Der p I, a major allergen of the house dust mite, proteolytically cleaves the low‐affinity receptor for human IgE (CD23)

O Schulz, P Laing, HF Sewell… - European journal of …, 1995 - Wiley Online Library
O Schulz, P Laing, HF Sewell, F Shakib
European journal of immunology, 1995Wiley Online Library
The nature of the proteases that cleave CD23 in vivo is of considerable interest, but remains
unknown. Here, we demonstrate that Der p I, a major allergen of the house dust mite
Dermatophagoides pteronyssinus, cleaves CD23 from the surface of cultured human B cells
(RPMI 8866 B cell line). The cleavage of the receptor from the B cell surface was associated
with a parallel increase in soluble CD23 (sCD23) in the culture supernatant. Furthermore,
the proteolytic effect of Der p I was specific for CD23, since none of the other B cell markers …
Abstract
The nature of the proteases that cleave CD23 in vivo is of considerable interest, but remains unknown. Here, we demonstrate that Der p I, a major allergen of the house dust mite Dermatophagoides pteronyssinus, cleaves CD23 from the surface of cultured human B cells (RPMI 8866 B cell line). The cleavage of the receptor from the B cell surface was associated with a parallel increase in soluble CD23 (sCD23) in the culture supernatant. Furthermore, the proteolytic effect of Der p I was specific for CD23, since none of the other B cell markers tested (CD20, HLA-DR, CD71 and CD49d) were affected. Labeled antibody experiments and protease inhibition assays clearly demonstrate that Der p I is a cysteine protease that directly cleaves a 25-kDa fragment of CD23. These data suggest that the cysteine protease Der p I, in addition to being highly immunogenic, may up-regulate IgE synthesis by virtue of its ability to cleave CD23.
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