Induction of systemic immunologic tolerance to β-lactoglobulin by oral administration of a whey protein hydrolysate

Background: Oral administration of an antigen has been shown to suppress the specific immune response to this antigen. This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases. Objective: The purpose of this s...

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Veröffentlicht in:Journal of allergy and clinical immunology 1997-08, Vol.100 (2), p.266-273
Hauptverfasser: Fritsché, Rodolphe, Pahud, Jean Jacques, Pecquet, Sophie, Pfeifer, Andrea
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container_issue 2
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container_title Journal of allergy and clinical immunology
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creator Fritsché, Rodolphe
Pahud, Jean Jacques
Pecquet, Sophie
Pfeifer, Andrea
description Background: Oral administration of an antigen has been shown to suppress the specific immune response to this antigen. This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases. Objective: The purpose of this study was to determine whether oral tolerance can be induced with protein peptides. Partially hydrolyzed and extensively hydrolyzed cow's milk formulas were compared for their capacity to induce tolerance to cow's milk proteins. Methods: Five-week-old Sprague-Dawley rats were fed cow's milk formulas ad libitum from day 1 to day 19. All animals were immunized with β-lactoglobulin and ovalbumin on day 5 and bled on day 19. Sera were analyzed for specific IgE and IgG antibodies by ELISA and for functional IgE response by in vitro mast cell mediator (tritiated serotonin) release. In vivo modulation of intestinal mast cells was analyzed by the specific release of the rat mast cell protease II, and T-cell response was determined by tritiated thymidine incorporation into lymph node lymphocytes. Results: Oral administration of a partially hydrolyzed cow's milk formula suppresses specific serum IgE and IgG anti-β-lactoglobulin antibodies, as well as mediator release from rat mast cells and T-lymphocyte response. This suppression was shown to be antigen-specific and dose-dependent. An extensively hydrolyzed formula was unable to achieve the induction of such an oral tolerance. Conclusion: These results support the view that partially hydrolyzed proteins are able to induce specific oral tolerance, whereas extensively hydrolyzed proteins are not. (J Allergy Clin Immunol 1997;100:266-73.)
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This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases. Objective: The purpose of this study was to determine whether oral tolerance can be induced with protein peptides. Partially hydrolyzed and extensively hydrolyzed cow's milk formulas were compared for their capacity to induce tolerance to cow's milk proteins. Methods: Five-week-old Sprague-Dawley rats were fed cow's milk formulas ad libitum from day 1 to day 19. All animals were immunized with β-lactoglobulin and ovalbumin on day 5 and bled on day 19. Sera were analyzed for specific IgE and IgG antibodies by ELISA and for functional IgE response by in vitro mast cell mediator (tritiated serotonin) release. In vivo modulation of intestinal mast cells was analyzed by the specific release of the rat mast cell protease II, and T-cell response was determined by tritiated thymidine incorporation into lymph node lymphocytes. Results: Oral administration of a partially hydrolyzed cow's milk formula suppresses specific serum IgE and IgG anti-β-lactoglobulin antibodies, as well as mediator release from rat mast cells and T-lymphocyte response. This suppression was shown to be antigen-specific and dose-dependent. An extensively hydrolyzed formula was unable to achieve the induction of such an oral tolerance. Conclusion: These results support the view that partially hydrolyzed proteins are able to induce specific oral tolerance, whereas extensively hydrolyzed proteins are not. 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This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases. Objective: The purpose of this study was to determine whether oral tolerance can be induced with protein peptides. Partially hydrolyzed and extensively hydrolyzed cow's milk formulas were compared for their capacity to induce tolerance to cow's milk proteins. Methods: Five-week-old Sprague-Dawley rats were fed cow's milk formulas ad libitum from day 1 to day 19. All animals were immunized with β-lactoglobulin and ovalbumin on day 5 and bled on day 19. Sera were analyzed for specific IgE and IgG antibodies by ELISA and for functional IgE response by in vitro mast cell mediator (tritiated serotonin) release. In vivo modulation of intestinal mast cells was analyzed by the specific release of the rat mast cell protease II, and T-cell response was determined by tritiated thymidine incorporation into lymph node lymphocytes. Results: Oral administration of a partially hydrolyzed cow's milk formula suppresses specific serum IgE and IgG anti-β-lactoglobulin antibodies, as well as mediator release from rat mast cells and T-lymphocyte response. This suppression was shown to be antigen-specific and dose-dependent. An extensively hydrolyzed formula was unable to achieve the induction of such an oral tolerance. Conclusion: These results support the view that partially hydrolyzed proteins are able to induce specific oral tolerance, whereas extensively hydrolyzed proteins are not. (J Allergy Clin Immunol 1997;100:266-73.)</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antibody Specificity</subject><subject>Biological and medical sciences</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Experimental and animal immunopathology. Animal models</subject><subject>hydrolysate</subject><subject>IgE</subject><subject>Immune Tolerance</subject><subject>Immunoglobulin E - blood</subject><subject>Immunopathology</subject><subject>Intestinal Mucosa - cytology</subject><subject>Lactoglobulins - immunology</subject><subject>Lymphocyte Activation - drug effects</subject><subject>Lymphocyte Activation - immunology</subject><subject>Male</subject><subject>mast cells</subject><subject>Mast Cells - metabolism</subject><subject>Medical sciences</subject><subject>Milk - chemistry</subject><subject>Milk Proteins - pharmacology</subject><subject>Oral tolerance</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>whey protein</subject><subject>Whey Proteins</subject><subject>β-lactoglobulin</subject><issn>0091-6749</issn><issn>1097-6825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMuOFCEUQInRjO3oJ0zCwhhdlPIooFgZM_ExySQu1DWh4NYMhipGoDT1W36I3yQ93fbWFZfcc18HoQtKXlNC5ZsvhGjaSdXrl1q9UoRx0YkHaEeJVp0cmHiIdifkMXpSynfS_nzQZ-hMMyWooDtUrxa_uhrSgtOEy1YqzMHhMM_rkmK6aXFNEbJdHLQI__ndRetquolpXGNY8LjhlG3E1s9hCaVm-6-Zxb9uYcN3OVVo4O3mc4pbsRWeokeTjQWeHd9z9O3D-6-Xn7rrzx-vLt9dd66XonZq7EmvneeaMU1tD5pJy0GydiFzbvTeSxB61JQOSnnOp9FNTjKuqei9ovwcvTj0bTv8WKFUM4fiIEa7QFqLUZrxYZCqgeIAupxKyTCZuxxmmzdDidnbNve2zV6l0crc2zai1V0cB6zjDP5UddTb8s-PeVucjdNeYygnjKlBaMob9vaAQZPxM0A2xQVoxn3I4KrxKfxnkb-6w57Z</recordid><startdate>19970801</startdate><enddate>19970801</enddate><creator>Fritsché, Rodolphe</creator><creator>Pahud, Jean Jacques</creator><creator>Pecquet, Sophie</creator><creator>Pfeifer, Andrea</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19970801</creationdate><title>Induction of systemic immunologic tolerance to β-lactoglobulin by oral administration of a whey protein hydrolysate</title><author>Fritsché, Rodolphe ; Pahud, Jean Jacques ; Pecquet, Sophie ; Pfeifer, Andrea</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c465t-7b4049cd392291a4e926a3e620972ccbddd6e59b911877d33fbcfc6239154d713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antibody Specificity</topic><topic>Biological and medical sciences</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Experimental and animal immunopathology. Animal models</topic><topic>hydrolysate</topic><topic>IgE</topic><topic>Immune Tolerance</topic><topic>Immunoglobulin E - blood</topic><topic>Immunopathology</topic><topic>Intestinal Mucosa - cytology</topic><topic>Lactoglobulins - immunology</topic><topic>Lymphocyte Activation - drug effects</topic><topic>Lymphocyte Activation - immunology</topic><topic>Male</topic><topic>mast cells</topic><topic>Mast Cells - metabolism</topic><topic>Medical sciences</topic><topic>Milk - chemistry</topic><topic>Milk Proteins - pharmacology</topic><topic>Oral tolerance</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>whey protein</topic><topic>Whey Proteins</topic><topic>β-lactoglobulin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fritsché, Rodolphe</creatorcontrib><creatorcontrib>Pahud, Jean Jacques</creatorcontrib><creatorcontrib>Pecquet, Sophie</creatorcontrib><creatorcontrib>Pfeifer, Andrea</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of allergy and clinical immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fritsché, Rodolphe</au><au>Pahud, Jean Jacques</au><au>Pecquet, Sophie</au><au>Pfeifer, Andrea</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of systemic immunologic tolerance to β-lactoglobulin by oral administration of a whey protein hydrolysate</atitle><jtitle>Journal of allergy and clinical immunology</jtitle><addtitle>J Allergy Clin Immunol</addtitle><date>1997-08-01</date><risdate>1997</risdate><volume>100</volume><issue>2</issue><spage>266</spage><epage>273</epage><pages>266-273</pages><issn>0091-6749</issn><eissn>1097-6825</eissn><coden>JACIBY</coden><abstract>Background: Oral administration of an antigen has been shown to suppress the specific immune response to this antigen. This approach, called oral tolerance, has been demonstrated with intact proteins in animal models for prevention of allergy and autoimmune diseases. Objective: The purpose of this study was to determine whether oral tolerance can be induced with protein peptides. Partially hydrolyzed and extensively hydrolyzed cow's milk formulas were compared for their capacity to induce tolerance to cow's milk proteins. Methods: Five-week-old Sprague-Dawley rats were fed cow's milk formulas ad libitum from day 1 to day 19. All animals were immunized with β-lactoglobulin and ovalbumin on day 5 and bled on day 19. Sera were analyzed for specific IgE and IgG antibodies by ELISA and for functional IgE response by in vitro mast cell mediator (tritiated serotonin) release. In vivo modulation of intestinal mast cells was analyzed by the specific release of the rat mast cell protease II, and T-cell response was determined by tritiated thymidine incorporation into lymph node lymphocytes. Results: Oral administration of a partially hydrolyzed cow's milk formula suppresses specific serum IgE and IgG anti-β-lactoglobulin antibodies, as well as mediator release from rat mast cells and T-lymphocyte response. This suppression was shown to be antigen-specific and dose-dependent. An extensively hydrolyzed formula was unable to achieve the induction of such an oral tolerance. Conclusion: These results support the view that partially hydrolyzed proteins are able to induce specific oral tolerance, whereas extensively hydrolyzed proteins are not. (J Allergy Clin Immunol 1997;100:266-73.)</abstract><cop>New York, NY</cop><pub>Mosby, Inc</pub><pmid>9275151</pmid><doi>10.1016/S0091-6749(97)70235-5</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Administration, Oral
Animals
Antibody Specificity
Biological and medical sciences
Enzyme-Linked Immunosorbent Assay
Experimental and animal immunopathology. Animal models
hydrolysate
IgE
Immune Tolerance
Immunoglobulin E - blood
Immunopathology
Intestinal Mucosa - cytology
Lactoglobulins - immunology
Lymphocyte Activation - drug effects
Lymphocyte Activation - immunology
Male
mast cells
Mast Cells - metabolism
Medical sciences
Milk - chemistry
Milk Proteins - pharmacology
Oral tolerance
Rats
Rats, Sprague-Dawley
whey protein
Whey Proteins
β-lactoglobulin
title Induction of systemic immunologic tolerance to β-lactoglobulin by oral administration of a whey protein hydrolysate
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