Parasite-induced IL-12 stimulates early IFN-gamma synthesis and resistance during acute infection with Toxoplasma gondii.
about
Regulation of adaptive immunity; the role of interleukin-10Disruption of Toxoplasma gondii parasitophorous vacuoles by the mouse p47-resistance GTPases.Immune response and immunopathology during toxoplasmosisPassage of parasites across the blood-brain barrierIn vivo microbial stimulation induces rapid CD40 ligand-independent production of interleukin 12 by dendritic cells and their redistribution to T cell areasPathogen-specific loss of host resistance in mice lacking the IFN-gamma-inducible gene IGTPUse and abuse of dendritic cells by Toxoplasma gondiiInterferon-gamma- and perforin-mediated immune responses for resistance against Toxoplasma gondii in the brainRole of interleukin-10 in malaria: focusing on coinfection with lethal and nonlethal murine malaria parasitesToxoplasma gondii soluble tachyzoite antigen triggers protective mechanisms against fatal intestinal pathology in oral infection of C57BL/6 miceUNC93B1 mediates host resistance to infection with Toxoplasma gondiiDynamic Imaging of CD8(+) T cells and dendritic cells during infection with Toxoplasma gondiiChitinase dependent control of protozoan cyst burden in the brainMIF Promotes Classical Activation and Conversion of Inflammatory Ly6C(high) Monocytes into TipDCs during Murine Toxoplasmosis.Glycyrrhizin enhances interleukin-12 production in peritoneal macrophagesInterleukin 12 a key immunoregulatory cytokine in infection applicationsRecognition of Toxoplasma gondii by TLR11 prevents parasite-induced immunopathologyCD11c-Expressing Cells Affect Regulatory T Cell Behavior in the Meninges during Central Nervous System Infection.Regulation of immunopathogenesis during Plasmodium and Toxoplasma infections: more parallels than distinctions?Toxoplasma gondii upregulates interleukin-12 to prevent Plasmodium berghei-induced experimental cerebral malaria.Early NK cell-derived IFN-{gamma} is essential to host defense in neutropenic invasive aspergillosis.The protein kinase double-stranded RNA-dependent (PKR) enhances protection against disease cause by a non-viral pathogen.Immunological interactions between 2 common pathogens, Th1-inducing protozoan Toxoplasma gondii and the Th2-inducing helminth Fasciola hepaticaDifferential regulation of effector- and central-memory responses to Toxoplasma gondii Infection by IL-12 revealed by tracking of Tgd057-specific CD8+ T cells.Recombinant TgHSP70 Immunization Protects against Toxoplasma gondii Brain Cyst Formation by Enhancing Inducible Nitric Oxide Expression.GRA25 is a novel virulence factor of Toxoplasma gondii and influences the host immune responseProtection against lethal Neospora caninum infection in mice induced by heterologous vaccination with a mic1 mic3 knockout Toxoplasma gondii strain.Decrease of Foxp3+ Treg cell number and acquisition of effector cell phenotype during lethal infectionThe CD8 T-cell road to immunotherapy of toxoplasmosis.A dichotomous role for nitric oxide during acute Toxoplasma gondii infection in miceIn vivo regulation of replicative Legionella pneumophila lung infection by endogenous interleukin-12.Toxoplasma gondii triggers granulocyte-dependent cytokine-mediated lethal shock in D-galactosamine-sensitized mice.Acute and chronic phases of Toxoplasma gondii infection in mice modulate the host immune responses.Partially protective vaccination permits the development of latency in a normally virulent strain of Toxoplasma gondii.Murine dendritic cells pulsed in vitro with Toxoplasma gondii antigens induce protective immunity in vivoNF-kappaB1 contributes to T cell-mediated control of Toxoplasma gondii in the CNS.Interleukin-12 (IL-12) and IL-18 are important in innate defense against genital herpes simplex virus type 2 infection in mice but are not required for the development of acquired gamma interferon-mediated protective immunity.IL-10 production by CD4+ effector T cells: a mechanism for self-regulation.NK cells help to induce CD8(+)-T-cell immunity against Toxoplasma gondii in the absence of CD4(+) T cells.Toxoplasma gondii: 25 years and 25 major advances for the field
P2860
Q21131215-15CD8E4F-F3E5-4D45-AB30-37B2036969B8Q22255523-3B2F3E7D-F304-406B-9C3C-04B415BB71E3Q24612341-59CA3969-9B60-401E-A627-E8BB3CC81EA8Q24632132-83AD543D-0540-42B3-B2E4-B62751362172Q24652833-8488DE3F-B9E8-477C-918F-1E5B0A3D50E4Q24679086-ABD83C81-64DF-4A97-A82D-DA60E7A63050Q26852870-68DAF2C9-4D01-4238-A61B-ECF2C4EA7A2FQ27011746-51D83075-5566-4AAC-9D3A-F55DC4251C66Q27021181-9CFD6855-A640-4A3B-B6D5-9D890B14AE8CQ27305548-EA38D7DD-27E2-448B-B751-1E8FFA5CBEBBQ27313711-EB8DCCBB-2C3B-4D8D-8D84-8EBFC29BF40EQ27316619-E5C447FB-D029-4F2D-822E-2D5F2CB90E23Q27341871-E6FBC006-66A0-4ED1-BD60-6361BE451F34Q27348931-BD2E4977-038E-4220-A747-30215F36C901Q28367036-DEBAEFBA-E13D-44F3-B2CC-76F0606EFC1DQ28395500-6CE9C6E1-5590-43AF-B460-2DD9F50CD8CEQ28589947-E400062D-7F14-4FE4-B861-E730385FD7CCQ30252696-C86B14FF-A9E3-4486-ADB6-9AAC425B9B32Q30409386-045B85AB-A629-473C-BC01-29A4A4C3E00AQ30411019-D5E53B53-7C94-4729-991E-D9342BCAAAC6Q30433397-38355AC4-7B1B-4678-A228-471FEEF215EAQ31129671-5C2744F5-BA38-41BB-B2C1-7CEDC67FA3F6Q33455478-6675F954-BA81-4871-912E-8DAA663EE99EQ33545222-54A2F754-7035-41AA-82C7-C7F967370146Q33599823-EC6948DF-5D08-4CD5-A46B-589183155A10Q33602978-99D8BA1E-501A-4C2B-AD40-34C8DE16BAE6Q33613947-A6163521-9B7F-410B-9478-252B0192EF65Q33624096-132597B1-EFBB-4808-9CF2-B9B07C355AF0Q33732215-2D658BC2-051A-4BDA-8A92-624BDB5579B4Q33738007-1460FAD4-F2B9-4047-B232-1D39493AA4E2Q33747346-C1D020B5-418F-4347-A637-C731C15ECEDAQ33752033-7DAA5C7E-3675-489F-94F2-0316887F5020Q33755653-E89ED67E-2622-4AD8-AB92-E7CFBC455B95Q33762617-857B080C-7989-4689-BE39-BBE103C5FBF3Q33765923-EE77C093-B610-4D95-A248-E2AE56EFF1B7Q33814730-D98843DE-E8B2-4541-976E-EF52D9E80715Q33843902-17A14D5F-8490-499B-B812-5C5CD3B94EB9Q33927028-1C27A9B8-B3DB-4DFD-9AA3-210FFDF2DDCFQ33946628-082CD490-92F3-4D2E-8B30-B1AB86E98350Q33956789-1C57B998-1854-49B4-B857-F2A7E9752599
P2860
Parasite-induced IL-12 stimulates early IFN-gamma synthesis and resistance during acute infection with Toxoplasma gondii.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年学术文章
@wuu
1994年学术文章
@zh-cn
1994年学术文章
@zh-hans
1994年学术文章
@zh-my
1994年学术文章
@zh-sg
1994年學術文章
@yue
1994年學術文章
@zh
1994年學術文章
@zh-hant
name
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@en
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@nl
type
label
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@en
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@nl
prefLabel
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@en
Parasite-induced IL-12 stimula ...... ection with Toxoplasma gondii.
@nl
P2093
P1476
Parasite-induced IL-12 stimula ...... fection with Toxoplasma gondii
@en
P2093
Denkers EY
Gazzinelli RT
Trinchieri G
P304
P407
P577
1994-09-01T00:00:00Z