Mannose-binding lectin serum levels and (Gly54asp) gene polymorphism in recurrent aphthous stomatitis: A case-control study

Author:

Baioumy Shereen A1,Fouad Shaimaa H2ORCID,Abdalgeleel Shaimaa A3,Baiomy Ahmed A4,Sallam Dina E5,Taha Sara I6ORCID

Affiliation:

1. Department of Microbiology and Immunology, Faculty of Medicine, Zagazig University, Zagazig, Egypt

2. Department of Internal Medicine / Allergy and Clinical Immunology, Ain Shams University, Cairo, Egypt

3. Department of Biostatistics and Epidemiology, National Cancer Institute, Cairo University, Cairo, Egypt

4. Department of Fixed prosthodontics, Egyptian Russian University, Badr City, Egypt

5. Department of Pediatrics & Pediatric Nephrology, Faculty of Medicine, Ain-Shams University, Cairo, Egypt

6. Department of Clinical Pathology/ Immunology, Faculty of Medicine, Ain Shams University, Cairo, Egypt

Abstract

Objectives: Dysregulation of the immune response appears to play a significant role in recurrent aphthous stomatitis (RAS) development. The main objective of this case–control study is to investigate the blood levels of mannose-binding lectin (MBL) and the frequency of the MBL2 gene (gly54asp) polymorphism in RAS patients, including 40 RAS patients and 40 healthy controls. Methods: Serum MBL levels were determined by ELISA, while the PCR-restriction fragment length polymorphism was used in MBL2 genotyping. Results: The median serum MBL level was significantly lower in the RAS group than in the control group (975 ng/mL (545–1320) vs. 1760 ng/mL (1254–2134); p≤ 0.001). The MBL levels were significantly lower in the BB genotype, whereas they were significantly higher in the wild type AA with a median of 525 and 1340 ng/mL, respectively ( p =0.005). The B allele was expressed in significantly higher percentages of RAS patients than in controls. There was no significant association between MBL serum levels ( p=0.685) or MBL2 codon 54 genotypes ( p=0.382) with the type of ulcers. Conclusion: There was an association between low MBL serum levels and the variant allele B of the MBL2 (gly54asp) gene, and the susceptibility to RAS. As a result, potential novel therapeutic options for RAS patients with MBL deficiency should be investigated.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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