Analysis of CD15, CD57 and HIF-1α in biopsies of patients with peri-implantitis

• Published in: Pathology, research and practice research and practice, 2017-09, Vol.213 (9), p.1097-1101
• Main Authors: de Araújo, Márcia Fernandes, Etchebehere, Renata Margarida, de Melo, Marcelo Luiz Ribeiro, Beghini, Marcela, Severino, Viviane Oliveira, de Castro Côbo, Eliângela, Rocha Rodrigues, Denise Bertulucci, de Lima Pereira, Sanívia Aparecida
• Format: Article
• Language: English
• Subjects: Aged; Biomarkers - analysis; Biopsy; CD15; CD57; CD57 Antigens - analysis; CD57 Antigens - biosynthesis; Cross-Sectional Studies; Dental Implants - adverse effects; Female; Fucosyltransferases - analysis; Fucosyltransferases - biosynthesis; HIF-1α; Humans; Hypoxia-Inducible Factor 1, alpha Subunit - analysis; Hypoxia-Inducible Factor 1, alpha Subunit - biosynthesis; Immunohistochemistry; Lewis X Antigen - analysis; Lewis X Antigen - biosynthesis; Male; Middle Aged; Peri-implantitis; Peri-Implantitis - immunology; Stomatitis - immunology
• ISSN: 0344-0338; 1618-0631
• DOI: 10.1016/j.prp.2017.07.020

Peri-implantitis is an infectious disease characterized by inflammation of the tissues surrounding the implant, bleeding on probing with or without suppuration, and bone loss. Peri-implant lesions contain a leukocyte infiltrate of plasma cells, lymphocytes, macrophages and neutrophils. A survey of the literature did not show any studies reporting an association between hypoxia and peri-implantitis. The aim of the present cross-sectional study was to evaluate histological changes and immunostaining for CD15, CD57 and HIF-1α in the peri-implant mucosa of patients with and without peri-implantitis. Mucosal biopsies were obtained from 18 patients with peri-implantitis and 10 control subjects without peri-implantitis at a private health care center between 2010 and 2012. The sections were fixed in 10% buffered formalin, processed and embedded in paraffin for histopathological and immunohistochemical study. Acanthosis, spongiosis and exocytosis were observed in both groups, with no significant difference between them. The peri-implantitis group showed increased immunostaining for CD15, a neutrophil marker, and HIF-1α, a tissue hypoxia marker, but no significant difference in immunostaining for CD57, a Natural Killer cell marker. The increase in neutrophil (CD15) and hypoxia (HIF-1α) markers in patients with peri-implantitis suggests an active participation of neutrophils and hypoxia in the pathogenesis of this disease. Since the present study was the first to evaluate the expression of CD15, CD57 and HIF-1α in peri-implant tissues, further studies should be performed to better understand the role of these molecules in peri-implantitis.