Haemostasis-maintaining platelets are also recognized as important modulators in the regulation of immune response. Activated platelets expressing
P-selectin (CD62P) are involved in the extravasation of leucocytes. This study evaluated platelet
P-selectin expression as a
biomarker for cutaneous
inflammation.
P-selectin expression was assessed by flow cytometry in 147 successive patients suffering from an inflammatory or infectious skin condition at the day of admission for in-patient treatment as well as a day prior to demission. Forty-one patients admitted for
allergy testing served as controls. A commercially available ELISA was used in 17 patients to determine soluble
P-selectin in the plasma. In patients with
psoriasis, the
Psoriasis Area and Severity Index (PASI) was documented as a measure for disease severity. We observed a significant increase in platelet
P-selectin expression in patients with inflammatory or infectious disorders, when compared to the control group (3,01% vs. 1,46%; P < 0.000001). Successful treatment resulted in a significant decrease in
P-selectin expression to the level of the control group. In the case of
psoriasis (n = 47), we found highly significant correlation between
P-selectin and PASI (r = 0.51; P < 0.000001), as well as between the change in the PASI and the change in
P-selectin expression (r = 0.4; P = 0.006). Platelet
P-selectin expression as determined by flow cytometry correlated well with the results of soluble
P-selectin, determined by ELISA (r = 0.63; P < 0.01). Thus, platelet
P-selectin expression may be used as an efficacy
biomarker to monitor treatment success in
psoriasis. As platelet
P-selectin correlates with soluble
P-selectin in patient plasma, which can be measured by ELISA, the latter is feasible also for routine use.