Immunoassay standardization for the detection of immunoglobulin A (IgA) against Porphyromonas gingivalis antigens in saliva of individuals with and without leprosy
Mariana Costa Calheira,
Soraya Castro Trindade,
Michelle Miranda Lopes Falcão,
Luciana Sales Conceição Barbosa,
Gislene Regina Batista Carvalho,
Paulo Roberto Lima Machado,
Isaac Suzart Gomes-Filho,
Elisangela de Jesus Campos,
Paulo Cirino de Carvalho-Filho,
Márcia Tosta Xavier,
Antonio Pedro Fróes de Farias,
José Tadeu Raynal Rocha Filho,
Johelle de Santana Passos-Soares
Affiliations
Mariana Costa Calheira
Immunology Department, Federal University of Bahia
Soraya Castro Trindade
Immunology Department, Federal University of Bahia
Michelle Miranda Lopes Falcão
Immunology Department, Federal University of Bahia
Luciana Sales Conceição Barbosa
Immunology Department, Federal University of Bahia
Gislene Regina Batista Carvalho
Immunology Department, Federal University of Bahia
Paulo Roberto Lima Machado
Immunology Service, Professor Edgar Santos University Hospital, Federal University of Bahia
Isaac Suzart Gomes-Filho
Health Department, Feira de Santana State University
Elisangela de Jesus Campos
Oral Biochemistry Laboratory, Health Sciences Institute, Federal University of Bahia
Paulo Cirino de Carvalho-Filho
Dental School, Bahiana School of Medicine and Public Health
Márcia Tosta Xavier
Dental School, Bahiana School of Medicine and Public Health
Antonio Pedro Fróes de Farias
Immunology and Molecular Biology Laboratory, Federal University of Bahia
José Tadeu Raynal Rocha Filho
Immunology and Molecular Biology Laboratory, Federal University of Bahia
Johelle de Santana Passos-Soares
Immunology Department, Federal University of Bahia
Abstract Leprosy reactions are immune processes that cause neural damage in individuals with leprosy. As periodontitis is an infectious disease related to its development, specific antibodies to periodontal pathogens must be evaluated to better understand the humoral mechanisms underlying this relationship. Therefore, the objective of this study was to standardize an immunoassay to measure IgA specific to P. gingivalis antigens in the saliva of individuals with leprosy. An ELISA checkerboard titration was performed. A validation test involving 53 individuals with leprosy, 24 with and 19 without periodontitis, was conducted and a ROC curve constructed to calculate sensitivity and specificity. The coefficient of the optical densities was 2.21 and 2.66 for P. gingivalis crude extract and the recombinant protein HmuY, respectively. Sensitivity and specificity for the P. gingivalis crude extract were 66.7% and 73.7%, respectively, and for HmuY, were 62.5% and 52.6%, respectively. Specific recognition of P. gingivalis occurred predominantly in individuals with periodontitis, which validates the use of this test for studying periodontitis in individuals with leprosy. Trial registration CAEE 64476117.3.0000.0049, 21/07/2017, retrospectively registered