Skewed distribution of natural killer cells in psoriasis skin lesions

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Citações na Scopus
36
Tipo de produção
article
Data de publicação
2013
Título da Revista
ISSN da Revista
Título do Volume
Editora
WILEY-BLACKWELL
Autores
BATISTA, Mariana D.
HO, Emily L.
KUEBLER, Peter J.
MILUSH, Jeffrey M.
LANIER, Lewis L.
KALLAS, Esper G.
YORK, Vanessa A.
CHANG, David
LIAO, Wilson
UNEMORI, Patrick
Citação
EXPERIMENTAL DERMATOLOGY, v.22, n.1, p.64-66, 2013
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Psoriasis is a hyper-proliferative disease of the skin in which immunological mechanisms play a direct pathogenetic role. There have been limited studies of natural killer (NK) cells in psoriasis. The aim of this study was to examine the phenotype of NK cells in skin biopsies and peripheral blood mononuclear cells from patients with psoriasis and healthy controls. CD56+CD16- and CD56+CD16+ NK cells were isolated from lesional skin, unaffected skin and PBMC of psoriasis patients, and normal skin and PBMC from healthy controls. The expression of CD57, NKG2A and NKG2C was assessed by flow cytometry. NK cells in psoriasis skin lesions were skewed in their expression of CD57, a marker of NK cell maturity, with CD57 expression significantly reduced and NKG2A expression increased on NK cells in lesional and unaffected skin compared to controls. These data suggest that in this patient cohort, NK cells could be isolated from psoriasis lesions and exhibit an immature phenotype.
Palavras-chave
CD57, immunosenescence, natural killer cells, psoriasis
Referências
  1. Beziat V, 2010, PLOS ONE, V5, DOI 10.1371/journal.pone.0011966
  2. Bjorkstrom NK, 2010, BLOOD, V116, P3853, DOI 10.1182/blood-2010-04-281675
  3. Brenchley JM, 2003, BLOOD, V101, P2711, DOI 10.1182/blood-2002-07-2103
  4. CALIGIURI MA, 1990, J EXP MED, V171, P1509, DOI 10.1084/jem.171.5.1509
  5. Cameron AL, 2003, BRIT J DERMATOL, V149, P160, DOI 10.1046/j.1365-2133.2003.05319.x
  6. Dunphy S, 2011, J BIOMED BIOTECHNOL, DOI 10.1155/2011/248317
  7. Hong HS, 2010, J VIROL, V84, P1183, DOI 10.1128/JVI.01675-09
  8. Lopez-Verges S, 2011, P NATL ACAD SCI USA, V108, P14725, DOI 10.1073/pnas.1110900108
  9. Lopez-Verges S, 2010, BLOOD, V116, P3865, DOI 10.1182/blood-2010-04-282301
  10. Nestle FO, 2009, NEW ENGL J MED, V361, P496, DOI 10.1056/NEJMra0804595
  11. Orr MT, 2010, CELL, V142, P847, DOI 10.1016/j.cell.2010.08.031
  12. Ottaviani C, 2006, EUR J IMMUNOL, V36, P118, DOI 10.1002/eji.200535243
  13. Sun JC, 2011, IMMUNOL CELL BIOL, V89, P327, DOI 10.1038/icb.2010.162
  14. Suzuki Y, 2004, J INVEST DERMATOL, V122, P1133, DOI 10.1111/j.0022-202X.2004.22517.x
  15. Tobin AM, 2011, J INNATE IMMUN, V3, P403, DOI 10.1159/000328011