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1.
Immune Network ; : 48-59, 2017.
Article in English | WPRIM | ID: wpr-30384

ABSTRACT

Complex communities of microorganisms, termed commensal microbiota, inhabit mucosal surfaces and profoundly influence host physiology as well as occurrence of allergic diseases. Perturbing factors such as the mode of delivery, dietary fibers and antibiotics can influence allergic diseases by altering commensal microbiota in affected tissues as well as in intestine. Here, we review current findings on the relationship between commensal microbiota and allergic diseases, and discuss the underlying mechanisms that contribute to the regulation of allergic responses by commensal microbiota.


Subject(s)
Anti-Bacterial Agents , Asthma , Dermatitis, Atopic , Dietary Fiber , Food Hypersensitivity , Hygiene , Intestines , Microbiota , Physiology
2.
Immune Network ; : 81-87, 2004.
Article in Korean | WPRIM | ID: wpr-217516

ABSTRACT

BACKGROUND: In the thymus, developing thymocytes continually interact with thymic epithelial cell components. Self MHC restriction of mature T cells are imposed in the thymus through interaction of immature double positive thymocytes and thymic cortical epithelial cells. The site of negative selection, however, is a matter of debate. Through systemic injection of anti-TCR antibody or antigenic peptides, investigators suggested that most of the negative selection occurs in the thymic cortex. But the requirements for negative selection, i.e cellular counterparts and costimulatory molecules are more available in the medulla or cortico-medullary junction rather than in the thymic cortex. METHODS: The direct and indirect pathways of thymocyte death after systemic anti-TCR antibody injection were separated through several experimental systems. B6 mice were either adrenalectomized or sham-adrenalectomized to evaluate the role of endogenous glucocorticoids from adrenal gland. Role of TNF were evaluated through using TNF receptor double knockout mice. RESULTS: We found that without indirectly acting mediators such as TNF-alpha or corticosteroid, double positive thymocyte death were minimal by systemic injection of anti-TCR antibody in TNF receptor double knockout neonatal mice. Also by analyzing neonatal wild-type mice with adoptively transferred mature T cells, only peripheral activation of mature T cells could induce extensive double positive thymocyte death. CONCLUSION: Thus, systemically injected anti-TCR antibody mediated thymocyte death are mostly induced through indirect pathway.


Subject(s)
Animals , Humans , Mice , Adrenal Cortex Hormones , Adrenal Glands , Epithelial Cells , Glucocorticoids , Mice, Knockout , Peptides , Receptors, Tumor Necrosis Factor , Research Personnel , T-Lymphocytes , Thymocytes , Thymus Gland , Tumor Necrosis Factor-alpha
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