Detection of Antibody against Fungal Glucosylceramide in Immunocompromised Patients: A Potential New Diagnostic Approach for Cryptococcosis

被引:6
作者
Qureshi, Asfia [1 ]
Wray, Dannah [2 ]
Rhome, Ryan [1 ]
Barry, William [2 ]
Del Poeta, Maurizio [1 ,2 ,3 ,4 ]
机构
[1] Med Univ S Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Div Infect Dis, Charleston, SC 29425 USA
[3] Med Univ S Carolina, Dept Microbiol & Immunol, Charleston, SC 29425 USA
[4] Med Univ S Carolina, Dept Craniofacial Biol, Charleston, SC 29425 USA
基金
美国国家卫生研究院;
关键词
Glucosylceramide; Antibody; ELISA; HIV; Cryptococcosis; Fungal infection;
D O I
10.1007/s11046-011-9485-8
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have developed an ELISA to determine the value of anti-glucosylceramide antibody for the prediction of disseminated cryptococcosis in immunocompromised subjects and performed a clinical prospective study at the Medical University of South Carolina. The study enrolled a total of 53 patients who were free of active fungal diseases at the time of enrollment but at risk of developing one because they were all immunocompromised, e.g., (1) patients positive for HIV and (2) patients post- or awaiting solid organ transplantation. Among 53 patients enrolled, two patients developed invasive cryptococcosis, and in both patients, IgM anti-GlcCer was detected in sera using the ELISA at least 6 weeks prior to the clinical presentation of the brain disease. These results were corroborated by a cryptococcal antigen lateral flow assay, which was also positive in serum prior to the development of meningoencephalitis. However, a high number of positive results were also detected in patients with no evidence of cryptococcosis. This study highlights the potential utility of this new assay in early diagnostic testing algorithms for patients at risk for cryptococcosis, but further investigations are needed to validate the sensitivity and specificity of the glucosylceramide ELISA as a predictor of cryptococcosis.
引用
收藏
页码:419 / 425
页数:7
相关论文
共 19 条
[1]  
BENDER BS, 1988, REV INFECT DIS, V10, P1142
[2]   CHEMOTAXIS OF HUMAN-NEUTROPHILS AND MONOCYTES INDUCED BY CRYPTOCOCCUS-NEOFORMANS [J].
DIAMOND, RD ;
ERICKSON, NF .
INFECTION AND IMMUNITY, 1982, 38 (01) :380-382
[3]  
Diaz MR, 2011, CRYPTOCOCCUS HUMAN P
[4]  
Dropulic LK, 2009, DIAGNOSTIC MICROBIOL
[5]  
Irwin M, 2001, BR MED J
[6]   Roles for inositol-phosphoryl ceramide synthase 1 (IPC1) in pathogenesis of C-neoformans [J].
Luberto, C ;
Toffaletti, DL ;
Wills, EA ;
Tucker, SC ;
Casadevall, A ;
Perfect, JR ;
Hannun, YA ;
Del Poeta, M .
GENES & DEVELOPMENT, 2001, 15 (02) :201-212
[7]   Systematic screens of a Candida albicans homozygous deletion library decouple morphogenetic switching and pathogenicity [J].
Noble, Suzanne M. ;
French, Sarah ;
Kohn, Lisa A. ;
Chen, Victoria ;
Johnson, Alexander D. .
NATURE GENETICS, 2010, 42 (07) :590-U166
[8]   Disruption of the sphingolipid Δ8-desaturase gene causes a delay in morphological changes in Candida albicans [J].
Oura, Takahiro ;
Kajiwara, Susumu .
MICROBIOLOGY-SGM, 2008, 154 :3795-3803
[9]   Candida albicans sphingolipid C9-methyltransferase is involved in hyphal elongation [J].
Oura, Takahiro ;
Kajiwara, Susumu .
MICROBIOLOGY-SGM, 2010, 156 :1234-1243
[10]  
Perfect JR., 2006, Molecular principles of fungal pathogenesis, P3