Publications by authors named "Luciana Raquel Vincenzi Fachin"

There is evidence that in southern US, leprosy is a zoonosis infecting wild Dasypus novemcinctus armadillos but the extent of this finding is unknown. This ecological study investigated leprosy in rural communities and in wild armadillos from the Brazilian Amazon. The study area was the Mamiá Lake of Coari municipality, Amazonas State, Northern region, a hyper endemic leprosy area where residents live on subsistence farming, fishing and armadillo hunting and its meat intake are frequent.

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Leprosy is a chronic infectious disease caused by Mycobacterium leprae. Previous studies have demonstrated that the difference among clinical forms of leprosy can be associated with the immune response of patients, mainly by T helper (Th) and regulatory T cells (Tregs). Then, aiming at clarifying the immune response, the expression of cytokines related to Th1, Th2, Th17 and Tregs profiles were evaluated by qPCR in 87 skin biopsies from leprosy patients.

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Article Synopsis
  • Leprosy, caused by Mycobacterium leprae, is a chronic infection mainly impacting the skin and nerves, with diagnosis traditionally based on clinical evaluation and supported by histopathological analysis.
  • A study analyzed 126 skin biopsies and 25 slit skin smears using quantitative PCR (qPCR) and routine bacilloscopy to compare diagnostic effectiveness, finding qPCR to be highly sensitive and specific.
  • The qPCR technique demonstrated 84.9% sensitivity in skin biopsies and 100% specificity, suggesting it is a reliable complementary diagnostic tool for leprosy across all clinical forms.
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In situ immunophenotyping of leprosy lesions can improve our understanding of the biology of inflammatory cells during the immune response to Mycobacterium leprae antigens. In the present study, biopsies from 10 healthy controls and 70 leprosy patients were selected, 10 for each of the following conditions: clinical tuberculoid (TT), borderline tuberculoid (BT), borderline borderline (BB), borderline lepromatous (BL), lepromatous (LL), reversal reaction (R1), and erythema nodosum leprosum (R2). Qualitative and quantitative immunohistochemical analyses were performed to detect CD3, CD4, CD8, FoxP3, CD20, CD138, CD1a, CD57, CD15, CD117, CD68, and CD163.

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