BackgroundPathogenesis of psoriasis is complex. Latest evidences suggest the role of T-lymphocytes (CD4+, CD8+, and CD45RO+ memory T cells), Langerhans cells (CD1a+) and VEGF in the altered keratinocytes kinetics.
Aims and objectivesTo evaluate the extent of infiltration of T-lymphocytes (CD4+, CD8+, CD45RO+), Langerhans cells (CD1a+) and VEGF in lesional and non lesional skin in psoriatic patients and healthy controls.
Materials and methodsTwenty-five untreated psoriasis cases were taken up for study. Five millimeter biopsies of the patient's skin were taken from the newest Psoriasis Lesion (PL) and the farthest non-lesional skin (PN). They were stained with H&E (Hematoxylin and Eosin stain) and with monoclonal antibody against CD4+, CD8+, CD45RO+ T cells, CD1a+ and VEGF. Skin biopsies of 5 healthy controls were also subjected to the same stain.
ResultsOn hematoxylin and eosin staining, the degree of cellular infiltrate was more in PL dermis than PL epidermis, while similar degree of cellular infiltrate was found in PN epidermis and dermis. Dermal vascular proliferation was also higher in PL than in PN. On immunohistochemical evaluation, epidermal infiltrate of CD4+ T cells, CD8+ T cells and CD1a+ cells were more abundant in PL than in PN. Also, VEGF was more expressed in the epidermis of PL than in PN. However, CD45RO+ T cells were more in the dermis of PL than in PN. When comparing PL and PN with healthy controls, there was increased infiltration of all markers when compared to controls.
ConclusionThe inflammatory process in psoriasis involves the whole skin of the patient, but is more pronounced in the damaged skin.