Artificial lymph nodes induce potent secondary immune responses in naive and immunodeficient mice
J. Clin. Invest. Noriaki Okamoto, et al. 117:997 doi:10.1172/JCI30379 [
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Figure 4Increased number of IgG1 NP-specific AFCs in aLN-transplanted SCID mice after immunization with NP-OVA. (
A and
B) Number of NP-specific IgG AFCs in aLNs (
A) or spleens (
B) of aLN-transplanted SCID mice. Mice were immunized i.v. with NP-OVA on days 1 and 7 (100 μg/mouse and 10 μg/mouse, respectively) after transplantation of aLNs into SCID mice on day 0. The number of lymphocytes in spleens of aLN-transplanted SCID mice before and after NP-OVA immunization is denoted by the line (
B). (
C) Upon the second antigen stimulation, large numbers of IgG1 NP-specific AFCs were also detected in the BM of aLN-transplanted SCID mice. (
D) Number of NP-specific IgG AFCs in spleens of recipient SCID and BALB/c mice. (
E and
F) Number of NP-specific IgG AFCs in aLNs (
E) or spleens (
F) of aLN-transplanted SCID mice immunized i.v. with NP-OVA on days 7 and 14 (100 μg/mouse and 10 μg/mouse, respectively) after transplantation of aLNs into SCID mice on day 0. The number of lymphocytes in spleens of aLN-transplanted SCID mice before and after NP-OVA immunization is denoted by the line (
F).