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
AUTHORS (5)
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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