Brugia pahangi:Differential Induction and Regulation of Jird Inflammatory Responses by Life-Cycle Stages
It has been hypothesized that different life-cycle stages of filarial nematodes induce different host responses. This concept was examined in theBrugia pahangi–jird model of lymphatic filariasis by measuring the kinetics of inflammatory responses to parasite antigens following intraperitoneal inocul...
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Veröffentlicht in: | Experimental parasitology 1997-09, Vol.87 (1), p.20-29 |
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description | It has been hypothesized that different life-cycle stages of filarial nematodes induce different host responses. This concept was examined in theBrugia pahangi–jird model of lymphatic filariasis by measuring the kinetics of inflammatory responses to parasite antigens following intraperitoneal inoculation of different life-cycle stages. For this purpose, viable female or male worms, L3, L4, or microfilarial stages, were used. Dead worms served as controls. Worm and microfilarial burdens, pulmonary granulomatous inflammation (PGRN) to soluble adult worm antigen (SAWA)-coated beads, and peritoneal eosinophil and macrophage numbers were assessed at different days post-inoculation. All jirds inoculated with any of these life-cycle stages developed an early PGRN to SAWA which was later significantly reduced. Only viable worms induced down-regulation of the PGRN response. These results indicate that the hyporesponsive state is induced and maintained by all life-cycle stages. Also, the degree of granulomatous response was influenced by worm burden, with larger worm burdens inducing lower initial levels of PGRN to SAWA. Peritoneal inflammatory responses differed from the systemic response in that numbers of macrophages increased with time and microfilarial accumulation. No correlation was observed between peritoneal inflammatory responses measured by eosinophil and macrophage numbers and PGRN to SAWA. |
doi_str_mv | 10.1006/expr.1997.4179 |
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This concept was examined in theBrugia pahangi–jird model of lymphatic filariasis by measuring the kinetics of inflammatory responses to parasite antigens following intraperitoneal inoculation of different life-cycle stages. For this purpose, viable female or male worms, L3, L4, or microfilarial stages, were used. Dead worms served as controls. Worm and microfilarial burdens, pulmonary granulomatous inflammation (PGRN) to soluble adult worm antigen (SAWA)-coated beads, and peritoneal eosinophil and macrophage numbers were assessed at different days post-inoculation. All jirds inoculated with any of these life-cycle stages developed an early PGRN to SAWA which was later significantly reduced. Only viable worms induced down-regulation of the PGRN response. These results indicate that the hyporesponsive state is induced and maintained by all life-cycle stages. Also, the degree of granulomatous response was influenced by worm burden, with larger worm burdens inducing lower initial levels of PGRN to SAWA. Peritoneal inflammatory responses differed from the systemic response in that numbers of macrophages increased with time and microfilarial accumulation. No correlation was observed between peritoneal inflammatory responses measured by eosinophil and macrophage numbers and PGRN to SAWA.</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1006/expr.1997.4179</identifier><identifier>PMID: 9287954</identifier><identifier>CODEN: EXPAAA</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Brugia ; BRUGIA PAHANGI ; Brugia pahangi - physiology ; Disease Models, Animal ; Down-Regulation ; Eosinophils - pathology ; Female ; Filariasis - parasitology ; Filariasis - pathology ; GERBILLE ; Gerbillinae ; GERBILS ; GERBO ; Granuloma - parasitology ; Granuloma - pathology ; granulomatous inflammation ; Helminthic diseases ; HOST PARASITE RELATIONS ; Host-Parasite Interactions ; IMMUNE RESPONSE ; immunoregulation ; Infectious diseases ; Inflammation - parasitology ; Inflammation - pathology ; Kinetics ; LARVAE ; LARVAS ; LARVE ; Lung Diseases - parasitology ; Lung Diseases - pathology ; lymphatic filariasis ; Macrophages, Peritoneal - pathology ; Male ; Medical sciences ; MERIONES UNGUICULATUS ; MICROFILARIAE ; Microspheres ; Miscellaneous ; NEMATODA ; nematode ; Parasitic diseases ; Peritoneal Cavity - pathology ; RELACIONES HUESPED PARASITO ; RELATION HOTE PARASITE ; REPONSE IMMUNITAIRE ; RESPUESTA INMUNOLOGICA</subject><ispartof>Experimental parasitology, 1997-09, Vol.87 (1), p.20-29</ispartof><rights>1997 Academic Press</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-cd24cf9136eecbca7a0f4aa1f5c2f8935ba4043fd3b5aed294dc78b70ecf24a03</citedby><cites>FETCH-LOGICAL-c387t-cd24cf9136eecbca7a0f4aa1f5c2f8935ba4043fd3b5aed294dc78b70ecf24a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/expr.1997.4179$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2815101$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9287954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nasarre, C.</creatorcontrib><creatorcontrib>Coleman, S.U.</creatorcontrib><creatorcontrib>Rao, U.R.</creatorcontrib><creatorcontrib>Klei, T.R.</creatorcontrib><title>Brugia pahangi:Differential Induction and Regulation of Jird Inflammatory Responses by Life-Cycle Stages</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>It has been hypothesized that different life-cycle stages of filarial nematodes induce different host responses. This concept was examined in theBrugia pahangi–jird model of lymphatic filariasis by measuring the kinetics of inflammatory responses to parasite antigens following intraperitoneal inoculation of different life-cycle stages. For this purpose, viable female or male worms, L3, L4, or microfilarial stages, were used. Dead worms served as controls. Worm and microfilarial burdens, pulmonary granulomatous inflammation (PGRN) to soluble adult worm antigen (SAWA)-coated beads, and peritoneal eosinophil and macrophage numbers were assessed at different days post-inoculation. All jirds inoculated with any of these life-cycle stages developed an early PGRN to SAWA which was later significantly reduced. Only viable worms induced down-regulation of the PGRN response. These results indicate that the hyporesponsive state is induced and maintained by all life-cycle stages. Also, the degree of granulomatous response was influenced by worm burden, with larger worm burdens inducing lower initial levels of PGRN to SAWA. Peritoneal inflammatory responses differed from the systemic response in that numbers of macrophages increased with time and microfilarial accumulation. No correlation was observed between peritoneal inflammatory responses measured by eosinophil and macrophage numbers and PGRN to SAWA.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brugia</subject><subject>BRUGIA PAHANGI</subject><subject>Brugia pahangi - physiology</subject><subject>Disease Models, Animal</subject><subject>Down-Regulation</subject><subject>Eosinophils - pathology</subject><subject>Female</subject><subject>Filariasis - parasitology</subject><subject>Filariasis - pathology</subject><subject>GERBILLE</subject><subject>Gerbillinae</subject><subject>GERBILS</subject><subject>GERBO</subject><subject>Granuloma - parasitology</subject><subject>Granuloma - pathology</subject><subject>granulomatous inflammation</subject><subject>Helminthic diseases</subject><subject>HOST PARASITE RELATIONS</subject><subject>Host-Parasite Interactions</subject><subject>IMMUNE RESPONSE</subject><subject>immunoregulation</subject><subject>Infectious diseases</subject><subject>Inflammation - parasitology</subject><subject>Inflammation - pathology</subject><subject>Kinetics</subject><subject>LARVAE</subject><subject>LARVAS</subject><subject>LARVE</subject><subject>Lung Diseases - parasitology</subject><subject>Lung Diseases - pathology</subject><subject>lymphatic filariasis</subject><subject>Macrophages, Peritoneal - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>MERIONES UNGUICULATUS</subject><subject>MICROFILARIAE</subject><subject>Microspheres</subject><subject>Miscellaneous</subject><subject>NEMATODA</subject><subject>nematode</subject><subject>Parasitic diseases</subject><subject>Peritoneal Cavity - pathology</subject><subject>RELACIONES HUESPED PARASITO</subject><subject>RELATION HOTE PARASITE</subject><subject>REPONSE IMMUNITAIRE</subject><subject>RESPUESTA INMUNOLOGICA</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1v1DAQhi0EKtvClQMSUg6otyy246xjbrB8Fa2EROnZmtjj1Cixg50g9t-TsKveOI2s9_E7o4eQF4xuGaW7N_hnTFumlNwKJtUjsmFU0ZILoR6TDaVMlKJR4im5zPknpbRhXFyQC8UbqWqxIffv09x5KEa4h9D5tx-8c5gwTB764ibY2Uw-hgKCLb5jN_fw7xld8dUnuwCuh2GAKabjkucxhoy5aI_FwTss90fTY3E7QYf5GXnioM_4_DyvyN2njz_2X8rDt883-3eH0lSNnEpjuTBOsWqHaFoDEqgTAMzVhrtGVXULgorK2aqtAS1XwhrZtJKicVwAra7I9al3TPHXjHnSg88G-x4CxjlrqfhO0h1bwO0JNCnmnNDpMfkB0lEzqle1elWrV7V6Vbt8eHVuntsB7QN-drnkr885ZAO9SxCMzw8Yb1jN6Lr35QlzEDV0aUHubpUUoqrWjuYU4qLot8eks_EYDFqf0EzaRv-_8_4CH-6faw</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>Nasarre, C.</creator><creator>Coleman, S.U.</creator><creator>Rao, U.R.</creator><creator>Klei, T.R.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><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>19970901</creationdate><title>Brugia pahangi:Differential Induction and Regulation of Jird Inflammatory Responses by Life-Cycle Stages</title><author>Nasarre, C. ; Coleman, S.U. ; Rao, U.R. ; Klei, T.R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-cd24cf9136eecbca7a0f4aa1f5c2f8935ba4043fd3b5aed294dc78b70ecf24a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brugia</topic><topic>BRUGIA PAHANGI</topic><topic>Brugia pahangi - physiology</topic><topic>Disease Models, Animal</topic><topic>Down-Regulation</topic><topic>Eosinophils - pathology</topic><topic>Female</topic><topic>Filariasis - parasitology</topic><topic>Filariasis - pathology</topic><topic>GERBILLE</topic><topic>Gerbillinae</topic><topic>GERBILS</topic><topic>GERBO</topic><topic>Granuloma - parasitology</topic><topic>Granuloma - pathology</topic><topic>granulomatous inflammation</topic><topic>Helminthic diseases</topic><topic>HOST PARASITE RELATIONS</topic><topic>Host-Parasite Interactions</topic><topic>IMMUNE RESPONSE</topic><topic>immunoregulation</topic><topic>Infectious diseases</topic><topic>Inflammation - parasitology</topic><topic>Inflammation - pathology</topic><topic>Kinetics</topic><topic>LARVAE</topic><topic>LARVAS</topic><topic>LARVE</topic><topic>Lung Diseases - parasitology</topic><topic>Lung Diseases - pathology</topic><topic>lymphatic filariasis</topic><topic>Macrophages, Peritoneal - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>MERIONES UNGUICULATUS</topic><topic>MICROFILARIAE</topic><topic>Microspheres</topic><topic>Miscellaneous</topic><topic>NEMATODA</topic><topic>nematode</topic><topic>Parasitic diseases</topic><topic>Peritoneal Cavity - pathology</topic><topic>RELACIONES HUESPED PARASITO</topic><topic>RELATION HOTE PARASITE</topic><topic>REPONSE IMMUNITAIRE</topic><topic>RESPUESTA INMUNOLOGICA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nasarre, C.</creatorcontrib><creatorcontrib>Coleman, S.U.</creatorcontrib><creatorcontrib>Rao, U.R.</creatorcontrib><creatorcontrib>Klei, T.R.</creatorcontrib><collection>AGRIS</collection><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>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nasarre, C.</au><au>Coleman, S.U.</au><au>Rao, U.R.</au><au>Klei, T.R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brugia pahangi:Differential Induction and Regulation of Jird Inflammatory Responses by Life-Cycle Stages</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>87</volume><issue>1</issue><spage>20</spage><epage>29</epage><pages>20-29</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><coden>EXPAAA</coden><abstract>It has been hypothesized that different life-cycle stages of filarial nematodes induce different host responses. This concept was examined in theBrugia pahangi–jird model of lymphatic filariasis by measuring the kinetics of inflammatory responses to parasite antigens following intraperitoneal inoculation of different life-cycle stages. For this purpose, viable female or male worms, L3, L4, or microfilarial stages, were used. Dead worms served as controls. Worm and microfilarial burdens, pulmonary granulomatous inflammation (PGRN) to soluble adult worm antigen (SAWA)-coated beads, and peritoneal eosinophil and macrophage numbers were assessed at different days post-inoculation. All jirds inoculated with any of these life-cycle stages developed an early PGRN to SAWA which was later significantly reduced. Only viable worms induced down-regulation of the PGRN response. These results indicate that the hyporesponsive state is induced and maintained by all life-cycle stages. Also, the degree of granulomatous response was influenced by worm burden, with larger worm burdens inducing lower initial levels of PGRN to SAWA. Peritoneal inflammatory responses differed from the systemic response in that numbers of macrophages increased with time and microfilarial accumulation. No correlation was observed between peritoneal inflammatory responses measured by eosinophil and macrophage numbers and PGRN to SAWA.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>9287954</pmid><doi>10.1006/expr.1997.4179</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Brugia BRUGIA PAHANGI Brugia pahangi - physiology Disease Models, Animal Down-Regulation Eosinophils - pathology Female Filariasis - parasitology Filariasis - pathology GERBILLE Gerbillinae GERBILS GERBO Granuloma - parasitology Granuloma - pathology granulomatous inflammation Helminthic diseases HOST PARASITE RELATIONS Host-Parasite Interactions IMMUNE RESPONSE immunoregulation Infectious diseases Inflammation - parasitology Inflammation - pathology Kinetics LARVAE LARVAS LARVE Lung Diseases - parasitology Lung Diseases - pathology lymphatic filariasis Macrophages, Peritoneal - pathology Male Medical sciences MERIONES UNGUICULATUS MICROFILARIAE Microspheres Miscellaneous NEMATODA nematode Parasitic diseases Peritoneal Cavity - pathology RELACIONES HUESPED PARASITO RELATION HOTE PARASITE REPONSE IMMUNITAIRE RESPUESTA INMUNOLOGICA |
title | Brugia pahangi:Differential Induction and Regulation of Jird Inflammatory Responses by Life-Cycle Stages |
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