Clonal expansion of T cells infiltrating in the airways of non-atopic asthmatics
Article first published online: 24 DEC 2001
DOI: 10.1046/j.1365-2249.2000.01148.x
Additional Information
How to Cite
Umibe, T., Kita, Y., Nakao, A., Nakajima, H., Fukuda, T., Yoshida, S., Sakamaki, T., Saito, Y. and Iwamoto, I. (2000), Clonal expansion of T cells infiltrating in the airways of non-atopic asthmatics. Clinical & Experimental Immunology, 119: 390–397. doi: 10.1046/j.1365-2249.2000.01148.x
Publication History
- Issue published online: 24 DEC 2001
- Article first published online: 24 DEC 2001
- Abstract
- Article
- References
- Cited By
Keywords:
- non-atopic asthma;
- bronchoalveolar lavage fluids;
- T cell receptor Vβ genes;
- single-strand conformation polymorphism;
- CDR3
CD4+ T cells are thought to play an important role in airway inflammation in both atopic and non-atopic asthma. However, the mechanism by which T cells are activated in non-atopic asthma, where there is no causative antigen identified, is unknown. To elucidate this issue, we analysed T cell receptor (TCR) Vβ gene clonotypes of T cells in the bronchoalveolar lavage fluids (BALF) of non-atopic asthmatics using polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP) analysis and a sequencing method. We found that the numbers of TCR Vβ gene clonotypes of T cells in the BALF of non-atopic asthmatics were significantly increased compared with those of peripheral blood lymphocytes (PBL). We also found that there were several shared amino acid motifs in complementarity-determining region 3 (CDR3) of TCR Vβ genes from those T cell clones in BALF of non-atopic asthmatics, whereas these shared motifs were not found in the same Vβ family genes from PBL in the patients. Moreover, a conserved amino acid sequence was detected in two patients who shared a common HLA-DR allele. These results indicate that the infiltrating T cells in the airways of non-atopic asthmatics recognize relatively limited epitopes of antigens and are clonally expanded by antigen-driven stimulation.

1365-2249/asset/cei_left.gif?v=1&s=ffee144c532fe5e73bbb89290ba14e154b0d400b)
1365-2249/asset/cei_right.gif?v=1&s=c14d545a5215173707c8202758d5b25fd0bede44)
1365-2249/asset/cover.gif?v=1&s=d4467d7f3170476372896b9f36344ab40422bf6f)