TY - JOUR
T1 - Successful in vivo blockade of CD25 (high-affinity interleukin 2 receptor) on T cells by administration of humanized anti-Tac antibody to patients with psoriasis
AU - Krueger, James G.
AU - Walters, Ian B.
AU - Miyazawa, Megumi
AU - Gilleaudeau, Patricia
AU - Hakimi, John
AU - Light, Susan
AU - Sherr, Amelia
AU - Gottlieb, Alice B.
N1 - Funding Information:
Supported in part by a General Clinical Research Center Grant (M01-RR00102) from the National Center for Research Resources at the National Institutes of Health (NIH); by NIH grant AI39214; and by a grant from Hoffmann-LaRoche, Inc.
PY - 2000
Y1 - 2000
N2 - Background: Daclizumab is a humanized antibody to the α-subunit (CD25) of the interleukin 2 (IL-2) receptor that blocks normal IL-2 binding to this receptor. Because IL-2 is a major stimulus for T-cell growth, blockade of the IL-2 receptor could be useful in treating T-cell-mediated (autoimmune) diseases. Objective: Our purpose was to determine whether adequate concentrations of antibody were achieved in circulating blood and in psoriatic skin lesions to saturate CD25 receptors. We also intended to measure clinical effect and safety of this agent when used alone (without other immunosuppressive drugs) in psoriasis. Methods: Nineteen patients with psoriasis in two centers received daclizumab at an initial dose of 2 mg/kg, then 1 mg/kg at weeks 2, 4, 8, and 12. To determine whether CD25 was blocked in vivo, flow cytometric studies measured (1) expression of CD25 on CD3+ T cells derived from blood and (2) immunohistochemistry measures of CD25+ cells done on pretreatment and posttreatment biopsy specimens. Patients were followed up clinically with photographs and Psoriasis Area and Severity Index scores. Results: This study showed a consistent blockade of CD25 in peripheral blood and tissue during the first 4 weeks of therapy while the dosing was every 2 weeks. Variable desaturation of receptors began after 4 weeks, which correlated with a reversal in disease improvement. Patients with a pretreatment Psoriasis Area and Severity Index score of less than 36 showed a mean reduction in severity by 30% at 8 weeks (P = .02). During the 16 weeks of treatment, a 44.8% decrease in expression of the IL-2 receptor α-subunit was found. The absolute T-cell counts were calculated and showed no significant changes during the course of the study No significant adverse events were produced by daclizumab during this study. Conclusion: We therefore conclude that daclizumab is a well-tolerated agent that blocks CD25 expression in peripheral blood and skin. Furthermore, it may be useful in treating psoriasis in some patients.
AB - Background: Daclizumab is a humanized antibody to the α-subunit (CD25) of the interleukin 2 (IL-2) receptor that blocks normal IL-2 binding to this receptor. Because IL-2 is a major stimulus for T-cell growth, blockade of the IL-2 receptor could be useful in treating T-cell-mediated (autoimmune) diseases. Objective: Our purpose was to determine whether adequate concentrations of antibody were achieved in circulating blood and in psoriatic skin lesions to saturate CD25 receptors. We also intended to measure clinical effect and safety of this agent when used alone (without other immunosuppressive drugs) in psoriasis. Methods: Nineteen patients with psoriasis in two centers received daclizumab at an initial dose of 2 mg/kg, then 1 mg/kg at weeks 2, 4, 8, and 12. To determine whether CD25 was blocked in vivo, flow cytometric studies measured (1) expression of CD25 on CD3+ T cells derived from blood and (2) immunohistochemistry measures of CD25+ cells done on pretreatment and posttreatment biopsy specimens. Patients were followed up clinically with photographs and Psoriasis Area and Severity Index scores. Results: This study showed a consistent blockade of CD25 in peripheral blood and tissue during the first 4 weeks of therapy while the dosing was every 2 weeks. Variable desaturation of receptors began after 4 weeks, which correlated with a reversal in disease improvement. Patients with a pretreatment Psoriasis Area and Severity Index score of less than 36 showed a mean reduction in severity by 30% at 8 weeks (P = .02). During the 16 weeks of treatment, a 44.8% decrease in expression of the IL-2 receptor α-subunit was found. The absolute T-cell counts were calculated and showed no significant changes during the course of the study No significant adverse events were produced by daclizumab during this study. Conclusion: We therefore conclude that daclizumab is a well-tolerated agent that blocks CD25 expression in peripheral blood and skin. Furthermore, it may be useful in treating psoriasis in some patients.
UR - http://www.scopus.com/inward/record.url?scp=0033857240&partnerID=8YFLogxK
U2 - 10.1067/mjd.2000.106515
DO - 10.1067/mjd.2000.106515
M3 - Article
AN - SCOPUS:0033857240
SN - 0190-9622
VL - 43
SP - 448
EP - 458
JO - Journal of the American Academy of Dermatology
JF - Journal of the American Academy of Dermatology
IS - 3
ER -