Tim-3 Induces Th2-Biased Immunity and Alternative Macrophage Activation during Schistosoma japonicum Infection

Male 0301 basic medicine Macrophages Immunity CD8-Positive T-Lymphocytes Macrophage Activation Schistosoma japonicum 3. Good health Killer Cells, Natural Mice, Inbred C57BL Mice 03 medical and health sciences Th2 Cells Liver Schistosomiasis japonica Animals Humans Receptors, Virus Hepatitis A Virus Cellular Receptor 2 Spleen
DOI: 10.1128/iai.00517-15 Publication Date: 2015-05-19T02:11:13Z
ABSTRACT
T cell immunoglobulin- and mucin-domain-containing molecule 3 (Tim-3) has been regarded as an important regulatory factor in both adaptive innate immunity. Recently, Tim-3 was reported to be involved Th2-biased immune responses mice infected with Schistosoma japonicum, but the exact mechanism behind involvement of remains unknown. The present study aims understand role response against S. japonicum infection. expression determined by flow cytometry, increased observed on CD4(+) CD8(+) cells, NK1.1(+) CD11b(+) cells from livers japonicum-infected mice. However, level lower spleen than liver, no increase splenic or cells. schistosome-induced upregulation natural killer (NK) accompanied reduced NK numbers vitro vivo. antibody blockade led inducible nitric oxide synthase interleukin-12 (IL-12) mRNA cocultured soluble egg antigen downregulation Arg1 IL-10, which are markers M2 macrophages. In summary, we critical populations, may alternative activation macrophages during
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