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. Author manuscript; available in PMC: 2010 Feb 23.
Published in final edited form as: Eur J Immunol. 2000 Nov;30(11):3121–3131. doi: 10.1002/1521-4141(200011)30:11<3121::AID-IMMU3121>3.0.CO;2-M

Fig. 1.

Fig. 1

Expansion of Tg B cells in response to NP-Ficoll and NP-KLH. Recipients were challenged with either PBS (Naive), NP-Ficoll (TI Immune), or NP-KLH (TD Immune). (A) Spleen cells from naive and TI Immune recipients or lymph node cells from naive and TD Immune recipients were stained with NP-PE and B220 CyC on day 5 post-immunization. Kinetics of Tg B cell expansion from TI Immune (B) and TD Immune (C) recipients are shown on the indicated days. Mice that did not receive Tg B cells (no cells) were challenged with NP-Ficoll (B) or NP-KLH (C) and spleen or lymph node cells were used to control for the endogenous B cell response. Cell numbers are representative of three mice per group, and are normalized to the total number of spleen cells collected. Plots are representative of ten experiments.