|Strain Name||C57BL/6-Btlatm1(hBTLA)/Bcgen||Common Name||B-hBTLA mice|
|Catalog number (Males)||BCM018M||Catalog number (Females)||BCM018F|
|Related Genes||Btla (B and T lymphoc yte associated)|
BTLA (B and T lymphocyte associated) is a B cell and T cell attenuator, another checkpoint negative regulator of the Ig superfamily. It is structurally similar to CTLA-4 and PD-1, and is expressed in B cells, T cells, NK cells, dendritic cells and macrophages. BTLA binds to its ligand HVEM (a member of the tumor necrosis factor receptor superfamily) to transmit a co-inhibition signal. BTLA plays a negative regulatory role in the body's anti-tumor immune response, and is associated with the immune escape mechanism of the tumor. BTLA inhibitors enhance the TCR signaling pathway and restore T cell function, and become potential novel targets for tumor biotherapy.
mRNA expression analysis
Fig 1. RT-PCR analysis of BTLA gene.
The hBTLA, but not mBTLA, mRNA was detected in splenocytes of the homozygous B-hBTLA mice.
Protein expression analysis
Fig 2. Splenocytes from both wild type (WT) C57BL/6 and the B-hBTLA homozygous mice were analyzed by flow cytometry.
Mouse BTLA+ B cells were detected in the WT mice, while human BTLA+ B cells were detected in the homozygous B-hBTLA mice.
BTLA Abs efficacy evaluation
Fig 3. Murine colon cancer MC38-hHVEM cells were subcutaneously implanted into homozygous B-hBTLA mice. Mice were grouped when the tumor size was approximately 150±50mm3 (n=6). Two human BTLA antibodies inhibited tumor growth differently, confirming that the B-hBTLA mouse model is a powerful tool for in vivo BTLA antibody pharmacological efficacy studies. (A) Tumor average volume ± SEM, (B) Mice average weight ± SEM.