Differential role of CD80 and CD86 on alveolar macrophages in the presentation of allergen to T lymphocytes in asthma

Authors

  • P. Balbo,

    1. San Raffaele Scientific Institute, Milan, *Chair of Respiratory Physiology, University of Genoa and †G. Gaslini Scientific Institute, Genoa, and ‡AOR 11, Ospedale di Cattinara, Vercelli, Italy
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  • M. Silvestri,

    1. San Raffaele Scientific Institute, Milan, *Chair of Respiratory Physiology, University of Genoa and †G. Gaslini Scientific Institute, Genoa, and ‡AOR 11, Ospedale di Cattinara, Vercelli, Italy
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  • G. A. Rossi,

    1. San Raffaele Scientific Institute, Milan, *Chair of Respiratory Physiology, University of Genoa and †G. Gaslini Scientific Institute, Genoa, and ‡AOR 11, Ospedale di Cattinara, Vercelli, Italy
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  • E. Crimi,

    1. San Raffaele Scientific Institute, Milan, *Chair of Respiratory Physiology, University of Genoa and †G. Gaslini Scientific Institute, Genoa, and ‡AOR 11, Ospedale di Cattinara, Vercelli, Italy
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  • S. E. Burastero

    1. San Raffaele Scientific Institute, Milan, *Chair of Respiratory Physiology, University of Genoa and †G. Gaslini Scientific Institute, Genoa, and ‡AOR 11, Ospedale di Cattinara, Vercelli, Italy
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Samuele E. Burastero MD, Department of Biological and Technological Research, San Raffaele Scientific Institute, Via Olgettina 58, 20132 Milano, Italy. E-mail: burastero.samuele@hsr.it

Abstract

In the asthmatic lung the altered expression of costimulatory molecules (CD80, CD86) by alveolar macrophages contributes to T lymphocyte activation and expansion. We hypothesized that CD80 and CD86 on alveolar macrophages could differentially support allergic inflammation in adult asthma. Here we studied 11 subjects with mild allergic asthma and 11 atopic non-asthmatics as controls. Dermatophagoides-specific T cell lines were derived from peripheral blood from each subject. Bronchoalveolar lavage with evaluation of lung inflammatory cells was performed in all individuals at baseline and 24 h after allergen challenge. The expression of CD80 and CD86 costimulatory molecules by alveolar macrophages was studied and, in parallel, the efficiency of antigen presentation was measured in terms of IL-4 and IL-5 production by allergen-stimulated autologous T cells. We found that in asthmatic subjects (i) the percent of CD80+, but not CD86+ alveolar macrophages was increased at baseline and did not change following allergen challenge; (ii) CD86, but not CD80, membrane expression was up-regulated following allergen challenge; (iii) both CD80 and CD86 were required to support Th2 cytokine production by allergen-specific T cells, with a prevalent role of CD86 after allergen challenge. Our data indicate that alveolar macrophages deliver costimulatory signals via CD80 and CD86, which support the production of Th2 cytokines by allergen-specific T cells. They also indicate that CD86 in vivo is up-regulated in the 24 h following allergen exposure and that this modulation is functionally relevant.

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