Association of lectin pathway proteins with intra-abdominal Candida infection in high-risk surgical intensive-care unit patients. A prospective cohort study within the fungal infection network of Switzerland. Issue 3 (March 2016)

• Record Type: Journal Article
• Authors: Bregenzer, Thomas; Conen, Anna; Fankhauser, Hans; Flückiger, Ursula; Khanna, Nina; Frei, Reno; Heininger, Ulrich; Hertel, Roland; Franciolli, Mario; San Giovanni, Ospedale; Dolina, Marisa; Rothen, Madeleine; Dubuis, Olivier; Tarr, Philipp; Graf, Suzanne; Fleisch, Felix; Risch, Martin; Ritzler, Eva; Chuard, Christian; Erard, Véronique; Fracheboud, Dominique; Emonet, Stéphane; Genne, Daniel; Lienhardt, Reto; Chave, Jean-Philippe; Andreutti-Zaugg, Corinne; Gallusser, Alberto; Graber, Peter; Monotti, Rita; Bernasconi, Enos; Krause, Martin; Herzog, Karin; Piso, Rein-Jan; Schibli, Urs; Bally, Frank; Troillet, Nicolas; Tissière, Lysiane; Boggian, Katja; Bruderer, Thomas; Gubler, Jacques; Eich, Gerhard; Berger, Christoph; Osthoff, Michael; Wojtowicz, Agnieszka; Tissot, Frederic; Jørgensen, Clara; Thiel, Steffen; Zimmerli, Stephan; Marchetti, Oscar; Khanna, Nina; Bochud, Pierre-Yves; Trendelenburg, Marten;
• Is Part Of: Journal of infection. Volume 72:Issue 3(2016)
• Page Start: 377
• Page End: 385
• Publication Date: 2016-03
• Subjects: Complement system -- Mannose-binding lectin -- Ficolins -- Candida infections -- Intensive-care unit; Infection -- Periodicals; Bacterial Infections -- Periodicals; Communicable Diseases -- Periodicals; Electronic journals; 616.905
• DOI: 10.1016/j.jinf.2015.12.011
• Languages: English
• ISSNs: 0163-4453

Abstract

Summary: Objectives: Human studies on the role of mannose-binding lectin (MBL) in patients with invasive candidiasis have yielded conflicting results. We investigated the influence of MBL and other lectin pathway proteins on Candida colonization and intra-abdominal candidiasis (IAC) in a cohort of high-risk patients. Methods: Prospective observational cohort study of 89 high-risk intensive-care unit (ICU) patients. Levels of lectin pathway proteins at study entry and six MBL2 single-nucleotide polymorphisms were analyzed by sandwich-type immunoassays and genotyping, respectively, and correlated with development of heavy Candida colonization (corrected colonization index (CCI) ≥0.4) and occurrence of IAC during a 4-week period. Results: Within 4 weeks after inclusion a CCI ≥0.4 and IAC was observed in 47% and 38% of patients respectively. Neither serum levels of MBL, ficolin-1, -2, -3, MASP-2 or collectin liver 1 nor MBL2 genotypes were associated with a CCI ≥0.4. Similarly, none of the analyzed proteins was found to be associated with IAC with the exception of lower MBL levels (HR 0.74, p = 0.02) at study entry. However, there was no association of MBL deficiency (<0.5 μg/ml), MBL2 haplo- or genotypes with IAC. Conclusion: Lectin pathway protein levels and MBL2 genotype investigated in this study were not associated with heavy Candida colonization or IAC in a cohort of high-risk ICU patients. Highlights: Mannose-binding lectin has been shown to bind to Candida albicans. Lectin complement proteins were evaluated in high-risk intensive-care unit patients. Lectin protein levels were not associated with Candida colonization or infection. Mannose-binding lectin genotype was not associated with Candida infection.