Monoclonal antibody ELISA to quantitate wheat gliadin contamination of gluten-free foods

1987 ◽  
Vol 98 (1) ◽  
pp. 123-127 ◽  
Author(s):  
A.R. Freedman ◽  
G. Galfrè ◽  
E. Gal ◽  
H.J. Ellis ◽  
P.J. Ciclitira
1987 ◽  
Vol 166 (2-3) ◽  
pp. 323-328 ◽  
Author(s):  
Andrew R. Freedman ◽  
Giovani Galfre ◽  
Eva Gal ◽  
H.Julia Ellis ◽  
Paul J. Ciclitira

Animals ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 358
Author(s):  
Morena Di Tommaso ◽  
Alessia Luciani ◽  
Paolo Emidio Crisi ◽  
Marica Beschi ◽  
Paolo Rosi ◽  
...  

Canine atopic dermatitis (CAD) is a pruritic allergic skin disease associated with IgE-mediated hypersensitivity. IgE is detected using Serum Allergen-Specific IgE test (SAT) in order to identify allergens. The present study aims to identify the environmental allergens in atopic dogs living in Northern Italy using SAT. The screening SAT (sSAT), using a monoclonal antibody cocktail-based ELISA to identify indoor and outdoor allergens, was performed. In all positive samples, an anti-IgE monoclonal antibody ELISA test was performed to extend panel of allergens. Out of 117 selected dogs, 69 were included in the study; 71% were positive and 29% were negative to sSAT. Among the 49 positive sSAT, 53% were positive for both indoor and outdoor, 38.8% only for indoor, and 8.2% only for outdoor allergens. This is the first study on the frequency of allergens involved in CAD in Italy using SAT. IgE hypersensitivity in atopic dogs of Northern Italy is usually associated with indoor allergens, primarily house dust mites. Among the outdoor allergens, an important role was played by Rumex acetosa. Polysensitization also commonly occurs. Therefore, since the numerous factors affect the IgE positivity in CAD, specific panels for geographical areas should be considered and re-evaluated at time intervals.


2002 ◽  
Vol 109 (1) ◽  
pp. S329-S329
Author(s):  
Juan A Asturias ◽  
Carmen Arilla ◽  
Ignacio Ibarrola ◽  
Elena Eraso ◽  
Jaime Algorta ◽  
...  

BMJ ◽  
1984 ◽  
Vol 289 (6437) ◽  
pp. 83-83 ◽  
Author(s):  
P J Ciclitira ◽  
H J Ellis ◽  
N L Fagg

2000 ◽  
Vol 66 (6) ◽  
pp. 2513-2519 ◽  
Author(s):  
Richard Kimura ◽  
Robert E. Mandrell ◽  
John C. Galland ◽  
Doreene Hyatt ◽  
Lee W. Riley

ABSTRACT Enterohemorrhagic Escherichia coli (EHEC) O157:H7 is an important food-borne pathogen in industrialized countries. We developed a rapid and simple test for detecting E. coli O157:H7 using a method based on restriction site polymorphisms. Restriction-site-specific PCR (RSS-PCR) involves the amplification of DNA fragments using primers based on specific restriction enzyme recognition sequences, without the use of endonucleases, to generate a set of amplicons that yield “fingerprint” patterns when resolved electrophoretically on an agarose gel. The method was evaluated in a blinded study of E. coli isolates obtained from environmental samples collected at beef cattle feedyards. The 54 isolates were all initially identified by a commonly used polyclonal antibody test as belonging to O157:H7 serotype. They were retested by anti-O157 and anti-H7 monoclonal antibody enzyme-linked immunosorbent assay (ELISA). The RSS-PCR method identified all 28 isolates that were shown to be E. coli O157:H7 by the monoclonal antibody ELISA as belonging to the O157:H7 serotype. Of the remaining 26 ELISA-confirmed non-O157:H7 strains, the method classified 25 strains as non-O157:H7. The specificity of the RSS-PCR results correlated better with the monoclonal antibody ELISA than with the polyclonal antibody latex agglutination tests. The RSS-PCR method may be a useful test to distinguish E. coli O157:H7 from a large number ofE. coli isolates from environmental samples.


Sign in / Sign up

Export Citation Format

Share Document