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...
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Published in: | The Journal of infectious diseases Vol. 170; no. 4; pp. 939 - 945 |
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The University of Chicago Press
01-10-1994
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Abstract | 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. |
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AbstractList | 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-gamma (IFN-gamma) and tumor necrosis factor (TNF) in lymph nodes of both strains on day 7 of infection, with elevated levels of IFN-gamma 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-10 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. 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. 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-γ (IFN-γ) and tumor necrosis factor (TNF) in lymph nodes of both strains on day 7 of infection, with elevated levels of IFN-γ 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-10 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. |
Author | Remington, J. S. Litton, M. J. Hunter, c. A. Abrams, J. S. |
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Notes | 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 |
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Snippet | BALB/c mice develop toxoplasmic encephalitis (TE) but the pathology resolves; in contrast, CBA/Ca mice develop progressive TE. Immunohistochemical analysis... |
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SubjectTerms | Animals Brain - immunology Brain - pathology Central nervous system Cytokines Disease Susceptibility Encephalitis Female Immunity, Innate Immunohistochemistry - methods Infections Interferon-gamma - analysis Interferon-gamma - physiology Interleukins Lymph nodes Lymph Nodes - immunology Lymph Nodes - pathology Major Article Mice Mice, Inbred BALB C Mice, Inbred CBA Species Specificity T lymphocytes Toxoplasmosis Toxoplasmosis, Cerebral - immunology Toxoplasmosis, Cerebral - pathology Tumor Necrosis Factor-alpha - analysis Tumor Necrosis Factor-alpha - physiology Tumor necrosis factors |
Title | Immunocytochemical Detection Of Cytokines In The Lymph Nodes And Brains Of Mice Resistant Or Susceptible To Toxoplasmic Encephalitis |
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