Monoclonal antibodies to equine IgM improve the sensitivity of West Nile virus-specific IgM detection in horses.
Abstract: West Nile virus (WNV) is a zoonotic pathogen of global importance. In horses with neurological signs, detection of WNV-specific immunoglobulin M (IgM) in serum is widely used to identify clinical cases of WNV encephalitis. Here, we describe the development of two monoclonal antibodies (mAbs) to equine IgM which were used in a WNV IgM-specific enzyme-linked immunosorbent assay (ELISA). Their performance was compared to an established assay based on polyclonal anti-IgM. Check test serum samples from the National Veterinary Service Laboratory (NVSL) were used to evaluate the performance of the three anti-IgM antibodies. The anti-IgM 1-22 mAb correctly identified all NVSL samples. Both the polyclonal antibody and monoclonal anti-IgM 2B-63 identified eight out of ten samples correctly. The three assays were then compared using serum samples from clinically healthy animals (n=33) and horses with neurological signs (n=21). High Spearman rank correlations (0.76-0.86) were found among the ELISA results. Inter-test agreements (weighted kappa) for assay interpretation resulted in strong agreement (0.95) of the results obtained by the mAbs and moderate agreements when monoclonal and polyclonal anti-IgM-based assays were compared. To determine the analytical sensitivities of anti-WNV IgM detection, serial dilutions of WNV IgM-positive serum samples were analyzed. The highest sensitivity was obtained by using the anti-IgM 1-22 mAb to capture IgM from equine serum. In conclusion, the use of monoclonal anti-IgM antibodies can improve the sensitivity of IgM detection in the acute phase of WN disease.
Publication Date: 2007-12-03 PubMed ID: 18054390DOI: 10.1016/j.vetimm.2007.10.013Google Scholar: Lookup
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- Journal Article
- Clinical Pathology
- Comparative Study
- Diagnosis
- Diagnostic Technique
- Disease Diagnosis
- Enzyme-Linked Immunosorbent Assay (ELISA)
- Epidemiology
- Equine Diseases
- Equine Health
- Horses
- Immunoglobulin M
- Immunology
- Infection
- Infectious Disease
- Monoclonal Antibodies
- Neurological Diseases
- Serum
- Veterinary Medicine
- Virus
- West Nile Virus
- Zoonotic Diseases
Summary
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The research article is about the development of two monoclonal antibodies for equine IgM that improves the sensitivity of West Nile Virus-specific IgM detection in horses.
Objective and Methodology of the Research
- The main purpose of this study was to design two specific monoclonal antibodies (mAbs) that target equine Immunoglobulin M (IgM), and to compare their efficiency with a previously established polyclonal anti-IgM assay in identifying West Nile Virus (WNV) in horses.
- An enzyme-linked immunosorbent assay (ELISA) was used as the detection method. ELISA is a popular laboratory method for measuring antibodies or antigens in a sample. It has high sensitivity and provides quantitative results.
- Test serum samples from the National Veterinary Service Laboratory (NVSL) were used to assess the performance of the three anti-IgM antibodies. These samples acted as a standard or check measure.
Performance Metrics and Results
- The two monoclonal antibodies and the polyclonal anti-IgM were tested on serum samples taken from clinically healthy animals (n=33) and horses showing neurological symptoms (n=21).
- The monoclonal antibody, anti-IgM 1-22, correctly identified all NVSL samples. The other two antibodies, the polyclonal antibody, and the monoclonal anti-IgM 2B-63 identified eight out of ten samples correctly.
- The researchers determined the analytical sensitivities of anti-WNV IgM detection by analyzing serial dilutions of WNV IgM-positive serum samples. Here, the highest sensitivity was achieved using the anti-IgM 1-22 monoclonal antibody.
- The ELISA results from the three anti-IgM antibodies were statistically analyzed showing high Spearman rank correlations (0.76-0.86), indicating a strong similarity in their rankings of the samples.
- Inter-test agreements (weighted kappa) for the assay interpretation showed strong agreement (0.95) of results obtained by the monoclonal antibodies and moderate agreements when the monoclonal and polyclonal anti-IgM-based assays were compared.
Conclusion
- The research concluded that using monoclonal anti-IgM antibodies can increase the sensitivity of WNV-specific IgM detection in the early stage of West Nile disease in horses. This is important in diagnosing the disease early and starting treatment, which can mitigate the damage caused by the disease and improve the prognosis.
Cite This Article
APA
Wagner B, Glaser A, Hillegas JM, Erb H, Gold C, Freer H.
(2007).
Monoclonal antibodies to equine IgM improve the sensitivity of West Nile virus-specific IgM detection in horses.
Vet Immunol Immunopathol, 122(1-2), 46-56.
https://doi.org/10.1016/j.vetimm.2007.10.013 Publication
Researcher Affiliations
- Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA. bw73@cornell.edu
MeSH Terms
- Animals
- Antibodies, Anti-Idiotypic / immunology
- Antibodies, Monoclonal / immunology
- Antibodies, Viral / blood
- Enzyme-Linked Immunosorbent Assay
- Horses / immunology
- Immunoglobulin G / blood
- Immunoglobulin M / blood
- Sensitivity and Specificity
- West Nile virus / immunology
Citations
This article has been cited 8 times.- Zhang Z, Yao Y, Yang J, Jiang H, Meng Y, Cao W, Zhou F, Wang K, Yang Z, Yang C, Sun J, Yang Y. Assessment of adaptive immune responses of dairy cows with Burkholderia contaminans-induced mastitis.. Front Microbiol 2023;14:1099623.
- Raza F, Babasyan S, Larson EM, Freer HS, Schnabel CL, Wagner B. Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses.. PLoS One 2021;16(5):e0252243.
- Patel RS, Tomlinson JE, Divers TJ, Van de Walle GR, Rosenberg BR. Single-cell resolution landscape of equine peripheral blood mononuclear cells reveals diverse cell types including T-bet(+) B cells.. BMC Biol 2021 Jan 22;19(1):13.
- Goodrich EL, McLean A, Guarino C. A Pilot Serosurvey for Selected Pathogens in Feral Donkeys (Equus asinus).. Animals (Basel) 2020 Oct 2;10(10).
- Carossino M, Wagner B, Loynachan AT, Cook RF, Canisso IF, Chelvarajan L, Edwards CL, Nam B, Timoney JF, Timoney PJ, Balasuriya UBR. Equine Arteritis Virus Elicits a Mucosal Antibody Response in the Reproductive Tract of Persistently Infected Stallions.. Clin Vaccine Immunol 2017 Oct;24(10).
- Yeh JY, Lee JH, Park JY, Seo HJ, Moon JS, Cho IS, Kim HP, Yang YJ, Ahn KM, Kyung SG, Choi IS, Lee JB. A diagnostic algorithm to serologically differentiate West Nile virus from Japanese encephalitis virus infections and its validation in field surveillance of poultry and horses.. Vector Borne Zoonotic Dis 2012 May;12(5):372-9.
- Ledermann JP, Lorono-Pino MA, Ellis C, Saxton-Shaw KD, Blitvich BJ, Beaty BJ, Bowen RA, Powers AM. Evaluation of widely used diagnostic tests to detect West Nile virus infections in horses previously infected with St. Louis encephalitis virus or dengue virus type 2.. Clin Vaccine Immunol 2011 Apr;18(4):580-7.
- Lewis MJ, Wagner B, Irvine RM, Woof JM. IgA in the horse: cloning of equine polymeric Ig receptor and J chain and characterization of recombinant forms of equine IgA.. Mucosal Immunol 2010 Nov;3(6):610-21.
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