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LPS and inactivated Propionibacterium acnes elicit a partially protective response in primary infections of Heligmosomoides polygyrus
Intestinal helminth infections are common and of paramount economic importance in domestic animals. Available chemotherapy is limited and anthelmintic resistance is widespread in some hosts. This scenario favors the exploration of alternative methods of control, among them immune modulators. The eff...
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Published in: | Veterinary parasitology 2014-06, Vol.203 (1-2), p.231-236 |
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creator | González-Sánchez, Elena Corral, María-Jesús Mohamed Fawzi, Elshaima Rodríguez-Bertos, Antonio Alunda, José Mª Cuquerella, Montserrat |
description | Intestinal helminth infections are common and of paramount economic importance in domestic animals. Available chemotherapy is limited and anthelmintic resistance is widespread in some hosts. This scenario favors the exploration of alternative methods of control, among them immune modulators. The effect of Escherichia coli LPS+Propionibacterium acnes on a primary infection of Heligmosomoides polygyrus (Trichostongyloidea) in mice has been tested. Nematode infection induced a rise of specific IgG1, both serum and intestinal, and a significant reduction in the unspecific (ConA) lymphoproliferative response. Treatment with the immune modulator (days −2, 0, 7 and 14 post infection) elicited an apparent delay of larval intramucosal development. Moreover cumulative nematode egg shedding in treated mice was significantly lower (p=0.0041). Preliminary results point toward the interest of immune modulators to control intestinal helminths. |
doi_str_mv | 10.1016/j.vetpar.2014.02.026 |
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Available chemotherapy is limited and anthelmintic resistance is widespread in some hosts. This scenario favors the exploration of alternative methods of control, among them immune modulators. The effect of Escherichia coli LPS+Propionibacterium acnes on a primary infection of Heligmosomoides polygyrus (Trichostongyloidea) in mice has been tested. Nematode infection induced a rise of specific IgG1, both serum and intestinal, and a significant reduction in the unspecific (ConA) lymphoproliferative response. Treatment with the immune modulator (days −2, 0, 7 and 14 post infection) elicited an apparent delay of larval intramucosal development. Moreover cumulative nematode egg shedding in treated mice was significantly lower (p=0.0041). Preliminary results point toward the interest of immune modulators to control intestinal helminths.</description><identifier>ISSN: 0304-4017</identifier><identifier>EISSN: 1873-2550</identifier><identifier>DOI: 10.1016/j.vetpar.2014.02.026</identifier><identifier>PMID: 24636785</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antibodies, Helminth - analysis ; Antibodies, Helminth - blood ; Antibody ; Antibody Formation - drug effects ; Antibody Formation - immunology ; Escherichia coli ; Feces - parasitology ; Heligmosomatoidea - immunology ; Heligmosomoides ; Helminths ; Immunologic Factors - pharmacology ; Immunomodulation - immunology ; Intestines - parasitology ; Intestines - pathology ; Larva ; Lipopolysaccharides - pharmacology ; LPS ; Lymphoproliferation ; Mice, Inbred BALB C ; Nematoda ; Parasite Egg Count ; Parasite Load ; Propionibacterium ; Propionibacterium acnes ; Propionibacterium acnes - immunology ; Strongylida Infections - immunology</subject><ispartof>Veterinary parasitology, 2014-06, Vol.203 (1-2), p.231-236</ispartof><rights>2014 Elsevier B.V.</rights><rights>Copyright © 2014 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-d34496a077d7dd42c2184bbed8059b8e179f1ff88dd07ee6c72bdb8867e8dbbc3</citedby><cites>FETCH-LOGICAL-c395t-d34496a077d7dd42c2184bbed8059b8e179f1ff88dd07ee6c72bdb8867e8dbbc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24636785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>González-Sánchez, Elena</creatorcontrib><creatorcontrib>Corral, María-Jesús</creatorcontrib><creatorcontrib>Mohamed Fawzi, Elshaima</creatorcontrib><creatorcontrib>Rodríguez-Bertos, Antonio</creatorcontrib><creatorcontrib>Alunda, José Mª</creatorcontrib><creatorcontrib>Cuquerella, Montserrat</creatorcontrib><title>LPS and inactivated Propionibacterium acnes elicit a partially protective response in primary infections of Heligmosomoides polygyrus</title><title>Veterinary parasitology</title><addtitle>Vet Parasitol</addtitle><description>Intestinal helminth infections are common and of paramount economic importance in domestic animals. Available chemotherapy is limited and anthelmintic resistance is widespread in some hosts. This scenario favors the exploration of alternative methods of control, among them immune modulators. The effect of Escherichia coli LPS+Propionibacterium acnes on a primary infection of Heligmosomoides polygyrus (Trichostongyloidea) in mice has been tested. Nematode infection induced a rise of specific IgG1, both serum and intestinal, and a significant reduction in the unspecific (ConA) lymphoproliferative response. Treatment with the immune modulator (days −2, 0, 7 and 14 post infection) elicited an apparent delay of larval intramucosal development. Moreover cumulative nematode egg shedding in treated mice was significantly lower (p=0.0041). Preliminary results point toward the interest of immune modulators to control intestinal helminths.</description><subject>Animals</subject><subject>Antibodies, Helminth - analysis</subject><subject>Antibodies, Helminth - blood</subject><subject>Antibody</subject><subject>Antibody Formation - drug effects</subject><subject>Antibody Formation - immunology</subject><subject>Escherichia coli</subject><subject>Feces - parasitology</subject><subject>Heligmosomatoidea - immunology</subject><subject>Heligmosomoides</subject><subject>Helminths</subject><subject>Immunologic Factors - pharmacology</subject><subject>Immunomodulation - immunology</subject><subject>Intestines - parasitology</subject><subject>Intestines - pathology</subject><subject>Larva</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>LPS</subject><subject>Lymphoproliferation</subject><subject>Mice, Inbred BALB C</subject><subject>Nematoda</subject><subject>Parasite Egg Count</subject><subject>Parasite Load</subject><subject>Propionibacterium</subject><subject>Propionibacterium acnes</subject><subject>Propionibacterium acnes - immunology</subject><subject>Strongylida Infections - immunology</subject><issn>0304-4017</issn><issn>1873-2550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNUdGK1DAUDaK44-ofiOTRl443aZqkL4Is6goDLqjPIU1ulwxtU5N2YD7A_zZlRh9FuJBwcu45N_cQ8prBngGT7477Ey6zTXsOTOyBl5JPyI5pVVe8aeAp2UENohLA1A15kfMRAARI9ZzccCFrqXSzI78OD9-onTwNk3VLONkFPX1IcQ5xCl2BMIV1pNZNmCkOwYWFWlpsl2CH4UznFBfcGpEmzHOcMhapAofRpnO59ttrgWns6X0ReBxjjmMMvujNcTg_ntOaX5JnvR0yvrqet-THp4_f7-6rw9fPX-4-HCpXt81S-VqIVlpQyivvBXecadF16DU0baeRqbZnfa-196AQpVO8853WUqH2XefqW_L2olvG_rliXswYssNhsBPGNRvWCOC1lI3-DyoXTLG2kYUqLlSXYs4Je3P9vmFgtqzM0VyyMltWBnipre3N1WHtRvR_m_6EUwjvLwQsKzkFTCa7gJNDH1LZqvEx_NvhN3F4q0o</recordid><startdate>20140616</startdate><enddate>20140616</enddate><creator>González-Sánchez, Elena</creator><creator>Corral, María-Jesús</creator><creator>Mohamed Fawzi, Elshaima</creator><creator>Rodríguez-Bertos, Antonio</creator><creator>Alunda, José Mª</creator><creator>Cuquerella, Montserrat</creator><general>Elsevier B.V</general><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><scope>7QL</scope><scope>C1K</scope></search><sort><creationdate>20140616</creationdate><title>LPS and inactivated Propionibacterium acnes elicit a partially protective response in primary infections of Heligmosomoides polygyrus</title><author>González-Sánchez, Elena ; 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subjects | Animals Antibodies, Helminth - analysis Antibodies, Helminth - blood Antibody Antibody Formation - drug effects Antibody Formation - immunology Escherichia coli Feces - parasitology Heligmosomatoidea - immunology Heligmosomoides Helminths Immunologic Factors - pharmacology Immunomodulation - immunology Intestines - parasitology Intestines - pathology Larva Lipopolysaccharides - pharmacology LPS Lymphoproliferation Mice, Inbred BALB C Nematoda Parasite Egg Count Parasite Load Propionibacterium Propionibacterium acnes Propionibacterium acnes - immunology Strongylida Infections - immunology |
title | LPS and inactivated Propionibacterium acnes elicit a partially protective response in primary infections of Heligmosomoides polygyrus |
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