| JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY | 卷:104 |
| Mast cell-T cell interactions | |
| Article | |
| Mekori, YA ; Metcalfe, DD | |
| 关键词: mast cell; T cell; adhesion; antigen presentation; chemotaxis; cytokines; degranulation; migration; | |
| DOI : 10.1016/S0091-6749(99)70316-7 | |
| 来源: Elsevier | |
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【 摘 要 】
In addition to being a major effector cell in the elicitation of allergic inflammation, mast cells have been found to be activated in various T cell-mediated inflammatory processes and to reside in close physical proximity to T cells, Such observations and the wide spectrum of mediators produced and secreted by mast cells have led investigators to propose a functional relationship between these 2 cell populations. Indeed, mast cell activation has been reported to induce T-cell migration either directly by the release of chemotactic factors, such as lymphotactin or IL-16, or indirectly by the induction of adhesion molecule expression on endothelial cells, Mast cells are also able to present antigens to T cells, resulting in their activation in either an MHC class I- or class II-restricted and costimulatory molecule-dependent fashion. Adhesion molecule-dependent intercellular contact or MHC class II cognate interactions between T cells and mast cells result in the release of both granule-associated mediators and cytokines from the latter, Also, T cell-derived mediators, such as beta-chemokines, directly induce mast cell degranulation, On the other hand, mast cell-derived cytokines, such as IL-4, have been found to polarize T cells to preferentially differentiate into the T-H2 subset. Thus T cell-mast fell interactions are bidirectional, fulfilling regulatory and/or modulatory roles affecting various aspects of the immune response.
【 授权许可】
Free
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 10_1016_S0091-6749(99)70316-7.pdf | 120KB |
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