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Series GSE27293 Query DataSets for GSE27293
Status Public on Feb 21, 2013
Title An antibody leukocyte capture microarray in diagnosis of Systemic Lupus Erythematosus
Organism Homo sapiens
Experiment type Protein profiling by protein array
Summary The diagnosis of Systemic Lupus Erythematosus (SLE) is challenging due to its heterogeneous clinical presentation and lack of robust biomarkers for laboratory testing to distinguish it from other autoimmune or infectious diseases. Current diagnostic criterion relies on a combination of clinical examination and laboratory tests, and it does not readily distinguish between those with active clinical disease from those that are clinically quiescent. Several groups have attempted to apply emerging high throughput profiling technologies to diagnose SLE. Despite showing promising diagnostic potential, many of them are expensive and technically challenging for routine clinical uses. Here we report a pilot study of applying a technically simple and highly customisable leukocyte capture antibody microarray to profile healthy (n=24) and SLE patients (n=60) of various disease activities. Our analysis reveals a set of surface antigen biomarkers that have significant association with SLE. In addition, we present a computational method to calculate a score from the entire microarray profile to obtain a score that correlate most reliably with SLE disease activity. Although the current version of our microarray alone does not match the discriminatory power of the standard laboratory tests (serum dsDNA, complements C3 and C4), the combination of the two yields a test with significantly increased discriminatory ability than what can be achieved individually. This work paves the way for a customised SLE-specific antibody microarray for accurate diagnosis and monitoring of SLE that can be readily translated to routine clinical use.
 
Overall design Blood samples were collected from 60 patients of Systemic Lupus Erythematosus (SLE) of different disease activity (11 active, 16 semi-active, and 33 inactive), and compared it with blood samples from 24 healthy blood donors. For each subject, we extracted PBMCs and apply them to a leukocyte capture antibody microarray. The microarray was then scaned by a DotScan™ slide reader (Medsaic; Eveleigh, NSW, Australia). The number of immobilized cells was proportional to the light scattered at each antibody spot. Binding of PBMCs to each antibody dot was monitored by light scatter and averaged between the duplicate spots on each slide. We then performed statistical analysis to identify CD antigen markers that are associated with SLE, as well as determining the potential diagnostic ability of this microarray for SLE.
 
Contributor(s) Lin M, Ho JW, Harrison L, dos Remedios CG, Adelstein S
Citation(s) 23516448
Submission date Feb 14, 2011
Last update date Mar 25, 2013
Contact name Joshua WK Ho
E-mail jwho@rics.bwh.harvard.edu
Organization name Brigham and Women's Hospital
Department Department of Medicine
Lab Division of Genetics
Street address 41 Avenue Louis Pasteur
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL13165 Medsaic Human DotScan antibody microarray v3
Samples (134)
GSM674849 120571_SLE_active
GSM674850 120664_SLE_active
GSM674851 120554_SLE_active
Relations
BioProject PRJNA137343

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE27293_rawdata.xls.gz 123.8 Kb (ftp)(http) XLS
Raw data is available on Series record
Processed data included within Sample table

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