IgG4 serology of loiasis in three villages in an endemic area of south‐eastern Gabon

Human filariasis due to Loa loa differs from other filariasis in that the majority of infected subjects are without circulating microfilariae (occult loiasis). In search for alternative diagnostic methods, which do not depend on circulating microfilariae or the (rather infrequent) eye‐passage of adu...

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Veröffentlicht in:Tropical medicine & international health 1998-04, Vol.3 (4), p.313-317
Hauptverfasser: Touré, Fousseyni S., Egwang, Thomas G., Millet, Pascal, Bain, Odile, Georges, Alain J., Wahl, Goetz
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container_end_page 317
container_issue 4
container_start_page 313
container_title Tropical medicine & international health
container_volume 3
creator Touré, Fousseyni S.
Egwang, Thomas G.
Millet, Pascal
Bain, Odile
Georges, Alain J.
Wahl, Goetz
description Human filariasis due to Loa loa differs from other filariasis in that the majority of infected subjects are without circulating microfilariae (occult loiasis). In search for alternative diagnostic methods, which do not depend on circulating microfilariae or the (rather infrequent) eye‐passage of adult worms, it was shown earlier that IgG4 antibodies directed against Loa loa adult worm antigen are apparently a good marker of occult loiasis and specific with regard to the sympatrically occurring Mansonella perstans. In this study we evaluated an IgG4 antibody‐based ELISA using crude extract of Loa loa microfilariae (which is easier to obtain than adult worm) to estimate the prevalence of loiasis in 3 villages in South‐East Gabon. Of 222 examined individuals (80 children < 16 years, 142 adults) 44 (20%) carried Loa loa microfilariae and 170 (77%) M. perstans. Using the mean OD‐value + 1 standard deviation of 9 sera from patients solely infected with M. perstans (from the Gambia, where Loa loa is not endemic) as a cut‐off, 35 of the 44 microfilaraemic Loa loa patients and 2 of the 9 Gambian controls were positive. This shows that our method had a sensitivity of 80% and a specificity of 78%. Among the remaining 178 subjects who had no microfilariae of Loa loa, as many as 97 (55%) had significant levels of specific IgG4 antibodies against Loa loa, suggesting that they carried occult loiasis. The mean IgG4 level in these putatively occult loiasis patients was slightly but significantly lower than in microfilaraemic subjects (P < 0.03). In conclusion, despite the limited sensitivity and specificity of our method, IgG4‐ ELISA at present is a very useful tool in estimating the real prevalence of loiasis in epidemiological surveys and at the individual level can confirm the diagnosis of L. loa amicrofilaraemic subjects with clinical signs suggesting loiasis.
doi_str_mv 10.1046/j.1365-3156.1998.00224.x
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This shows that our method had a sensitivity of 80% and a specificity of 78%. Among the remaining 178 subjects who had no microfilariae of Loa loa, as many as 97 (55%) had significant levels of specific IgG4 antibodies against Loa loa, suggesting that they carried occult loiasis. The mean IgG4 level in these putatively occult loiasis patients was slightly but significantly lower than in microfilaraemic subjects (P &lt; 0.03). In conclusion, despite the limited sensitivity and specificity of our method, IgG4‐ ELISA at present is a very useful tool in estimating the real prevalence of loiasis in epidemiological surveys and at the individual level can confirm the diagnosis of L. loa amicrofilaraemic subjects with clinical signs suggesting loiasis.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Animals</subject><subject>Antibodies, Helminth - blood</subject><subject>Antibody Formation</subject><subject>Antigens, Helminth - immunology</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Diseases caused by nematodes</subject><subject>endemic villages</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Filariases</subject><subject>Gabon - epidemiology</subject><subject>Helminthic diseases</subject><subject>Humans</subject><subject>IgG4 serology</subject><subject>Immunoglobulin G - blood</subject><subject>Infectious diseases</subject><subject>Loa - immunology</subject><subject>Loaiasis</subject><subject>loiasis</subject><subject>Loiasis - diagnosis</subject><subject>Loiasis - epidemiology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Parasitic diseases</subject><subject>Prevalence</subject><subject>Sensitivity and Specificity</subject><subject>Seroepidemiologic Studies</subject><subject>Tropical medicine</subject><issn>1360-2276</issn><issn>1365-3156</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1OwzAQRi0EKr9HQPICsUtwbGfqSGwQglIJxKawtVxnUlylMdgttDuOwBk5CUlbdc3KI39vPONHCM1YmjEJV9M0E5AnIsshzYpCpYxxLtPlHjnaBfvrmiWc9-GQHMc4ZYxJmUOP9ArgohDiiLwOJwNJIwZf-8mK-orW3pnoInUNnb8FRPrp6tpMcH1jGopNiTNnqQloOj76xfzt9_sHTZxjaOjAjH1zSg4qU0c8254n5OX-bnT7kDw-D4a3N4-JlZLLRBosrbKsQM4ZmJxVSgolKisB-DjnTCGzKHKAMfSxKLkCJouqD6VSTIERJ-Ry8-578B8LjHM9c9Fiu3CDfhF1v2h_qUC1oNqANvgYA1b6PbiZCSudMd0p1VPdmdOdOd0p1Wuletm2nm9nLMYzLHeNW4dtfrHNTbSmroJprIs7jHNoMWix6w325Wpc_Xu8Hj0N20L8AbZVkPw</recordid><startdate>199804</startdate><enddate>199804</enddate><creator>Touré, Fousseyni S.</creator><creator>Egwang, Thomas G.</creator><creator>Millet, Pascal</creator><creator>Bain, Odile</creator><creator>Georges, Alain J.</creator><creator>Wahl, Goetz</creator><general>Blackwell Science Ltd</general><general>Blackwell Science</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>199804</creationdate><title>IgG4 serology of loiasis in three villages in an endemic area of south‐eastern Gabon</title><author>Touré, Fousseyni S. ; 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international health</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Touré, Fousseyni S.</au><au>Egwang, Thomas G.</au><au>Millet, Pascal</au><au>Bain, Odile</au><au>Georges, Alain J.</au><au>Wahl, Goetz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IgG4 serology of loiasis in three villages in an endemic area of south‐eastern Gabon</atitle><jtitle>Tropical medicine &amp; international health</jtitle><addtitle>Trop Med Int Health</addtitle><date>1998-04</date><risdate>1998</risdate><volume>3</volume><issue>4</issue><spage>313</spage><epage>317</epage><pages>313-317</pages><issn>1360-2276</issn><eissn>1365-3156</eissn><abstract>Human filariasis due to Loa loa differs from other filariasis in that the majority of infected subjects are without circulating microfilariae (occult loiasis). In search for alternative diagnostic methods, which do not depend on circulating microfilariae or the (rather infrequent) eye‐passage of adult worms, it was shown earlier that IgG4 antibodies directed against Loa loa adult worm antigen are apparently a good marker of occult loiasis and specific with regard to the sympatrically occurring Mansonella perstans. In this study we evaluated an IgG4 antibody‐based ELISA using crude extract of Loa loa microfilariae (which is easier to obtain than adult worm) to estimate the prevalence of loiasis in 3 villages in South‐East Gabon. Of 222 examined individuals (80 children &lt; 16 years, 142 adults) 44 (20%) carried Loa loa microfilariae and 170 (77%) M. perstans. Using the mean OD‐value + 1 standard deviation of 9 sera from patients solely infected with M. perstans (from the Gambia, where Loa loa is not endemic) as a cut‐off, 35 of the 44 microfilaraemic Loa loa patients and 2 of the 9 Gambian controls were positive. This shows that our method had a sensitivity of 80% and a specificity of 78%. Among the remaining 178 subjects who had no microfilariae of Loa loa, as many as 97 (55%) had significant levels of specific IgG4 antibodies against Loa loa, suggesting that they carried occult loiasis. The mean IgG4 level in these putatively occult loiasis patients was slightly but significantly lower than in microfilaraemic subjects (P &lt; 0.03). In conclusion, despite the limited sensitivity and specificity of our method, IgG4‐ ELISA at present is a very useful tool in estimating the real prevalence of loiasis in epidemiological surveys and at the individual level can confirm the diagnosis of L. loa amicrofilaraemic subjects with clinical signs suggesting loiasis.</abstract><cop>Oxford BSL</cop><pub>Blackwell Science Ltd</pub><pmid>9623933</pmid><doi>10.1046/j.1365-3156.1998.00224.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Free Content; MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adolescent
Adult
Animals
Antibodies, Helminth - blood
Antibody Formation
Antigens, Helminth - immunology
Biological and medical sciences
Child
Diseases caused by nematodes
endemic villages
Enzyme-Linked Immunosorbent Assay
Female
Filariases
Gabon - epidemiology
Helminthic diseases
Humans
IgG4 serology
Immunoglobulin G - blood
Infectious diseases
Loa - immunology
Loaiasis
loiasis
Loiasis - diagnosis
Loiasis - epidemiology
Male
Medical sciences
Parasitic diseases
Prevalence
Sensitivity and Specificity
Seroepidemiologic Studies
Tropical medicine
title IgG4 serology of loiasis in three villages in an endemic area of south‐eastern Gabon
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