Publication Date |
2005 |
Personal Author |
Mohrs, M.; Blakesppor, C. M.; Wang, Z. E. |
Page Count |
34 |
Abstract |
Mechanisms underlying the differentiation of stable T helper subsets will be important in understanding how discrete types of immunity develop in response to different pathogens. An evolutionarily conserved approx. 400 base pair non-coding sequence in the IL- 4/IL-13 intergenic region, designated CNS-1, was deleted in mice. The capacity to develop Th2 cells was compromised in vitro and in vivo in the absence of CNS-1. Despite the profound effect in T cells, mast cells from CNS-1-deleted mice maintained their capacity to produce IL-4. A T cell-specific element critical for optimal expression of type 2 cytokines may represent evolution of a regulatory sequence exploited by adaptive immunity. |
Keywords |
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Source Agency |
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Corporate Authors |
California Univ., San Francisco.; Department of Energy, Washington, DC.; Lawrence Berkeley National Lab., CA. Earth Sciences Division. |
Supplemental Notes |
Prepared in cooperation with Lawrence Berkeley National Lab., CA. Earth Sciences Division. Sponsored by Department of Energy, Washington, DC. |
Document Type |
Technical Report |
NTIS Issue Number |
200520 |