dales
Journal:  Infect Immun       Date:  1982-09       Impact factor: 3.441

7.  Coronavirus species specificity: murine coronavirus binds to a mouse-specific epitope on its carcinoembryonic antigen-related receptor glycoprotein.

Authors:  S R Compton; C B Stephensen; S W Snyder; D G Weismiller; K V Holmes
Journal:  J Virol       Date:  1992-12       Impact factor: 5.103

8.  The receptor for mouse hepatitis virus in the resistant mouse strain SJL is functional: implications for the requirement of a second factor for viral infection.

Authors:  K Yokomori; M M Lai
Journal:  J Virol       Date:  1992-12       Impact factor: 5.103

9.  Selective vulnerability of neural cells and age-related susceptibility to OC43 virus in mice.

Authors:  J Pearson; C A Mims
Journal:  Arch Virol       Date:  1983       Impact factor: 2.574

10.  Several members of the mouse carcinoembryonic antigen-related glycoprotein family are functional receptors for the coronavirus mouse hepatitis virus-A59.

Authors:  G S Dveksler; C W Dieffenbach; C B Cardellichio; K McCuaig; M N Pensiero; G S Jiang; N Beauchemin; K V Holmes
Journal:  J Virol       Date:  1993-01       Impact factor: 5.103

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