Immunocytochemical Detection Of Cytokines In The Lymph Nodes And Brains Of Mice Resistant Or Susceptible To Toxoplasmic Encephalitis

BALB/c mice develop toxoplasmic encephalitis (TE) but the pathology resolves; in contrast, CBA/Ca mice develop progressive TE. Immunohistochemical analysis revealed peak staining for interferon-v (IFN-ã) and tumor necrosis factor (TNF) in lymph nodes of both strains on day 7 of infection, with eleva...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of infectious diseases Vol. 170; no. 4; pp. 939 - 945
Main Authors: Hunter, c. A., Litton, M. J., Remington, J. S., Abrams, J. S.
Format: Journal Article
Language:English
Published: United States The University of Chicago Press 01-10-1994
University of Chicago Press
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:BALB/c mice develop toxoplasmic encephalitis (TE) but the pathology resolves; in contrast, CBA/Ca mice develop progressive TE. Immunohistochemical analysis revealed peak staining for interferon-v (IFN-ã) and tumor necrosis factor (TNF) in lymph nodes of both strains on day 7 of infection, with elevated levels of IFN-ã and TNF persisting in CBA/Ca mice. TNF was present in the central nervous systems (CNS) of both strains of mice and correlated with severity of pathology. Interleukin (IL)-2 was detected in lymph nodes and CNS of CBA/Ca mice after day 52 of infection and only in the lymph nodes of BALB/c mice between days 14 and 21 after infection. Highest levels of IL-I0 were observed in lymph nodes and CNS of infected CBA/Ca mice. Variations in cytokine levels in lymph nodes and CNS of these mouse strains may account for differences in their susceptibility to TE.
Bibliography:Reprints or correspondence: Dr. C. A. Hunter. Research Institute. Palo Alto Medical Foundation. Palo Alto, CA 9430 I.
ark:/67375/HXZ-D4MPTHVS-X
istex:D1C38A363C761D6751D7A2E270A872991962DE02
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0022-1899
1537-6613
DOI:10.1093/infdis/170.4.939