Alefacept (anti-CD2) causes a selective reduction in circulating effector memory T cells (Tem) and relative preservation of central memory T cells (Tcm) in psoriasis. Academic Article uri icon

Overview

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-gamma-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.

publication date

  • June 7, 2007

Research

keywords

  • CD2 Antigens
  • Cell Movement
  • Immunologic Memory
  • Psoriasis
  • Recombinant Fusion Proteins
  • T-Lymphocytes

Identity

PubMed Central ID

  • PMC1906741

Scopus Document Identifier

  • 34447329553

Digital Object Identifier (DOI)

  • 10.1097/00007890-199208000-00018

PubMed ID

  • 17555598

Additional Document Info

volume

  • 5