Paracoccidioides brasiliensis interacts with dermal dendritic cells and keratinocytes in human skin and oral mucosa lesions

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Citações na Scopus
6
Tipo de produção
article
Data de publicação
2016
Título da Revista
ISSN da Revista
Título do Volume
Editora
OXFORD UNIV PRESS
Citação
MEDICAL MYCOLOGY, v.54, n.4, p.370-376, 2016
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Paracoccidioidomycosis (PCM) is a systemic disease caused by the fungus Paracoccidioides brasiliensis and Paracoccidioides lutzii. In PCM the skin and oral mucosa are often affected. Dendritic cells and keratinocytes of the integument play a role in innate and adaptive immune response against pathogens, due to their function as antigen presenting cells. Aiming to verify the interaction of P. brasiliensis with these cell populations, we studied 52 skin and 47 oral mucosa samples taken from patients with proven diagnosis of PCM. The biopsies were subjected to immunohistochemical and/or immunofluorescence staining with anti-factor XIIIa (marker of dermal dendrocytes), anti-CD207 (marker ofmature Langerhans cells), anti-pan cytokeratins (AE1-AE3) and anti-P. brasiliensis antibodies. Analyses with confocal laser microscopy were also performed for better visualization of the interaction between keratinocytes and the fungi. In sum, 42% of oral mucosa samples displayed yeast forms in Factor XIIIa dermal dendrocytes cytoplasm. Langerhans cells in skin and oral mucosa samples did not show yeast cells in their cytoplasm. In sum, 54% of skin and 60% of mucosal samples displayed yeast cells in the cytoplasm of keratinocytes. The parasitism of keratinocytes may represent a possible mechanism of evasion of the fungus to local immune mechanisms. Factor XIIIa dendrocytes and keratinocytes may be acting as antigen-presenting cells to fulfill the probably impaired function of Langerhans cells in skin and oral mucosa of human PCM.
Palavras-chave
Paracoccidioidomycosis, dendritic cells, keratinocytes, immunohistochemistry, confocal laser microscopy, skin and oral mucosa
Referências
  1. Nestle FO, 1998, J INVEST DERMATOL, V110, P762, DOI 10.1046/j.1523-1747.1998.00189.x
  2. NICKOLOFF BJ, 1993, AM J PATHOL, V143, P325
  3. Kuo IH, 2013, J ALLERGY CLIN IMMUN, V131, P266, DOI 10.1016/j.jaci.2012.12.1563
  4. Heath WR, 2013, NAT IMMUNOL, V14, P978, DOI 10.1038/ni.2680
  5. Valladeau J, 2005, SEMIN IMMUNOL, V17, P273, DOI 10.1016/j.smim.2005.05.009
  6. Asahina A, 2006, J DERMATOL SCI, V44, P1, DOI 10.1016/j.jdermsci.2006.07.002
  7. da Silva RP, 2011, J MED MICROBIOL, V60, P269, DOI 10.1099/jmm.0.022467-0
  8. Paquet P, 2000, AM J DERMATOPATH, V22, P413, DOI 10.1097/00000372-200010000-00005
  9. GIMENEZ MF, 1987, ARCH DERMATOL, V123, P479, DOI 10.1001/archderm.123.4.479
  10. Moreto TC, 2011, T ROY SOC TROP MED H, V105, P473, DOI 10.1016/j.trstmh.2011.03.001
  11. Pagliari C, 2003, AM J DERMATOPATH, V25, P107, DOI 10.1097/00000372-200304000-00003
  12. Merad M, 2009, BLOOD, V113, P3418, DOI 10.1182/blood-2008-12-180646
  13. Sotto MN, 2010, AM J DERMATOPATH, V32, P15, DOI 10.1097/DAD.0b013e3181ab4695
  14. Quatresooz P, 2008, INT J MOL MED, V22, P403, DOI 10.3892/ijmm_00000036
  15. Pagliari C, 2002, MED MYCOL, V40, P407, DOI 10.1080/714031129
  16. Sotto MN, 2004, J CUTAN PATHOL, V31, P14, DOI 10.1046/j.0303-6987.2004.0131.x
  17. de Brito T, 1973, Virchows Arch A Pathol Pathol Anat, V361, P129
  18. CERIO R, 1989, BRIT J DERMATOL, V121, P421, DOI 10.1111/j.1365-2133.1989.tb15509.x
  19. Franco M, 1987, Rev Soc Bras Med Trop, V20, P129
  20. Pagliari C, 2013, MICROBES INFECT, V13, P1012
  21. Sandoval M, 1996, INT J SURG PATHOL, V3, P181
  22. Theodoro RC, 2012, PLOS ONE, V7, DOI 10.1371/journal.pone.0037694