Abstract |
The cellular inflammatory responses which are seen in allergic and asthmatic diseases are viewed as being quite strongly dependent on the activities of T cells and their products. The major T cell subset involved appears to be the so-called CD4+ Th2 subset which produces interleukin-4 (IL-4) and interleukin-5 (IL-5). In vitro and in vivo experiments have indicated that IL-4 is a key regulator in these kinds of immune responses, not only switching B cells to IgE production, but acting on CD4+ T cells to drive their development towards a Th2 phenotype. Recent results have shown that the functional phenotype of CD8+ T cells can be switched from interferon gamma production to IL-4 and IL-5 production by the presence of IL-4. This could prove an especially important phenomenon since it is the production of interferon gamma by CD8 T cells which is seen as necessary for protection against virus infection. This short review updates our current knowledge of how IL-4 can act on CD4+ and CD8+ T cell subsets in in vivo models of asthma and allergic disease.
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Authors | K J Erb, G Le Gros |
Journal | Immunology and cell biology
(Immunol Cell Biol)
Vol. 74
Issue 2
Pg. 206-8
(Apr 1996)
ISSN: 0818-9641 [Print] United States |
PMID | 8724011
(Publication Type: Journal Article, Review)
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Chemical References |
- Interleukin-5
- Interleukin-4
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Topics |
- Animals
- Asthma
(immunology)
- CD4-Positive T-Lymphocytes
(immunology)
- CD8-Positive T-Lymphocytes
(immunology)
- Humans
- Hypersensitivity
(immunology)
- Interleukin-4
(immunology)
- Interleukin-5
(immunology)
- Th2 Cells
(immunology)
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