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Cutting Edge: Lack of High Affinity Competition for Peptide in Polyclonal CD4+ Responses Unmasks IL-4 Production
被引:50
|作者:
Milner, Joshua D.
[1
,2
]
Fazilleau, Nicolas
[3
]
McHeyzer-Williams, Michael
[3
]
Paul, William
[1
]
机构:
[1] NIAID, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] NIAID, Lab Allerg Dis, NIH, Bethesda, MD 20892 USA
[3] Scripps Res Inst, La Jolla, CA 92037 USA
基金:
美国国家卫生研究院;
关键词:
T-CELLS;
ANTIGEN;
DIFFERENTIATION;
SELECTION;
INFANTS;
LIGANDS;
D O I:
10.4049/jimmunol.1000674
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Priming of naive monoclonal CD4 T cells via weak agonsim permits GATA-3 transcription and Th2 differentiation. To test whether this process can occur in polyclonal naive populations, where a range of TCR affinities exists for any given Ag/MHC complex, we primed naive CD4 cells from 5CC7 V beta 3 transgenic mice, which have a fixed beta-chain specific for pigeon cytochrome c peptide I-E-k. Priming populations depleted of higher affinity, moth cytochrome c peptide I-E-k tetramer-binding cells resulted in substantial IL-4 production that did not occur in the presence of higher affinity cells. TCR alpha-chain sequence analysis showed that clones that possessed TCR features associated with high affinity responses to pigeon cytochrome c made less IL-4 than clones that possessed fewer such motifs. These results indicate that cells bearing TCRs that are weakly stimulated by their cognate Ag preferentially adopt a Th2 phenotype when primed in the absence of competition from cells with higher affinity receptors. The Journal of Immunology, 2010, 184: 6569-6573.
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页码:6569 / 6573
页数:5
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