Topic Highlight
Copyright ©2014 Baishideng Publishing Group Inc.
World J Diabetes. Dec 15, 2014; 5(6): 739-746
Published online Dec 15, 2014. doi: 10.4239/wjd.v5.i6.739
Table 1 Evidence for immune regulatory and β-cell autonomous roles of B7-H4 in experimental/human diabetes
RoleModelSummary of findingsApplicationRef.
Autoimmune modulatorNOD mouseB7-H4 Ig inhibits development of, and reverses newly-onset autoimmune diabetesPrevents/[31,33]
reverses T1D
Allograft protectionNIT cell lineB7-H4 transfected NIT cells promote β-cell allograft survivalSuppresses islet graft rejection[44]
MouseAdenoviral-transduced B7-H4 donor islets enhanced islet allograft survival, and promotes donor-specific tolerance[43,46]
MouseB7-H4 transgenic islets improve islet allograft survivalPreserves β-cell mass in T1D/T2D[51]
Non-immune dependent UPR and cell survivalPancreatic carcinoma-derived cell linesB7-H4 knock-down increases cell apoptosis[56]
regulatorRenal carcinoma tissues and cancer cell linesHuman intracellular B7-H4 is identified as a cytoplasmic-nuclear shuttling protein that contains a NLS[57]
MouseB7-H4 modulates UPR in isolated pancreatic β-cellsUnpublished
Biomarkers of β-cell immunityMouseB7-H4 RSS0.2 mRNA splice form is correlated with different stages of T1DDetects β-cell autoimmunityUnpublished
HumanReduced B7-H4 expression and B7-H4/insulin colocalization is detected in pancreata of T1D patients[25]
HumanElevated sB7-H4 is present in RA and newly-onset T1D patients[61,62]