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. Author manuscript; available in PMC: 2018 Nov 1.
Published in final edited form as: Cell Immunol. 2017 Jul 19;321:8–17. doi: 10.1016/j.cellimm.2017.07.006

Table I.

Identification of CD11c+ and related B cells in mice and humans

Condition References Comments
Healthy humans [19] CD11c+ detected on activated B cells
Ehrlichial infection [1, 48] CD11c+ identified on spleen plasmablasts and IgM memory cells
Aged humans and SLE patients [35] [36] CD11c+ T-bet+ B cells (ABCs); autoreactive Abs detected in aged mice
Hairy Cell Leukemia (HCL) and variant [21, 91, 92] CD11c expression on IgM+ lymphoma cells; BRAF mutation is associated with cell growth
Viral infections [37] [38] CD11c+ T-bet+ B cells detected early in response to infections
Healthy humans [22] [23] CD11c expression detected on FcRL4+ non-germinal center memory B cells in tonsils
Healthy humans [24] CD11c expression detected on FcRL5 IgM+ CD21low tissue-like memory B cells
Healthy humans [93] CD11c+ expression on IgM+ memory cells in blood
Hepatitis C, B infection [33] [31], [94] [25] Accumulation of IgM+ CD11c+ CD21low memory B cells in patients with Mixed Cryoglobuliemia
HIV infection [29] IgM+ CD21low Tissue-like memory B cells increased in blood of viremic patients
Malaria infection [86] IgM+ memory B cells detected during infection
CVID [32, 95]; [30] IgM+ CD21low B cells with low SHM and poly- and auto-reactivity associated with splenomegaly
SLE [89] IgMlow CD21low B cells a present in the periphery of SLE patients