ASN NEURO · 2011 · 52 citations · 46 references
Veterinary MedicineImmunologyInfectious DiseasesHost-pathogen InteractionsImmunology Of Infectious DiseasesNeuroimmunologyCentral Nervous System InfectionsHost-parasite Immune InteractionsImmunopathology Of Parasitic DiseaseParasitic Disease PathogenesisProtozoan Host-parasite InteractionsT-cell Responses To ParasitesCd4 Positive T CellsCd8 Positive T CellsImmune Cell MigrationLymphocyte MigrationMatrix MetalloproteinasesParasite Chronic InfectionParasite Clearance MechanismsParasite-immune Interactions
Chronic infection with the intracellular protozoan parasite Toxoplasma gondii leads to tissue remodelling in the brain and a continuous requirement for peripheral leucocyte migration within the CNS (central nervous system). In the present study, we investigate the role of MMPs (matrix metalloproteinases) and their inhibitors in T-cell migration into the infected brain. Increased expression of two key molecules, MMP-8 and MMP-10, along with their inhibitor, TIMP-1 (tissue inhibitor of metalloproteinases-1), was observed in the CNS following infection. Analysis of infiltrating lymphocytes demonstrated MMP-8 and -10 production by CD4+ and CD8+ T-cells. In addition, infiltrating T-cells and CNS resident astrocytes increased their expression of TIMP-1 following infection. TIMP-1-deficient mice had a decrease in perivascular accumulation of lymphocyte populations, yet an increase in the proportion of CD4+ T-cells that had trafficked into the CNS. This was accompanied by a reduction in parasite burden in the brain. Taken together, these findings demonstrate a role for MMPs and TIMP-1 in the trafficking of lymphocytes into the CNS during chronic infection in the brain.
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IL-23 promotes tumour incidence and growth
John L. Langowski, Xueqing Zhang, Lingling Wu et al. · Nature · 2006 · 996 citations
Medicine, Immunology, Oncology +12