Research demonstrates MS4a4B's dual role in immune modulation :
| Function | Mechanism | Experimental Evidence |
|---|---|---|
| Anti-apoptotic activity | Reduces caspase 3/8/9 activation via unknown signaling pathways | EL4 cell apoptosis ↓50% with MS4a4B overexpression |
| Proliferation regulation | Inhibits overgrowth of activated T cells | siRNA knockdown ↑T32 cell apoptosis by 35% |
| Therapeutic targeting | Anti-MS4a4B antibodies induce apoptosis in autoreactive T cells | EAE severity ↓60% in antibody-treated mice |
Knockdown effects: MS4a4B siRNA increased staurosporine-induced apoptosis in T32 cells (p < 0.01) .
Overexpression: EL4 cells with forced MS4a4B expression showed 40% reduction in TCR-stimulated apoptosis .
EAE model: Anti-MS4a4B antibody administration:
MS4a4B-targeting antibodies show promise for:
Autoimmune diseases: Multiple sclerosis (via EAE model validation)
Cancer immunotherapy: Potential to deplete pathogenic T cell subsets
Combination therapies: Synergy with anti-CD20 agents for broader immune modulation
No publications directly addressing "MSRB4" exist in the provided sources.
Suggested actions:
Verify gene nomenclature (MS4A4B vs. putative MSRB4)
Explore UniProt (ID: Q96JQ5) or IEDB databases for additional epitope data
Conduct BLAST alignment to resolve sequence discrepancies
The following FAQs address key aspects of MS4A4B antibody research (note: "MSRB4" may refer to MS4A4B, a member of the MS4A transmembrane protein family; no data for MSRB4 were found in provided sources). Questions are stratified by research depth and supported by experimental evidence from published studies.
How do anti-MS4A4B antibodies mechanistically impair pathogenic T cell responses?
Proposed mechanism:
Experimental validation: Compare transcriptomes of antibody-treated vs. control T cells using RNA-seq to identify downstream pathways.
How to address variability in MS4A4B antibody performance across assays?
Troubleshooting table:
How to reconcile conflicting reports on MS4A4B’s role in T cell survival?
What controls are critical for in vivo anti-MS4A4B studies?