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IL-33 promotes innate lymphoid cell-dependent IFN-γ production required for innate immunity to Toxoplasma gondii
by
Radaelli, Enrico
, Hunter, Christopher A
, Christian, David A
, Gullicksrud, Jodi A
, Clark, Joseph T
, Tarrant, James C
, Park, Jeongho
, Jacquet, Maxime
, Silver, Jonathan
, Perry, Joseph A
in
Animals
/ Biopsy
/ Cytokines
/ Female
/ Humans
/ IL-1 family
/ IL-33
/ Immunity, Innate
/ Immunology and Inflammation
/ Infections
/ Inflammation
/ Innate immunity
/ innate lymphoid cells
/ Interferon-gamma - genetics
/ Interferon-gamma - immunology
/ Interleukin 12
/ Interleukin-33 - genetics
/ Interleukin-33 - immunology
/ Lymphocytes
/ Lymphocytes - immunology
/ Lymphoid cells
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Microbiology and Infectious Disease
/ Monocytes
/ Parasite resistance
/ Parasites
/ Parasitic diseases
/ RAG1 protein
/ Replication
/ Toxoplasma - genetics
/ Toxoplasma - immunology
/ Toxoplasma gondii
/ Toxoplasmosis - genetics
/ Toxoplasmosis - immunology
/ Toxoplasmosis - parasitology
/ γ-Interferon
2021
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IL-33 promotes innate lymphoid cell-dependent IFN-γ production required for innate immunity to Toxoplasma gondii
by
Radaelli, Enrico
, Hunter, Christopher A
, Christian, David A
, Gullicksrud, Jodi A
, Clark, Joseph T
, Tarrant, James C
, Park, Jeongho
, Jacquet, Maxime
, Silver, Jonathan
, Perry, Joseph A
in
Animals
/ Biopsy
/ Cytokines
/ Female
/ Humans
/ IL-1 family
/ IL-33
/ Immunity, Innate
/ Immunology and Inflammation
/ Infections
/ Inflammation
/ Innate immunity
/ innate lymphoid cells
/ Interferon-gamma - genetics
/ Interferon-gamma - immunology
/ Interleukin 12
/ Interleukin-33 - genetics
/ Interleukin-33 - immunology
/ Lymphocytes
/ Lymphocytes - immunology
/ Lymphoid cells
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Microbiology and Infectious Disease
/ Monocytes
/ Parasite resistance
/ Parasites
/ Parasitic diseases
/ RAG1 protein
/ Replication
/ Toxoplasma - genetics
/ Toxoplasma - immunology
/ Toxoplasma gondii
/ Toxoplasmosis - genetics
/ Toxoplasmosis - immunology
/ Toxoplasmosis - parasitology
/ γ-Interferon
2021
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IL-33 promotes innate lymphoid cell-dependent IFN-γ production required for innate immunity to Toxoplasma gondii
by
Radaelli, Enrico
, Hunter, Christopher A
, Christian, David A
, Gullicksrud, Jodi A
, Clark, Joseph T
, Tarrant, James C
, Park, Jeongho
, Jacquet, Maxime
, Silver, Jonathan
, Perry, Joseph A
in
Animals
/ Biopsy
/ Cytokines
/ Female
/ Humans
/ IL-1 family
/ IL-33
/ Immunity, Innate
/ Immunology and Inflammation
/ Infections
/ Inflammation
/ Innate immunity
/ innate lymphoid cells
/ Interferon-gamma - genetics
/ Interferon-gamma - immunology
/ Interleukin 12
/ Interleukin-33 - genetics
/ Interleukin-33 - immunology
/ Lymphocytes
/ Lymphocytes - immunology
/ Lymphoid cells
/ Male
/ Mice
/ Mice, Inbred C57BL
/ Mice, Knockout
/ Microbiology and Infectious Disease
/ Monocytes
/ Parasite resistance
/ Parasites
/ Parasitic diseases
/ RAG1 protein
/ Replication
/ Toxoplasma - genetics
/ Toxoplasma - immunology
/ Toxoplasma gondii
/ Toxoplasmosis - genetics
/ Toxoplasmosis - immunology
/ Toxoplasmosis - parasitology
/ γ-Interferon
2021
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IL-33 promotes innate lymphoid cell-dependent IFN-γ production required for innate immunity to Toxoplasma gondii
Journal Article
IL-33 promotes innate lymphoid cell-dependent IFN-γ production required for innate immunity to Toxoplasma gondii
2021
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Overview
IL-33 is an alarmin required for resistance to the parasite Toxoplasma gondii , but its role in innate resistance to this organism is unclear. Infection with T. gondii promotes increased stromal cell expression of IL-33, and levels of parasite replication correlate with release of IL-33 in affected tissues. In response to infection, a subset of innate lymphoid cells (ILC) emerges composed of IL-33R + NK cells and ILC1s. In Rag1 −/− mice, where NK cells and ILC1 production of IFN-γ mediate innate resistance to T. gondii , the loss of the IL-33R resulted in reduced ILC responses and increased parasite replication. Furthermore, administration of IL-33 to Rag1 −/− mice resulted in a marked decrease in parasite burden, increased production of IFN-γ, and the recruitment and expansion of inflammatory monocytes associated with parasite control. These protective effects of exogenous IL-33 were dependent on endogenous IL-12p40 and the ability of IL-33 to enhance ILC production of IFN-γ. These results highlight that IL-33 synergizes with IL-12 to promote ILC-mediated resistance to T. gondii .
Publisher
eLife Sciences Publications Ltd,eLife Sciences Publications, Ltd
Subject
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