Nuclear fluorescence serum reactivity on monkey oesophagus: a new antibody for the follow-up of coeliac disease

• Published in: Clinical and experimental immunology Vol. 161; no. 3; pp. 417 - 425
• Main Authors: Picarelli, A, Sabbatella, L, Di Tola, M, Silano, M, Nicolussi, A, D'Inzeo, S, Coppa, A
• Format: Journal Article
• Language: English
• Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01.09.2010; Blackwell Publishing Ltd; Blackwell; Oxford University Press; Blackwell Science Inc
• Subjects: Adolescent; Adult; Analytical, structural and metabolic biochemistry; Animals; anti-endomysium; Antibody Specificity - immunology; Autoantibodies - blood; Autoantibodies - immunology; Autoantibodies - metabolism; Biological and medical sciences; Caco-2 Cells; celiac disease; Celiac Disease - blood; Celiac Disease - diagnosis; Celiac Disease - immunology; coeliac disease; Esophagus - immunology; Female; Fluorescence; Fluorescent Antibody Technique, Indirect - methods; follow-up; Follow-Up Studies; Fundamental and applied biological sciences. Psychology; Gastroenterology. Liver. Pancreas. Abdomen; gluten-free diet; Haplorhini; Humans; Immunoglobulin A - blood; Immunoglobulin A - immunology; Intestine, Small - immunology; Intestine, Small - metabolism; Male; Medical sciences; Middle Aged; nuclear fluorescence reactivity; Organ Culture Techniques; Other diseases. Semiology; Serum - immunology; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Translational Studies; Young Adult; Deficient diet; Monkey; Fluorescence; Biochemistry; Coeliac disease; nuclear fluorescence reactivity; follow-up; Intestinal malabsorption; Primates; Intestinal disease; Serum; Immunopathology; gluten-free diet; Digestive system; Antibody; Feeding; Esophagus; anti-endomysium; Vertebrata; Mammalia; Reactivity; Endomysium; Follow up study; Animal; Digestive diseases
• ISSN: 0009-9104; 1365-2249
• DOI: 10.1111/j.1365-2249.2010.04184.x

We have identified previously a nuclear fluorescence reactivity (NFR) pattern on monkey oesophagus sections exposed to coeliac disease (CD) patients' sera positive for anti-endomysium antibodies (EMA). The aim of the present work was to characterize the NFR, study the time-course of NFR-positive results in relation to gluten withdrawal and evaluate the potential role of NFR in the follow-up of CD. Twenty untreated, 87 treated CD patients and 15 healthy controls were recruited and followed for 12 months. Their sera were incubated on monkey oesophagus sections to evaluate the presence of NFR by indirect immunofluorescence analysis. Duodenal mucosa samples from treated CD patients were challenged with gliadin peptides, and thus the occurrence of NFR in culture supernatants was assessed. The NFR immunoglobulins (Igs) reactivity with the nuclear extract of a human intestinal cell line was investigated. Serum NFR was present in all untreated CD patients, persisted up to 151 ± 37 days from gluten withdrawal and reappeared in treated CD patients under dietary transgressions. Serum NFR was also detected in two healthy controls. In culture supernatants of coeliac intestinal mucosa challenged with gliadin peptides, NFR appeared before EMA. The Igs responsible for NFR were identified as belonging to the IgA2 subclass. The NFR resulted differently from EMA and anti-nuclear antibodies, but reacted with two nuclear antigens of 65 and 49 kDa. A new autoantibody, named NFR related to CD, was described. Furthermore, NFR detection might become a valuable tool in monitoring adherence to a gluten-free diet and identifying slight dietary transgressions.