Abstract
Immunoglobulins drive efficient antigen capture by antigen presenting calls for processing and presentation on class II MHC-molecules. High affinity antibody/antigen interactions are stable at endosomal/lysosomal pH thus altering the substrate for antigen processing. We show that this can result in strong suppression of presentation of some T cell epitopes. This effect was observed when the antibody specificity was a B call surface Ig, or formed part of an immune complex. In the latter case the presence of the suppressing antibody boosts presentation of other T cell epitopes through enhanced uptake into Fc receptor bearing cells. The influence of bound antibodies on the outcome of antigen processing may influence with T cell epitopes dominate T cell responses and may change the focus of the response with time.
Original language | English |
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Pages (from-to) | 1459-1463 |
Number of pages | 5 |
Journal | Journal of Experimental Medicine |
Volume | 178 |
Issue number | 4 |
DOIs | |
Publication status | Published - 1 Oct 1993 |
ASJC Scopus subject areas
- General Medicine