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. Author manuscript; available in PMC: 2014 Jun 23.
Published in final edited form as: Circ Res. 2014 May 23;114(11):1743–1756. doi: 10.1161/CIRCRESAHA.113.301145

Table 2. Summary of Experimental Studies With Respect to the Role of Different B-Cell Subsets in Atherosclerosis.

Atherosclerosis Studies in Mice That Involve Different B-Cell Subsets Effect on Atherosclerosis B-Cell Subsets (Potentially) Affected
B1a B1b IRA MZ FO Bregs
Adoptive CD19+ B-cell transfer (20×106) into splenectomized or shamoperated Apoe−/− mice22
Reconstitution of Ldlr−/− mice with B-cell–deficient (μMT) bone marrow23
CD20 antibody treatment of Apoe−/− and Ldlr−/− mice24,25 (✓) ?
Adoptive transfer of splenic CD43− B cells into lymphocyte-deficient Rag2−/−γ-chain−/−Apoe−/− (5×106 or 5×107) or B-cell–deficient μMT/Apoe−/− (5×106) mice25
Adoptive transfer of splenic CD43− B cells (3×107 or 6×107) into B-cell–deficient μMT/Apoe−/− mice28
Adoptive transfer of wild-type but not sIgM−/− B1a cells (105 every 3 wk) into splenectomized atherosclerotic Apoe−/− mice29
BAFFR-deficient Apoe−/− or Ldlr−/− mice24,30 (✓) ?
Anti-BAFFR treatment of Apoe−/− mice31 (✓) ?
Reconstitution of Ldlr−/− mice with 50% GM-CSF and 50% B-cell–deficient (μMT) bone marrow to achieve GM-CSF deficiency in B cells only32

Apoe−/− indicates apolipoprotein E deficient; BAFFR, B-cell–activating factor receptor; Bregs, regulatory B cells; FO, follicular; IRA, innate response activator; Ldlr−/−, low-density lipoprotein receptor; and MZ, marginal zone.