Induction of oral tolerance to cellular immune responses in the absence of Peyer's patches
Open Access
- 29 March 2001
- journal article
- research article
- Published by Wiley in European Journal of Immunology
- Vol. 31 (4) , 1278-1287
- https://doi.org/10.1002/1521-4141(200104)31:4<1278::aid-immu1278>3.0.co;2-a
Abstract
Systemic hyporesponsiveness occurs following oral administration of antigen (oral tolerance) and involves the uptake and processing of antigen by the gut‐associated lymphoid tissue (GALT), which includes Peyer's patches (PP) lamina propria lymphocytes and mesenteric lymph nodes (MLN). Animals with targeted mutations of genes in the tumor necrosis factor (TNF) family have differential defects in the development of peripheral lymphoid organs including PP and MLN, and provide a unique opportunity to investigate the role of GALT structures in the induction of oral tolerance. Oral tolerance could not be induced in TNF/lymphotoxin (LT) α–/– mice, which are devoid of both PP and MLN, although these animals could be tolerized by intraperitoneal administration of antigen, demonstrating the requirement for GALT for oral tolerance induction. LTβ–/– mice and LTα/LTβ+/– animals do not have PP but could be orally tolerized, as measured by IFN‐γ production and delayed‐type hypersensitivity responses by administration of both low or high doses of ovalbumin. To further investigate the requirement for PP, we tested the progeny of LTβ‐receptor‐IgG‐fusion‐protein (LTβRigG)‐treated mice, which do not form PP but have an otherwise intact immune system. Although these animals had decreased fecal IgA production, they could be orally tolerized. Our results demonstrate that PP are not an absolute requirement for the induction of either high‐ or low‐dose oral tolerance, although oral tolerance could not be induced in animals devoid of both PP and MLN.Keywords
This publication has 43 references indexed in Scilit:
- The Spleen and Organized Lymph Nodes Are Not Essential for the Development of Gut-Induced Mucosal Immune Responses in Lymphotoxin-α Deficient MiceClinical Immunology and Immunopathology, 1998
- Complementation of Lymphotoxin α Knockout Mice with Tumor Necrosis Factor–expressing Transgenes Rectifies Defective Splenic Structure and FunctionThe Journal of Experimental Medicine, 1998
- A Role for Tumor Necrosis Factor Receptor Type 1 in Gut-associated Lymphoid Tissue Development: Genetic Evidence of Synergism with Lymphotoxin βThe Journal of Experimental Medicine, 1998
- Selective disruption of lymphotoxin ligands reveals a novel set of mucosal lymph nodes and unique effects on lymph node cellular organizationInternational Immunology, 1997
- Oral Tolerance to Myelin Basic Protein Induces Regulatory TGF-β-Secreting T Cells in Peyer's Patches of SJL MiceCellular Immunology, 1994
- Published by American Association for the Advancement of Science (AAAS) ,1994
- A Lymphotoxin-β-Specific ReceptorScience, 1994
- Abnormal Development of Peripheral Lymphoid Organs in Mice Deficient in LymphotoxinScience, 1994
- CD1d is involved in T cell-intestinal epithelial cell interactions.The Journal of Experimental Medicine, 1993
- Evidence for function of Ia molecules on gut epithelial cells in man.The Journal of Experimental Medicine, 1987