Publication: Immunohistochemical assessment of cell populations in leprosy-spectrum lesions and reactional forms
Authors
Fachin, Luciana Raquel Vincenzi ; Soares, Cleverson Teixeira ; Belone, Andrea de Faria Fernandes ; Trombone, Ana Paula Favaro ; Rosa, Patrícia Sammarco ; Guidella, Cássio Cesar ; Franco, Marcello Fabiano
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-804
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info:eu-repo/semantics/article
Description
Abstract
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. In addition, histochemistry was employed to
identify eosinophils. The amount of CD3+ and CD4+ T
cells was higher in TT than in LL patients. CD8+ T cells
were predominant in T lymphocyte infiltrations in the
basal layer of the epidermis. The number of FoxP3+ cells
was similar among different forms of the disease, but
was higher in BL and LL than in R2 individuals. CD20+
lymphocytes were most abundant in TT samples, while
CD138+ plasma cells displayed no detectable
differences. Epithelioid macrophages from the center of
TT and R1 granulomas exhibited the M1 phenotype
(CD68+CD163-
), whereas those in LL granulomas
showed the M2 phenotype (CD68+CD163+). There was
a gradual decrease in the amount of CD1a+ cells from
the TT towards the LL form of the disease. A significant
increase in the number of neutrophils was observed only
in R2 samples. All the cells investigated, except
eosinophils, participated in the immunopathogenesis of
leprosy.
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Citation
Histology and Histopathology, Vol.32, nº4, (2017)
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