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. 2005 Jul;141(1):122-9.
doi: 10.1111/j.1365-2249.2005.02815.x.

Increased expression of plasma and cell surface co-stimulatory molecules CTLA-4, CD28 and CD86 in adult patients with allergic asthma

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Increased expression of plasma and cell surface co-stimulatory molecules CTLA-4, CD28 and CD86 in adult patients with allergic asthma

C K Wong et al. Clin Exp Immunol. 2005 Jul.

Abstract

The co-stimulatory interactions of the B7 family molecules CD80 and CD86 on antigen-presenting cells, together with their T cell counter receptors CD28 and cytotoxic T lymphocyte-associated antigen-4 (CTLA-4), modulate T lymphocyte-mediated immune responses in a reciprocal manner. To investigate whether there is altered expression and the clinical significance of soluble co-stimulatory molecules in asthmatic patients, plasma concentrations of sCTLA-4, sCD28, sCD80 and sCD86 in 51 adult allergic asthmatic adults with or without steroid treatment, and 35 sex- and age-matched control subjects were measured by enzyme-linked immunosorbent assay (ELISA). Cell surface expression of CTLA-4 and CD28 on peripheral blood mononuclear cells (PBMC) were analysed by flow cytometry. Results showed that the plasma sCTLA-4 concentration was significantly higher in all asthmatic patients while sCD28 and sCD86 concentrations were significantly higher in steroid and non-steroid treated asthmatic patients, respectively, compared with control subjects (all P < 0.01). Significantly increased cell surface expression of CD28 but not CTLA-4 on PBMC was found in asthmatic patients compared with controls (P < 0.05). The plasma concentration and cell surface expression of CTLA-4 were found to exhibit positive and significant correlations with those of CD28 (both P < 0.05). Serum total IgE concentration correlated positively and significantly with sCTLA-4 and sCD28 concentrations in allergic asthmatic patients (both P < 0.05). The increased expression of these soluble co-stimulatory molecules may reflect the dysregulation of T cell activation, thereby contributing to the immunopathogenesis of allergic asthma.

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Figures

Fig. 1
Fig. 1
Scatter-plots of plasma concentrations of (a), sCTLA-4 (b) sCD28, (c) sCD80 and (d) sCD86 of control subjects, non-steroid-treated and steroid-treated asthmatic patients. The differences between asthmatic patients and control subjects were determined by non-parametric Mann–Whitney rank sum test. *P < 0·05, **P < 0·01, ***P < 0·001.
Fig. 2
Fig. 2
The percentage cell surface expression of (a) CTLA-4 and (b) CD28 on peripheral blood mononuclear cells (PBMC) of control subjects, non-steroid-treated asthma subjects and steroid-treated asthmatic patients. The differences between asthmatic patients and control subjects were determined by non-parametric Mann–Whitney rank sum test. *P < 0·05, **P < 0·01.

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References

    1. Marone G. Asthma: recent advances. Immunol Today. 1998;19:5–9. - PubMed
    1. Larche M, Robinson DS, Kay AB. The role of T lymphocytes in the pathogenesis of asthma. J Allergy Clin Immunol. 2003;111:450–63. - PubMed
    1. Chambers CA, Allison JP. Co-stimulation in T cell responses. Curr Opin Immunol. 1997;9:396–404. - PubMed
    1. Greenfield EA, Nguyen KA, Kuchroo VK. CD28/B7 co-stimulation: a review. Crit Rev Immunol. 1998;18:389–418. - PubMed
    1. Linsley PS, Clark EA, Ledbetter JA. T-cell antigen CD28 mediates adhesion with B cells by interacting with activation antigen B7/BB-1. Proc Natl Acad Sci USA. 1990;87:5031–5. - PMC - PubMed

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