Mucosal Immunology

FIGURE 5

FROM:

Distal IgA immunity can be sustained by alphaEbold beta7 + B cells in L-selectin-/- mice following oral immunization

D W Pascual, C Riccardi and K Csencsits-Smith

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Figure 5.

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Effector CT-B-specific B cells were mostly L-Sellow/beta7 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 beta7 vs. beta7 high and alphaE expression and assessed by CT-B-specific (left panel) and total (right panel) (a, c) IgA and (b, d) IgG ELISPOT. No beta7 high B cells were found in either L-Sel+/+ or L-Sel-/- NP; all the iLP beta7 high B cells were alphaEbeta7 +, not alpha4beta7 high, and the beta7 low B cells were all L-Sellow/beta7 low. The majority of the CT-B-specific iLP IgA AFCs were beta7 low. For both L-Sel+/+ and L-Sel-/- mice, the L-Sellow/beta7 low B-cell subset contained all of the NP IgA anti-CT-B activity, and for L-Sel-/- mice, alphaEbeta7 + B cells contained the IgG anti-CT-B and the total IgG AFCs. Results depict the mean of three experiments plusminuss.e.m., and statistical differences between beta7 low and alphaEbeta7 + B cells were determined: *Pless than or equal to0.002; **Pless than or equal to0.008; ***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.

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