Table 1.
Stereotyped BCRs in TCL1+ CLL in mice
CLL BCR setIdentical VH/VK BCRTC+TC+ CD40–/–≤2 mo B1 B cell origin
IgHIgL
VH geneaVk genebn = 155n = 18n = 20
VH12-1 (V261) Vk4-91 (kf4) 40 (25.8 %) 4 (22.2%) 
J558-64 (V332) Vk12-89 (fl12) 19 (12.3 %) 3 (16.6%) 
Q52-1 (V222) Vk9-96 (ce9) 14 (9.0 %) 1 (5.6%) 
J558-67 (V328) Vk1-117 (cr1) 10 (6.5 %) 1 (5.6%) 
VH11-2 (V235) Vk9-128 (br9) 4 (2.6 %) 1 (5.6%) nd 
CLL BCR setIdentical VH/VK BCRTC+TC+ CD40–/–≤2 mo B1 B cell origin
IgHIgL
VH geneaVk genebn = 155n = 18n = 20
VH12-1 (V261) Vk4-91 (kf4) 40 (25.8 %) 4 (22.2%) 
J558-64 (V332) Vk12-89 (fl12) 19 (12.3 %) 3 (16.6%) 
Q52-1 (V222) Vk9-96 (ce9) 14 (9.0 %) 1 (5.6%) 
J558-67 (V328) Vk1-117 (cr1) 10 (6.5 %) 1 (5.6%) 
VH11-2 (V235) Vk9-128 (br9) 4 (2.6 %) 1 (5.6%) nd 

Presence of CLL stereotyped BCRs in TCL1+(TC+) CLL samples expressing identical VH and VL combination, including CD40 deficiency, and CLL developed by IgM+ B1 B cell transfer from TC+ neonatal/young mice (≤2 mo old). n, total sample number. nd, not detected.

a

VH gene (see Table S1 and Vbase2 for parentheses).

b

Vk gene (Thiebe et al., 1999).

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