CD23 antibody: How does it regulate the mechanism of immunoglobulin E-mediated allergic reactions?
1. What are the molecular characteristics and expression patterns of CD23 in the immune system?
CD23, as a type II transmembrane protein composed of 321 amino acids, typically exists as trimers on the cell surface. This molecule has two isoforms, CD23a and CD23b, which differ by only a single amino acid in their intracellular domains. CD23a is specifically expressed on B lymphocytes, while CD23b is expressed in various cell types including B cells and epithelial cells. Notably, membrane-bound CD23 can be cleaved by proteases to generate soluble fragments of different molecular weights, and the dynamic balance between soluble and membrane-bound forms plays a crucial regulatory role in its biological functions. Structurally, CD23 belongs to the C-type lectin family and exhibits calcium-dependent activity.
2. What are the characteristics of the interaction mechanism between CD23 and immunoglobulin E?
As a low-affinity receptor for IgE, CD23 binds to the Cε3 and Cε4 domains of IgE molecules. Compared with the high-affinity receptor FcεRI, CD23 has lower monomeric binding affinity for IgE, but its overall binding capacity can be significantly enhanced through oligomerization on the cell surface. This binding property is also influenced by the valency of IgE molecules, with CD23 preferentially capturing IgE-allergen complexes rather than free IgE. Calcium binding induces conformational changes in CD23, further strengthening its interaction with IgE. This sophisticated regulatory mechanism ensures the specific functions of CD23 in immune responses.
3. How does CD23 participate in the regulatory network of IgE synthesis?
Experimental studies have shown that CD23 plays a dual role in IgE synthesis regulation. In transgenic animal models, overexpression of CD23 can suppress the production of allergen-specific IgE after exposure, while CD23-deficient mice exhibit enhanced IgE synthesis. At the molecular level, high concentrations of IgE can stabilize membrane-bound CD23 and inhibit its proteolytic cleavage, forming a negative feedback loop. Conversely, cleavage of CD23 not only weakens its regulatory function but may also lead to abnormally elevated IgE levels. This delicate balance mechanism provides important insights into IgE dysregulation in allergic diseases.
4. What is the immunological significance of CD23-mediated antigen presentation?
CD23 participates in a specialized antigen presentation process known as IgE-facilitated antigen presentation. In this process, B cells capture IgE-allergen complexes through surface CD23 and subsequently present allergen peptides to T lymphocytes via MHC class II molecules. This mechanism plays a key role in the initiation and maintenance of allergic reactions. Successful allergen-specific immunotherapy can induce the production of protective IgG4 antibodies, which competitively inhibit IgE binding to CD23, thereby blocking allergen presentation and promoting immune tolerance.
5. How do interactions between CD23 and other immune molecules affect immune function?
The interaction between CD23 and complement receptor CD21 constitutes another important regulatory layer. Due to differences in binding sites, CD21 binding to CD23 does not interfere with IgE binding but may instead enhance CD23's affinity for IgE. Different IgG subclasses have differential effects on this interaction, with IgG4 potentially modulating B cell interactions with immune complexes by interfering with CD23-CD21 binding. These complex intermolecular networks reveal the multidimensional functions of CD23 in immune regulation.
6. What challenges and opportunities exist for CD23-targeted therapeutic strategies?
Although monoclonal antibodies targeting IgE have achieved significant success in treating allergic diseases, direct CD23-targeting strategies face more challenges. Research suggests that simply blocking CD23-IgE interactions may be insufficient to effectively alleviate allergic symptoms, likely due to CD23's complex dual functions in immune regulation. Future therapeutic development requires deeper understanding of CD23's specific roles under different physiological and pathological conditions, and exploration of more precise intervention strategies. Given CD23's multiple functions in IgE clearance, synthesis inhibition, and immune regulation, this target remains valuable for therapeutic development.
7. Conclusion
As a low-affinity receptor for IgE, CD23 participates in allergic response regulation through multiple mechanisms. From negative regulation of IgE synthesis to specialized antigen presentation functions, from interactions with other immune receptors to biological effects of soluble forms, CD23 plays a complex yet crucial role in the pathogenesis of allergic diseases. In-depth understanding of CD23's functions not only provides new perspectives for allergy mechanism research but also establishes theoretical foundations for developing more effective therapeutic strategies. With continued research, CD23-targeted therapies are expected to demonstrate unique value in the field of allergic diseases.
8. Which manufacturers provide CD23 antibodies?
Hangzhou Start Biotech Co., Ltd. has independently developed the "S-RMab® CD23 Recombinant Rabbit Monoclonal Antibody" (Product Name: S-RMab® CD23 Recombinant Rabbit mAb (SDT-028-67), a high-specificity, excellent-sensitivity, and superior-staining-consistency antibody for detecting B cell activation markers. This product was developed using the proprietary S-RMab® recombinant rabbit monoclonal antibody technology platform and has been rigorously validated across multiple technical platforms including immunohistochemistry (IHC). It holds significant application value in B cell lymphoma diagnosis, immune response research, and allergic disease mechanism exploration.

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Product Information
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S-RMab® CD23 Recombinant Rabbit mAb (SDT-028-67) |
Host : Rabbit |
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FITC Rat Anti-Mouse CD23 Antibody (S-R672) |
Host : Rat Conjugation : FITC |
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FITC Rat Anti-Mouse CD23 Antibody (S-R672) |
Host : Rat Conjugation : FITC |
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PE Rat Anti-Mouse CD23 Antibody (S-R672) |
Host : Rat Conjugation : PE |
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Alexa Fluor® 647 Rat Anti-Mouse CD23 Antibody (S-R672) |
Host : Rat Conjugation : Alexa Fluor® 647 |
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Alexa Fluor® 488 Rat Anti-Mouse CD23 Antibody (S-R672) |
Host : Rat Conjugation : Alexa Fluor® 488 |