Abstract
Inflammation induced during infection can both promote and suppress immunity. This contradiction suggests that inflammatory cytokines affect the immune system in a context-dependent manner. Here we show that nonspecific bystander inflammation conditions naive CD4(+) T cells for enhanced peripheral Foxp3 induction and reduced effector differentiation. This results in inhibition of immune responses in vivo via a Foxp3-dependent effect on antigen-specific naive CD4(+) T cell precursors. Such conditioning may have evolved to allow immunity to infection while limiting subsequent autoimmunity caused by release of self-antigens in the wake of infection. Furthermore, this phenomenon suggests a mechanistic explanation for the idea that early tuning of the immune system by infection affects the long-term quality of immune regulation.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Asthma / immunology*
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Autoantigens
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Autoimmunity / immunology*
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Bystander Effect / drug effects
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Bystander Effect / immunology*
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CD4-Positive T-Lymphocytes / drug effects
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CD4-Positive T-Lymphocytes / immunology*
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Cell Line, Tumor
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Cytokines / drug effects
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Cytokines / immunology*
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Cytokines / pharmacology
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DNA Methylation
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Diabetes Mellitus / immunology*
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Disease Models, Animal
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Female
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Flow Cytometry
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Forkhead Transcription Factors / genetics
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Forkhead Transcription Factors / immunology*
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Gene Expression Profiling
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Inflammation*
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Interferon Inducers / pharmacology
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Male
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Mice
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Mice, Inbred BALB C
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Mice, Inbred C57BL
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Mice, Transgenic
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Peripheral Tolerance / immunology
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Poly I-C / pharmacology
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Promoter Regions, Genetic
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Self Tolerance / immunology*
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Thymic Stromal Lymphopoietin
Substances
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Autoantigens
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Cytokines
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Forkhead Transcription Factors
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Foxp3 protein, mouse
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Interferon Inducers
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Poly I-C
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Thymic Stromal Lymphopoietin
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TSLP protein, mouse