• The B2M encodes a serum protein found in association with the major histocompatibility complex (MHC) class I heavy chain on the surface of nearly all nucleated cells. The protein has a predominantly beta-pleated sheet structure that can form amyloid fibrils in some pathological conditions. HLA-A belongs to the HLA class I heavy chain paralogues. The heavy chain is anchored in the membrane. Class I molecules play a central role in the immune system by presenting peptides derived from the endoplasmic reticulum lumen so that they can be recognized by cytotoxic T cells. They are expressed in nearly all cells.
• The B2M gene (Exon1 to Exon3) of mouse were replaced by the sequence encompassing the human B2M CDS and HLA-A*31:01 gene that included leader sequence, α1 and α2 domains ligated to a fragment of the murine H-2D^b gene containing the α3, transmembrane and cytoplasmic domains.
• Human B2M and HLA-A31.1 were exclusively detectable in homozygous B-HLA-A31.1 mice.
• B-HLA-A31.1 mice provide a powerful preclinical model for in vivo evaluation of vaccines.
• Application: For example, this product is used for pharmacodynamics and safety evaluation of vaccines for cancers.

Gene targeting strategy for B-HLA-A31.1 mice. The B2M gene (Exon1 to Exon3) of mouse were replaced by the sequence encompassing the human B2M CDS and HLA-A*31:01 gene that included leader sequence, α1 and α2 domains ligated to a fragment of the murine H-2D^b gene containing the α3, transmembrane and cytoplasmic domains.

Strain specific B2M expression analysis in wild-type C57BL/6JNifdc mice and homozygous humanized B-HLA-A31.1 mice by flow cytometry. Splenocytes(A) and blood(B) were collected from wild-type C57BL/6JNifdc mice (+/+) and homozygous B-HLA-A31.1 mice (H/H), respectively, and analyzed by flow cytometry with species-specific anti-hB2M (Biolegend, 395712), and anti-mB2M (BD Biosciences, 744802) antibody. Human B2M were exclusively detectable in homozygous B-HLA-A31.1 mice.

Strain specific HLA-A31.1 expression analysis in wild-type C57BL/6JNifdc mice and homozygous humanized B-HLA-A31.1 mice by flow cytometry. Splenocytes(A) and blood(B) were collected from wild-type C57BL/6JNifdc mice (+/+) and homozygous B-HLA-A31.1 mice (H/H), respectively, and analyzed by flow cytometry with species-specific anti-HLA-ABC (Biolegend, 311406) and anti-H-2Db (Biolegend, 111513). HLA-A31.1 were exclusively detectable in homozygous B-HLA-A31.1 mice.