Serum Geoepidemiology of Leprosy Biomarkers in a City-Wide COVID-19 Survey in Brazil
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Background COVID-19 has created a significant global health emergency and triggered numerous seroepidemiological field tracing initiatives. The use of these samples becomes a timely tool for intensifying active case finding and early diagnosis of leprosy. This study aimed to evaluate the humoral immune response against the Mce1A and PGL-I antigens of M. leprae , thereby contributing to the clarification of the disease and facilitating the tracking of cases, which in turn enables spatial mapping. Methods A cross-sectional and geoepidemiological study was carried out using the biorepository of samples from the COVID-19 serosurvey in a municipality in southeastern Brazil. Screening diagnosis using LSQ and the artificial intelligence system MaLeSQs® was applied to investigate neurodermatological signs and symptoms of leprosy (n = 224). IgA, IgM, and IgG anti-Mce1A and IgM anti-PGL-I antibodies were measured using indirect ELISA (n = 195). Georeferencing was employed to create the distribution maps of individuals within the municipality. Global spatial autocorrelation analysis was performed and applied to the serological scores. Results The responses to the clinical questionnaire reported the predominance of neurological signs and symptoms. Twelve new cases were diagnosed (32.4%), and the detection rate in the population sample evaluated was 6.15%. The IgA anti-Mce1A ELISA showed the highest seropositivity (55.3%), the highest rates [median = 0.93 (IQR = 0.59–1.41)]. The IgM and IgG anti-Mce1A serology showed higher rates (P < 0.0001) as compared to the anti-PGL-I serology. The overlap of positivity with the antibodies tested highlights the greater involvement of double or triple positives when Mce1A serology was used. IgM anti-Mce1A serology was positive in 66.7% [8/12 cases; median = 1.25 (IQR = 0.70–1.68)] of new cases detected. Serology with the IgA antibody presented the highest rates in georeferencing analysis and served as an alert for contact with the bacillus. The sociodemographic variables tested did not exhibit statistical difference in spatial autocorrelation (p > 0.05), indicating the absence of a spatially clustered pattern for serological values in the analyzed territory. Conclusion The study showed a diffuse pattern of transmission and exposure to leprosy in the municipality. The study highlights the benefits of using serological screening tools with new biomarkers and digital technology platforms for the early diagnosis of leprosy.