AJTMH HINARI
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am. J. Trop. Med. Hyg., 58(5), 1998, pp. 543-550
Copyright © 1998 by The American Society of Tropical Medicine and Hygiene

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nibbeling, H.
Right arrow Articles by Deelder, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nibbeling, H.
Right arrow Articles by Deelder, A.
Related Collections
Right arrow Schistosomiasis
American Journal of Tropical Medicine and Hygiene, Vol 58, Issue 5, 543-550
Copyright © 1998 by American Society of Tropical Medicine and Hygiene

Research Articles


Use of monoclonal antibodies prepared against Schistosoma mansoni hatching fluid antigens for demonstration of Schistosoma haematobium circulating egg antigens in urine

HA Nibbeling, AI Kahama, RJ Van Zeyl, and AM Deelder

A panel of 17 monoclonal antibodies (MAbs) against Schistosoma soluble egg antigens (SEAs) was produced from BALB/c mice immunized with antigens secreted/excreted by Schistosoma mansoni eggs. In this study, we demonstrate that 16 MAbs were reactive with S. haematobium SEA in addition to S. mansoni SEA. The MAbs were tested as potential immunodiagnostic reagents in a homologous sandwich ELISA format to detect circulating soluble egg antigens (CSEAs) in serum and urine samples of S. mansoni- or S. haematobium-infected individuals. When samples of S. mansoni-infected individuals were tested, none of these MAbs performed as good as the previously described S. mansoni-specific 114-5B1-A and 114-4D12-A MAbs. However, 11 MAbs (of the IgM isotype) detected CSEA in urine samples of S. haematobium-infected individuals. Three MAbs, 290-2E6-A, 291-3D5-A, and 291-5D5-A, were selected for a pilot study with 47 urine samples of S. haematobium-infected individuals from Kenya. The CSEA levels detected with each of these ELISAs showed a significant correlation with urinary egg counts (Spearman rho > 0.37, P < 0.01) and with each other (Spearman rho > 0.74, P < 0.001). Based on the 92% specificity and 90% sensitivity of the assay, the ELISA using MAb 290-2E6-A was found to be the most promising assay for immunodiagnosis of S. haematobium infections.


This article has been cited by other articles:


Home page
Clin Med ResHome page
P. M. Neal
Schistosomiasis - An Unusual Cause of Ureteral Obstruction: A Case History and Perspective
Clin. Med. Res., November 1, 2004; 2(4): 216 - 227.
[Abstract] [Full Text] [PDF]


Home page
Infect. Immun.Home page
A. van Remoortere, G. J. van Dam, C. H. Hokke, D. H. van den Eijnden, I. van Die, and A. M. Deelder
Profiles of Immunoglobulin M (IgM) and IgG Antibodies against Defined Carbohydrate Epitopes in Sera of Schistosoma-Infected Individuals Determined by Surface Plasmon Resonance
Infect. Immun., April 1, 2001; 69(4): 2396 - 2401.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
A. v. Remoortere, C. H.Hokke, G. J.v. Dam, I. v. Die, A. M.Deelder, and D. H.v. d. Eijnden
Various stages of Schistosoma express Lewisx, LacdiNAc, GalNAc{beta}1-4 (Fuc{alpha}1-3)GlcNAc and GalNAc{beta}1-4(Fuc{alpha}1-2Fuc{alpha}1-3)GlcNAc carbohydrate epitopes: detection with monoclonal antibodies that are characterized by enzymatically synthesized neoglycoproteins
Glycobiology, June 1, 2000; 10(6): 601 - 609.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1998 by the American Society of Tropical Medicine and Hygiene.