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
Hauptverfasser: Nasarre, C., Coleman, S.U., Rao, U.R., Klei, T.R.
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Coleman, S.U.
Rao, U.R.
Klei, T.R.
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. 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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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