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. 2012 Dec 1;1(9):1623–1625. doi: 10.4161/onci.21650

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Figure 1. Three proposed roles for CD20+ tumor-infiltrating lymphocytes (TILs) in promoting anti-tumor immunity. (A) CD20+ TILs as antigen presenting cells. B cells can bind tumor antigens via surface Ig molecules, process them and then present peptides to CD8+ and CD4+ T cells via MHC Class I and Class II, respectively. (B) CD20+ TILs as lymphoid organizers. B cells are able to secrete lymphotoxin, which can induce stromal cells to express adhesion molecules, cytokines and chemokines. These factors, in turn, can recruit and retain other lymphocytes. (C) CD20+ TILs as polarizing cells. Type-I and Type-II B effector cells (Be1 and Be2) can secrete cytokines such as interferon γ (IFNγ) and interleukin-4 (IL-4), which can skew T-cell responses toward Th1, Th2 or other functional states.