{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,9,4]],"date-time":"2024-09-04T05:54:40Z","timestamp":1725429280236},"reference-count":35,"publisher":"Oxford University Press (OUP)","issue":"1","license":[{"start":{"date-parts":[[2007,4,11]],"date-time":"2007-04-11T00:00:00Z","timestamp":1176249600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2007,4,25]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Innate immune system deficiency may predispose to severe infections such as Legionnaires' disease. We have investigated the role of mannose-binding lectin (MBL) deficiency in the Melbourne Aquarium Legionnaires' disease outbreak. Serum samples from patients and controls that were exposed but shown to be uninfected from the Melbourne Aquarium Legionnaires' disease outbreak were tested for MBL function (C4 deposition) and level (mannan-binding). MBL function was lower in Legionnaires' disease cases than in age- and sex-matched uninfected, exposed controls. The frequency of MBL deficiency with C4 deposition &amp;lt;\u20030\u00b72\u2003U\/\u00b5l was significantly higher in Legionnaires' disease cases than in controls. This also applied to Legionnaires' disease cases requiring hospital care. There was no difference in MBL mannan-binding levels between Legionnaires' disease patients and controls. There was no significant interval change in MBL function or level after a mean of 46\u2003days. MBL complement activation functional deficiency appears to predispose to Legionnaires' disease.<\/jats:p>","DOI":"10.1111\/j.1365-2249.2007.03390.x","type":"journal-article","created":{"date-parts":[[2010,8,12]],"date-time":"2010-08-12T14:14:55Z","timestamp":1281622495000},"page":"97-102","source":"Crossref","is-referenced-by-count":17,"title":["Low mannose-binding lectin complement activation function is associated with predisposition to Legionnaires' disease"],"prefix":"10.1093","volume":"149","author":[{"given":"D P","family":"Eisen","sequence":"first","affiliation":[{"name":"Clinical Centre for Research Excellence in Infectious Diseases, Victorian Infectious Diseases Service, Royal Melbourne Hospital, Parkville, Victoria, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Stubbs","sequence":"additional","affiliation":[{"name":"Clinical Centre for Research Excellence in Infectious Diseases, Victorian Infectious Diseases Service, Royal Melbourne Hospital, Parkville, Victoria, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D","family":"Spilsbury","sequence":"additional","affiliation":[{"name":"Cooperative Research Centre for Vaccine Technology at Australian Red Cross Blood Service, Brisbane, Queensland, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Carnie","sequence":"additional","affiliation":[{"name":"Department of Human Services, Victoria, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J","family":"Leydon","sequence":"additional","affiliation":[{"name":"Victorian Infectious Diseases Reference Laboratory, North Melbourne, Victoria, Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B P","family":"Howden","sequence":"additional","affiliation":[{"name":"Australian Bacterial Pathogenesis Program, Department of Microbiology, Monash University, Clayton, Victoria, Australia"},{"name":"Infectious Diseases 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