Profiling Human Serum Antibodies with a Carbohydrate Antigen Microarray

被引:147
作者
Oyelaran, Oyindasola [1 ]
McShane, Lisa M. [2 ]
Dodd, Lori [2 ]
Gildersleeve, Jeffrey C. [1 ]
机构
[1] NCI, Med Chem Lab, Ctr Canc Res, Frederick, MD 21702 USA
[2] NCI, Biometr Res Branch, Div Canc Treatment & Diag, Rockville, MD 20852 USA
关键词
Glycan array; carbohydrate antigens; serum antibodies; microarray; variability; normalization; CANCER-PATIENTS; BURKHOLDERIA-PSEUDOMALLEI; VACCINE DEVELOPMENT; GLYCAN MICROARRAY; IMMUNE-RESPONSES; ARRAY; TECHNOLOGY; EXPRESSION; LECTINS; CELLS;
D O I
10.1021/pr900515y
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Carbohydrate antigen arrays (glycan arrays) have been recently developed for the high-throughput analysis of carbohydrate macromolecule interactions. When profiling serum, information about experimental variability, interindividual biological variability, and intraindividual temporal variability is critical. In this report, we describe the characterization of a carbohydrate antigen array and assay for profiling human serum. Through optimization of assay conditions and development of a normalization strategy, we obtain highly reproducible results with a with in-experiment coefficient of variation (CV) of 10.8% and an overall CV (across multiple batches of slides and days) of 28.5%. We also report antibody profiles for 48 human subjects and evaluate for the first time the effects of age, race, sex, geographic location, and blood type on antibody profiles for a large set of carbohydrate antigens. We found significant dependence on age and blood type of antibody levels for a variety of carbohydrates. Finally, we conducted a longitudinal study with a separate group of 7 serum donors to evaluate the variation in anti-carbohydrate antibody levels within an individual over a period ranging from 3 to 13 weeks and found that, for nearly all antigens on our array, antibody levels are generally stable over this period. The results presented here provide the most comprehensive evaluation of experimental and biological variation reported to date for a glycan array and have significant implications for studies involving human serum profiling.
引用
收藏
页码:4301 / 4310
页数:10
相关论文
共 45 条
[1]   A RECEPTOR-MEDIATED IMMUNE-RESPONSE USING SYNTHETIC GLYCOCONJUGATES [J].
BERTOZZI, CR ;
BEDNARSKI, MD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1992, 114 (14) :5543-5546
[2]   Printed covalent glycan array for ligand profiling of diverse glycan binding proteins [J].
Blixt, O ;
Head, S ;
Mondala, T ;
Scanlan, C ;
Huflejt, ME ;
Alvarez, R ;
Bryan, MC ;
Fazio, F ;
Calarese, D ;
Stevens, J ;
Razi, N ;
Stevens, DJ ;
Skehel, JJ ;
van Die, I ;
Burton, DR ;
Wilson, IA ;
Cummings, R ;
Bovin, N ;
Wong, CH ;
Paulson, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (49) :17033-17038
[3]   Anticarbohydrate Antibody Repertoires in Patients Transplanted with Fetal Pig Islets Revealed by Glycan Arrays [J].
Blixt, O. ;
Kumagai-Braesch, M. ;
Tibell, A. ;
Groth, C. G. ;
Holgersson, J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2009, 9 (01) :83-90
[4]   Quantitation and characterization of anti-Galα1-3Gal antibodies in sera of 200 healthy persons [J].
Buonomano, R ;
Tinguely, C ;
Rieben, R ;
Mohacsi, PJ ;
Nydegger, UE .
XENOTRANSPLANTATION, 1999, 6 (03) :173-180
[5]   Selective tumor cell targeting using low-affinity, multivalent interactions [J].
Carlson, Coby B. ;
Mowery, Patricia ;
Owen, Robert M. ;
Dykhuizen, Emily C. ;
Kiessling, Laura L. .
ACS CHEMICAL BIOLOGY, 2007, 2 (02) :119-127
[6]  
Cekaite Lina, 2007, Methods Mol Biol, V360, P335
[7]  
Chen YT, 2005, METH MOLEC MED, V103, P207
[8]   USE OF SIALYLATED OR SULFATED DERIVATIVES AND ACRYLAMIDE COPOLYMERS OF GAL-BETA-1,3GALNAC-ALPHA- AND GALNAC-ALPHA- TO DETERMINE THE SPECIFICITIES OF BLOOD-GROUP T-SPECIFIC AND TN-SPECIFIC LECTINS AND THE COPOLYMERS TO MEASURE ANTI-T AND ANTI-TN ANTIBODY-LEVELS IN CANCER-PATIENTS [J].
CHEN, YX ;
JAIN, RK ;
CHANDRASEKARAN, EV ;
MATTA, KL .
GLYCOCONJUGATE JOURNAL, 1995, 12 (01) :55-62
[9]   Serum antibody screening by surface plasmon resonance using a natural glycan microarray [J].
de Boer, Arjen R. ;
Hokke, Cornelis H. ;
Deelder, Andre M. ;
Wuhrer, M. .
GLYCOCONJUGATE JOURNAL, 2008, 25 (01) :75-84
[10]  
Desai PR, 1997, ONKOLOGIE, V20, P472