Author:
Chamian Francesca,Lin Shao-Lee,Lee Edmund,Kikuchi Toyoko,Gilleaudeau Patricia,Sullivan-Whalen Mary,Cardinale Irma,Khatcherian Artemis,Novitskaya Inna,Wittkowski Knut M,Krueger James G,Lowes Michelle A
Abstract
Abstract
Background
Alefacept (anti-CD2) biological therapy selectively targets effector memory T cells (Tem) in psoriasis vulgaris, a model Type 1 autoimmune disease.
Methods
Circulating leukocytes were phenotyped in patients receiving alefacept for moderate to severe psoriasis.
Results
In all patients, this treatment caused a preferential decrease in effector memory T cells (CCR7- CD45RA-) (mean 63% reduction) for both CD4+ and CD8+ Tem, while central memory T cells (Tcm) (CCR7+CD45RA-) were less affected, and naïve T cells (CCR7+CD45RA+) were relatively spared. Circulating CD8+ effector T cells and Type 1 T cells (IFN-γ-producing) were also significantly reduced.
Conclusion
Alefacept causes a selective reduction in circulating effector memory T cells (Tem) and relative preservation of central memory T cells (Tcm) in psoriasis.
Publisher
Springer Science and Business Media LLC
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
Cited by
63 articles.
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