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The Journal of Immunology, 2001, 167: 407-415.
Copyright © 2001 by The American Association of Immunologists

Impaired Mucosal Immunity in L-Selectin-Deficient Mice Orally Immunized with a Salmonella Vaccine Vector1

David W. Pascual2, Michelle D. White, Trina Larson and Nancy Walters

Veterinary Molecular Biology, Montana State University, Bozeman, MT 59717

Lymphocyte trafficking in the gastrointestinal tract is primarily mediated by interactions with the mucosal addressin cell adhesion molecule 1 and its lymphocyte ligand, {alpha}4{beta}7, and partly by L-selectin (L-Sel) interactions with peripheral node addressin coexpressed on some mucosal addressin cell adhesion molecule 1. We inquired whether intestinal responses in mice lacking L-Sel would be enhanced. L-Sel-deficient (L-Sel-/-) mice were orally immunized with either Salmonella vaccine vector or Salmonella vector-expressing colonization factor Ag I (CFA/I) from enterotoxigenic Escherichia coli. In L-Sel-/- mice, mucosal IgA anti-CFA/I fimbrial responses were greatly reduced, and systemic IgG2a anti-CFA/I fimbrial responses were 26-fold greater compared with C57BL/6 (L-Sel+/+) mice. L-Sel-/- Peyer’s patch (PP) CD4+ Th cells revealed IFN-{gamma}-dominated responses and an unprecedented absence of IL-4, whereas the expected mixed Th cell phenotype developed in L-Sel+/+ mice. PP CD4+ Th cell anti-Salmonella responses were nearly nonexistent in L-Sel-/- mice immunized with either Salmonella vaccine. Splenic CD4+ Th cell anti-Salmonella responses were reduced but did show cytokine production in Ag restimulation assays. Increased colonization of PP and spleen was noted only with the Salmonella vector in L-Sel-/- mice, resulting in increased splenomegaly, suggesting that the Salmonella-CFA/I vaccine was not as infectious or that the presence of the fimbriae improved clearance, possibly because of reduced neutrophil recruitment. However, sufficient anti-Salmonella immunity was induced, because Salmonella vector-immunized L-Sel-/- mice showed complete protection against wild-type Salmonella challenge, unlike L-Sel+/+ mice. This evidence shows that L-Sel is important for development of mucosal immunity, and absence of L-Sel is protective against salmonellosis.




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