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FTY720 therapy exerts differential effects on T cell subsets in multiple sclerosis
Oleh:
Mehling, M.
;
Brinkmann, V.
;
Antel, J.
Jenis:
Article from Journal - ilmiah internasional
Dalam koleksi:
Neurology (Official Journal of The American Academy of Neurology) vol. 71 no. 16 (Oct. 2008)
,
page 1261-1267.
Topik:
LYMPH NODE
;
PHYCOERYTHRIN
Ketersediaan
Perpustakaan FK
Nomor Panggil:
N11.K.2008.04
Non-tandon:
1 (dapat dipinjam: 0)
Tandon:
tidak ada
Lihat Detail Induk
Isi artikel
Background: The oral immunomodulator FTY720 has shown efficacy in patients with relapsing multiple sclerosis (MS). FTY720 functionally antagonizes sphingosine 1-phosphate receptor-1 (S1P1) on T cells and consequently inhibits S1P/S1P1-dependent lymphocyte egress from secondary lymphoid organs. Little is known about the phenotype and function of T cells remaining in peripheral blood during long-term FTY720 treatment. Methods: T cells from FTY720-treated, interferon-beta (IFNß)-treated and untreated patients with MS, and healthy donors (HD) were analyzed with respect to T cell subpopulation composition, proliferation, and cytokine production. Results: In FTY720-treated patients (n = 16), peripheral blood CD4+ and CD8+ T cell counts were reduced by approximately 80% and 60% when compared to the other groups (IFNß: n = 7; untreated: n = 5; HD: n = 10). This related to selective reduction of naïve (CCR7+CD45RA+) and central memory (CCR7+CD45RA–) T cells (TCM), and resulted in a relative increase of peripheral effector memory (CCR7–CD45RA– [TEM] and CCR7–CD45RA+ [TEMRA]) T cells. The remaining blood T cell populations displayed a reduced potential to secrete IL-2 and to proliferate in vitro, but rapidly produced interferon-gamma upon reactivation, confirming a functional TEM/TEMRA phenotype. Neither FTY720 nor FTY720-P directly suppressed proliferation or cytokine production by T cells. Conclusion: Therapeutic dosing of FTY720 reduces naïve T cells and TCM, but not TEM, in blood, without affecting T cell function. This is presumably because naïve T cells and TCM express the homing receptor CCR7, allowing recirculation to secondary lymphoid tissues on a regular basis and, thus, trapping of the cells by FTY720 in lymph nodes.
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