FIGURE 5
FROM:
Distal IgA immunity can be sustained by
E
7
+ B cells in L-selectin-/- mice following oral immunization
D W Pascual, C Riccardi and K Csencsits-Smith
BACK TO ARTICLEFigure 5.

Effector CT-B-specific B cells were mostly L-Sellow/
7
low in the iLP and NP at 42 days post-primary immunization. Cell-sorting experiments were conducted sorting (a, b) iLP and (c, d) NP lymphocytes for
7 vs.
7
high and
E expression and assessed by CT-B-specific (left panel) and total (right panel) (a, c) IgA and (b, d) IgG ELISPOT. No
7
high B cells were found in either L-Sel+/+ or L-Sel-/- NP; all the iLP
7
high B cells were
E
7
+, not
4
7
high, and the
7
low B cells were all L-Sellow/
7
low. The majority of the CT-B-specific iLP IgA AFCs were
7
low. For both L-Sel+/+ and L-Sel-/- mice, the L-Sellow/
7
low B-cell subset contained all of the NP IgA anti-CT-B activity, and for L-Sel-/- mice,
E
7
+ B cells contained the IgG anti-CT-B and the total IgG AFCs. Results depict the mean of three experiments
s.e.m., and statistical differences between
7
low and
E
7
+ B cells were determined: *P
0.002; **P
0.008; ***P<0.026; ****P<0.05. AFC, antibody-forming cell; CT, cholera toxin; ELISPOT, enzyme-linked immunosorbent spot; Ig, immunoglobulin; iLP, intestinal lamina propria; L-Sel, L-selectin; NALT, nasal-associated lymphoid tissue; NP, nasal passage.
