Table 1 Tools currently used to deplete pDCs or to inhibit their IFN production

From: The role of plasmacytoid dendritic cells (pDCs) in immunity during viral infections and beyond

Mutant mice

Genetic background

Principle/Advantage

Penetrance1

tDCs impacted

Other cell types impacted

CX3CR1-hDTR [65]

C57BL/6

Depletion of precursors common to pDCs, tDCs and cDCs

>90%

YES

cDC2

CD11c-Cre; Tcf4-/fl (CKO) [66]

C57BL/6

Loss of Tcf4 exclusively in CD11c+ cells, defect in pDC and tDC development

>90%

YES

ND2

Tcf4-/- [66]

129SvEvTac

defect in pDC development

>90%

YES

tDCs, pDC-like cells, monocytes, macrophages, and subsets of B cells

IkarosL/L [67]

C57BL/6

Hypomorphic Ikaros mutation, defect in pDC development

95%

ND

B cells, T cells, neutrophils

Siglech-hDTR [68]

C57BL/6

Bacterial artificial chromosome-based transgenic mice expressing hDTR under the control of Siglech regulatory regions

90-95%

ND

Marginal Zone Macrophages (MZM), pDC precursors and other specialized macrophages (e.g. microglia)

Siglech-hDTR [69]

C57BL/6

KI mice expressing hDTR under the control of the Siglech promoter

95%

ND

ND

CLEC4C-hDTR/BDCA2-hDTR [70]

C57BL/6

Transgenic mice expressing hDTR under the control of human CLEC4C/BDCA2 regulatory regions

90-95%

NO

NO

Antigen +  (antibody clone)

Targeted host

Principle/Advantage

Penetrance

Are tDCs impacted?

Other cell types impacted?

Ly6C/Ly6G (RB6-8C5) [16, 71]

Mouse

Depletion of pDCs as they express high levels of Ly6C

95%

ND

Neutrophils, monocytes, eosinophils, macrophages and activated T cells

Bst2 (120G8 or 927 Ab clones) [65, 72]

Depletion of pDCs as they express high levels of Bst2

94%

YES

tDCs, activated monocytes and B cells

SiglecH (440c Ab clone) [73]

Inhibition of IFN production by pDCs

90%

ND

Macrophages and DC progenitors

BDCA2 (Litifilimab) [74]

Human and Macaques

Depletion of pDCs as they express BDCA2

Data not shown

ND

ND

ILT7 (VIB7734) [75]

Depletion of pDCs as they express ILT7

50% in human, 80% in macaque

NO

ND

  1. 1Percent of the pDC population that is depleted, or in the case of anti-SiglecH administration, percent of inhibition of pDC IFN production; 2ND not determined