Abstract | BACKGROUND: 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.
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Authors | Francesca Chamian, Shao-Lee Lin, Edmund Lee, Toyoko Kikuchi, Patricia Gilleaudeau, Mary Sullivan-Whalen, Irma Cardinale, Artemis Khatcherian, Inna Novitskaya, Knut M Wittkowski, James G Krueger, Michelle A Lowes |
Journal | Journal of translational medicine
(J Transl Med)
Vol. 5
Pg. 27
(Jun 07 2007)
ISSN: 1479-5876 [Electronic] England |
PMID | 17555598
(Publication Type: Clinical Trial, Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Antigens, CD
- Antigens, Differentiation, T-Lymphocyte
- CD2 Antigens
- CD69 antigen
- Dermatologic Agents
- Lectins, C-Type
- Recombinant Fusion Proteins
- Alefacept
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Topics |
- Adult
- Aged
- Alefacept
- Antigens, CD
(immunology)
- Antigens, Differentiation, T-Lymphocyte
(immunology)
- CD2 Antigens
(immunology)
- Cell Movement
(drug effects)
- Dermatologic Agents
(administration & dosage, therapeutic use)
- Female
- Humans
- Immunologic Memory
(drug effects)
- Lectins, C-Type
- Lymphocyte Activation
(drug effects, immunology)
- Lymphocyte Count
- Lymphocyte Subsets
(drug effects, pathology)
- Male
- Middle Aged
- Phenotype
- Psoriasis
(drug therapy, immunology, pathology)
- Recombinant Fusion Proteins
(administration & dosage, pharmacology, therapeutic use)
- T-Lymphocytes
(drug effects, immunology, pathology)
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