Lowering the affinity between antigen and the B cell receptor can enhance antigen presentation
✍ Scribed by Katie Brooks; Andrew M. Knight
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 247 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0014-2980
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The B cell receptor (BCR) enables antigen‐specific B cells to bind, internalize and target antigens for processing into small peptide fragments. These epitopes are then expressed on the plasmamembrane in association with MHC class II molecules for recognition by CD4^+^ T cells. The affinity of the interaction between the BCR and antigen plays an important part in determining T cell epitope generation. In this report we provide evidence that the efficiency of antigen presentation by specific B cells does not need to be directly proportional to antigen/BCR affinity. We show that increased presentation can result from lowering the affinity of the antigen/BCR interaction. This finding suggests a novel mechanism by which B cells can recruit T cell help and obtain survival signals. Activation of these cells may have consequences for the generation of the B cell repertoire.
📜 SIMILAR VOLUMES
The binding of antigens to the B cell antigen receptor (BCR) results in the initiation of signaling cascades and the internalization of the antigens for processing and presentation. Recent studies indicate that antigen binding destabilizes the BCR as a mechanism to down-regulate B cell responses. Tw
## Abstract Dendritic cells (DC) have gained much interest in the field of anticancer vaccine development because of their central function in immune regulation. However, the clinical application of __ex vivo__ cultured DC has significant disadvantages. A vaccine that targets dendritic cells __in v