Abstract
Interferon-γ (IFNγ) is essential for preventing reactivation of chronic infection with Toxoplasma gondii in the brain. We examined the role of IFNγ on lymphocyte and endothelial adhesion molecule expression and T cell recruitment into the brain during chronic infection with T. gondii in IFNγ knockout (IFNγ −/−) and wild-type (WT) mice. Although the number of cerebral vessels expressing intercellular adhesion molecule-1 (ICAM-1) and vascular cell adhesion molecule-1 (VCAM-1) increased in both WT and IFNγ −/− mice following infection, there were more VCAM-1+ vessels in brains of infected WT than of infected IFNγ −/− mice; in contrast, numbers of ICAM-1+ vessels did not differ between strains. We did not detect endothelial E-selectin, P-selectin, MAdCAM-1, or PNAd in any of the brains. Significantly fewer CD8+ T cells were recruited into brains of infected IFNγ −/− than WT mice. Treatment of infected IFNγ −/− mice with recombinant IFN-γ restored the expression of VCAM-1 on their cerebral vessels and recruitment of CD8+ T cells into their brains, confirming an importance of this cytokine for upregulation of VCAM-1 expression and CD8+ T cell trafficking. In infected WT and IFNγ −/− animals, almost all cerebral CD8+ T cells were lymphocyte function-associated antigen-1 (LFA-1)high, CD44high, and CD62Lneg, and approximately 38% were α4β1 integrin+. In adoptive transfer of immune spleen cells, pretreatment of the cells with a monoclonal antibody (mAb) against α4 integrin markedly inhibited recruitment of CD8+ T cells into the brain of chronically infected WT mice. These results indicate that IFN-γ-induced expression of endothelial VCAM-1 and its binding to α4β1 integrin on CD8+ T cells is important for recruitment of the T cells into the brain during the chronic stage of T. gondii infection, although LFA-1/ICAM-1 interaction may also be involved in this process.
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