4.2 Article

T cell-derived interferon-γ is required for host defense to Toxoplasma gondii

期刊

PARASITOLOGY INTERNATIONAL
卷 75, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.parint.2019.102049

关键词

interferon-gamma; Toxoplasma gondii; GREVEN mice; CD4(+) T cells; CD8(+) T cells

资金

  1. Research Program on Emerging and Re-emerging Infectious Diseases from Agency for Medical Research and Development (AMED) [JP19fk0108047]
  2. Japanese Initiative for Progress of Research on Infectious Diseases for global Epidemic from Agency for Medical Research and Development (AMED) [JP19fm0208018]
  3. Strategic International Collaborative Research Program from Agency for Medical Research and Development (AMED) [19jm0210067h]
  4. Ministry of Education, Culture, Sports, Science and Technology [19H04809, 18KK0226, 18H02642, 19H00970]
  5. Cooperative Research Grant of the Institute for Enzyme Research, Joint Usage/Research Center, Tokushima University
  6. Takeda Science Foundation
  7. Mochida Memorial Foundation on Medical and Pharmaceutical Research
  8. Uehara Memorial Foundation
  9. Naito Foundation
  10. Astellas Foundation for Research on Metabolic Disorders
  11. Research Foundation for Microbial Diseases of Osaka University
  12. Grants-in-Aid for Scientific Research [19H00970, 19H04809, 18H02642, 18KK0226] Funding Source: KAKEN

向作者/读者索取更多资源

Interferon-gamma (IFN-gamma) is important for host defense against various intracellular organisms including a protozoan pathogen Toxoplasma gondii. Various immune cells are recently shown to produce IFN-gamma in T. gondii infection, however, it remains elusive which cell types are important for anti-T. gondii host defense so far. Here we generate a new IFN-gamma reporter GREVEN mouse line in which a fusion protein of Venus and NanoLuc to analyze IFN-gamma producing cells during T. gondii infection and find that CD4(+), CD8(+), gamma delta T cells and natural killer cells express Venus in a time dependent manner. Furthermore, Lck-Cre/Ifng(fl/fl) mice are highly susceptible to T. gondii infection. Taken together, our results demonstrate that T cell-derived IFN-gamma plays an important role in anti-T. gondii host defense.

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