Vβ8+ T lymphocytes are essential in the regulation of airway hyperresponsiveness and bronchoalveolar eosinophilia but not in allergen-specific IgE in a murine model of allergic asthma

被引:0
作者
Hofstra, CL
Van Ark, I
Savelkoul, HFJ
Cruikshank, WW
Nijkamp, FP
Van Oosterhout, AJM
机构
[1] Univ Utrecht, Dept Pharmacol & Pathophysiol, NL-3508 TB Utrecht, Netherlands
[2] Erasmus Univ, Dept Immunol, NL-3000 DR Rotterdam, Netherlands
[3] Boston Univ, Sch Med, Ctr Pulm, Boston, MA 02118 USA
关键词
mouse; T lymphocytes; eosinophils; IgE; airway hyperresponsiveness;
D O I
暂无
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background There is increasing evidence that in allergic asthma the inflammatory process is regulated by T lymphocytes. In BALB/c mice the majority of ovalbumin responsive T lymphocytes express the V beta 8.1(+) and V beta 8.2(+) T-cell receptor. Objective We analysed the contribution of V beta 8(+) T lymphocytes during the sensitization and challenge phase in the regulation of antigen-specific IgE, airway hyperresponsiveness and cellular infiltration in the airways in a murine model of allergic asthma. Methods Mice strains genetically lacking (SJL/J and SJA/9) and expressing (BALB/c) the V beta 8(+) T cell receptor were used. In addition, prior to the sensitization and prior to the challenge BALB/c mice were treated with antibodies to V beta 8. Mice were sensitized with ovalbumin, followed by repeated challenge with ovalbumin or saline aerosols. Results In ovalbumin challenged BALB/c mice treated with control antibody a significant increase in eosinophils in the bronchoalveolar lavage, airway hyperresponsiveness and increased serum levels of ovalbumin-specific IgE were observed compared to control mice. Treatment of BALB/c mice with antibodies to V beta 8 prior to the sensitization or prior to the challenge period completely inhibited the ovalbumin induced infiltration of eosinophils and airway hyperresponsiveness, while ovalbumin-specific IEE was slightly decreased. In SJA/9 and SJL/J mice ovalbumin challenge did not induce eosinophilic infiltration and airway hyperresponsiveness. In SJL/J mice ovalbumin challenge induced an upregulation of ovalbumin-specific IgE, however, in SJA/9 mice no upregulation was observed. Conclusion It is demonstrated that V beta 8(+) T lymphocytes are essential for infiltration of eosinophils in the airways and development of airway hyperresponsiveness in a murine model of allergic asthma. In contrast, although V beta 8(+) T lymphocytes seem to be important for the extent of IgE levels, no essential role for V beta 8(+) T lymphocytes in the induction of antigen-specific IgE was observed.
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页码:1571 / 1580
页数:10
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