A novel chemistry for conjugating pneumococcal polysaccharides to Luminex microspheres

被引:69
作者
Schlottmann, SA [1 ]
Jain, N [1 ]
Chirmule, N [1 ]
Esser, MT [1 ]
机构
[1] Merck Res Labs, Vaccine & Biol Res, Wayne, PA 19087 USA
关键词
Luminex; PNEUMOVAX((R))23; DMTMM; vaccine;
D O I
10.1016/j.jim.2005.11.019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we describe a novel method to conjugate pneumococcal polysaccharides (PnPS) to Luminex microspheres for use in serological assays. 4-(4,6-dimethoxy[1,3,5]triazin-2-yl)-4-methyl-morpholinium (DMTMM) modification of PnPS and conjugation to carboxyl functional groups on Luminex microspheres (COOH-DMTMM method) was shown to be a reproducible chemistry that efficiently conjugated PnPS to Luminex microspheres without affecting the antigenicity of a broad set of PnPS. The COOH-DMTMM method was compared to three other methods for robustness, reproducibility and effect on PnPS antigenicity in a multiplexed assay format. The other methods examined included adsorption of the unmodified PnPS to Luminex microspheres, oxidation of the PnPS to conjugate them to amino-modified microspheres using carbodiimide chemistry and poly-L-lysine modification of the PnPS before conjugating to carboxy Luminex microspheres using carbodiimide chemistry. Of the four methods, the COOH-DMTMM chemistry was shown to be a robust methodology, producing stable PnPS coupled microspheres with a 4-log dynamic range and low cross-reactivity when used in a PnPS-specific IgG serology assay. This novel chemistry should be useful for developing serological assays to measure antibodies to polysaccharides for use in vaccine and epidemiology studies. (c) 2006 Published by Elsevier B.V.
引用
收藏
页码:75 / 85
页数:11
相关论文
共 27 条
[1]   Comparison of a multiplexed fluorescent covalent microsphere immunoassay and an enzyme-linked immunosorbent assay for measurement of human immunoglobulin G antibodies to anthrax toxins [J].
Biagini, RE ;
Sammons, DL ;
Smith, JP ;
MacKenzie, BA ;
Striley, CAF ;
Semenova, V ;
Steward-Clark, E ;
Stamey, K ;
Freeman, AE ;
Quinn, CP ;
Snawder, JE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2004, 11 (01) :50-55
[2]   Method for simultaneous measurement of antibodies to 23 pneumococcal capsular polysaccharides [J].
Biagini, RE ;
Schlottmann, SA ;
Sammons, DL ;
Smith, JP ;
Snawder, JC ;
Striley, CAF ;
MacKenzie, BA ;
Weissman, DN .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2003, 10 (05) :744-750
[3]  
*CDC, 1997, MMWR-MORBID MORTAL W, P46
[4]  
*CDC, 2000, MMWR-MORBID MORTAL W, P49
[5]   Evaluation of previously assigned antibody concentrations in pneumococcal polysaccharide reference serum 89SF by the method of cross-standardization [J].
Concepcion, N ;
Frasch, CE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1998, 5 (02) :199-204
[6]   Pneumococcal type 22F polysaccharide absorption improves the specificity of a pneumococcal-polysaccharide enzyme-linked immunosorbent assay [J].
Concepcion, NF ;
Frasch, CE .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2001, 8 (02) :266-272
[7]   A comparison of ELISA and flow micro sphere-based assays for quantification of immunoglobulins [J].
Dasso, J ;
Lee, J ;
Bach, H ;
Mage, RG .
JOURNAL OF IMMUNOLOGICAL METHODS, 2002, 263 (1-2) :23-33
[8]   Quantitative, multiplexed detection of bacterial pathogens:: DNA and protein applications of the Luminex LabMAP™ system [J].
Dunbar, SA ;
Vander Zee, CA ;
Oliver, KG ;
Karem, KL ;
Jacobson, JW .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 53 (02) :245-252
[9]   Report from a workshop on multianalyte microsphere assays [J].
Earley, MC ;
Vogt, RF ;
Shapiro, HM ;
Mandy, FF ;
Kellar, KL ;
Bellisario, R ;
Pass, KA ;
Marti, GE ;
Stewart, CC ;
Hannon, WH .
CYTOMETRY, 2002, 50 (05) :239-242
[10]   Efficacy of a pneumococcal conjugate vaccine against acute otitis media [J].
Eskola, J ;
Kilpi, T ;
Palmu, A ;
Jokinen, J ;
Haapakoski, J ;
Herva, E ;
Takala, A ;
Käyhty, H ;
Karma, P ;
Kohberger, R ;
Siber, G ;
Mäkela, PH ;
Lockhart, S ;
Ecrola, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (06) :403-409