Characterization of cytotoxic immune response in skin and mucosal lesions of paracoccidioidomycosis |
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Authors: | Carla Pagliari Naiura Vieira Pereira Luciane Kanashiro Felipe Weisshaupt Stegun Julio Croda Maria Irma Seixas Duarte Mirian Nacagami Sotto |
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Institution: | 1. Laboratory of the Discipline of Pathology of Transmissible Diseases, Department of Pathology, Faculty of Medical Sciences, University of S?o Paulo, Sao Paulo, Brazil;2. Laboratory of Dermatopathology, Department of Dermatology, Faculty of Medical Sciences, University of S?o Paulo, Sao Paulo, Brazil;3. Faculty of Health Sciences, University of Grande Dourados, Dourados, Brazil |
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Abstract: | Background: CD8+ T cells and natural killer (NK) cells are involved in the immune response against some pathogens. For this purpose, we investigated the in situ paracoccidioidomycosis (PCM) immune response addressing the participation of NK cells, CD8+ T cells, perforin and granzyme B expression. Methods: Sixty biopsies of PCM skin and mucosa were classified according to the presence of compact granulomas (G1), poorly organized granulomas (G2) and both kinds in the same lesion (G3). CD8+ T cells, NK cells, perforin and granzyme B were showed by immunohistochemistry. Results: CD8+ T cells were increased over NK cells in cutaneous G1 and G2 lesions. There was no difference regarding such cells in G3 lesions, although they were abundant in such lesions. In mucosa, CD8+ T cells were increased in number over NK cells in all groups. Granzyme B in skin increased in G2 and G3. The number of granzyme did not differ in mucosal lesions in the three groups. Conclusions: CD8+ T cells and NK cells play a role in PCM cutaneous and mucosal lesions. The predominance of CD8+ T cells over NK cells may represent an effective response against the fungi. Moreover, the high number of granzyme B expressing cells corroborates this possibility. Pagliari C, Pereira NV, Kanashiro L, Stegun FW, Croda J, Seixas Duarte MI, Sotto MN. Characterization of cytotoxic immune response in skin and mucosal lesions of paracoccidioidomycosis. |
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