Abbreviated name: BTLA
Synonyms: B- and T-lymphocyte attenuator | B- and T-lymphocyte-associated protein | CD272
Compound class:
Endogenous peptide in human, mouse or rat
Comment: BTLA is a negative immunomodulator. Interaction of BTLA with TNFRSF14 (HVEM) constitutes an immune checkpoint which inhibits T cell-mediated immune responses. Dysregulated BTLA expression contributes to immunosuppression and progression of some cancers [3-6] by enabling tumour immune evasion. Immunotherapeutics that block the BTLA-HVEM checkpoint offer potential as anti-tumour agents [7-8]. In the setting of inflammatory diseases anti-BTLA antibodies can induce inhibitory signalling and T cell activation, and reduce cytokine secretion [1].
There is information confirming two anti-BTLA monoclonals that were progressed to clinical development: HFB200603 (HiFiBiO; Phase 1 NCT05789069, solid tumours) [2] and ANB032 (AnaptysBio; Phase 2 NCT05935085, atopic dermatitis; terminated due to insufficient efficacy) [1].
Species: Human
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Selected 3D Structures | ||
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Post-translational Modification | |
Predicted N-linked glcosylation of asparagine residues at positions 45, 64 and 80; disulphide bond formation between cysteine residues at positions 4 and 33, 28 and 85, and 42 and 49 |