Oral lesions in lupus erythematosus-cytokines profiles of inflammatory infiltrate


Autoria(s): MARQUES, Elisa R. M. C.; LOURENCO, Silvia Vanessa; LIMA, Dirce M.; NICO, Marcello Menta S.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Background: Lupus erythematosus (LE) is a chronic inflammatory disease. Presence of type 1 cytokines in cutaneous discoid lesions suggests that they may be critical for induction, development and maintenance of these manifestations. Type 2 cytokines in combination with local interferon gamma (INF-gamma) are thought to be related to the physiopathology of cutaneous LE. Cytokines profiles are still unknown in oral LE lesions. Materials and Methods: Expression of Th1 and Th2 cytokines (including IL-4, IL-5, IL-6, IL-10, IL-12, tumor necrosis factor alpha (TNF-alpha) and INF-gamma was investigated and compared in 29 biopsies of intra-oral (sun-protected) and labial lesions (sun-exposed) of LE using immunohistochemistry. Results: Inflammatory infiltrate of LE lesions was strongly positive for IFN-gamma (97%) and TNF-alpha (90%), both Th1 type cytokines. Interleukin-10, a Th2 cytokine was also strongly expressed. Other cytokines were only mildly positive. Cytokines patterns were similar in intra-oral (sun-covered) and labial (sun-exposed) LE lesions. Conclusions: Oral LE lesions are associated with both type 1 and type 2 cytokines, characterized by stronger expression of INF-gamma, TNF-alpha and IL-10. These findings suggest that although ultraviolet (UV) light is involved in the induction of LE lesions, mechanisms of lesions formation may be similar in sun-exposed as well as sun-covered areas.

Identificador

JOURNAL OF CUTANEOUS PATHOLOGY, v.37, n.4, p.439-445, 2010

0303-6987

http://producao.usp.br/handle/BDPI/23086

10.1111/j.1600-0560.2009.01424.x

http://dx.doi.org/10.1111/j.1600-0560.2009.01424.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL PUBLISHING, INC

Relação

Journal of Cutaneous Pathology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL PUBLISHING, INC

Palavras-Chave #BLOOD MONONUCLEAR-CELLS #TUMOR-NECROSIS-FACTOR #CUTANEOUS LUPUS #IMMUNOHISTOCHEMICAL PROFILE #ULTRAVIOLET-LIGHT #MESSENGER-RNA #SKIN-LESIONS #FACTOR-ALPHA #PATHOGENESIS #DISEASE #Dermatology #Pathology
Tipo

article

original article

publishedVersion