Spotlight on anti-CD25: daclizumab in MS.

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Spotlight on anti-CD25: daclizumab in MS. / Schippling, Sven; Martin, Roland.

In: Int MS J, Vol. 15, No. 3, 3, 2008, p. 94-98.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Schippling, S & Martin, R 2008, 'Spotlight on anti-CD25: daclizumab in MS.', Int MS J, vol. 15, no. 3, 3, pp. 94-98. <http://www.ncbi.nlm.nih.gov/pubmed/18808743?dopt=Citation>

APA

Schippling, S., & Martin, R. (2008). Spotlight on anti-CD25: daclizumab in MS. Int MS J, 15(3), 94-98. [3]. http://www.ncbi.nlm.nih.gov/pubmed/18808743?dopt=Citation

Vancouver

Schippling S, Martin R. Spotlight on anti-CD25: daclizumab in MS. Int MS J. 2008;15(3):94-98. 3.

Bibtex

@article{9dcc70d78f6a423a8a00510b5e4a80f0,
title = "Spotlight on anti-CD25: daclizumab in MS.",
abstract = "Monoclonal antibodies are a promising new class of therapeutic agents that can be employed to target specific molecules of the immune system or any tissue. They are currently being tested in a number of clinical trials in autoimmune diseases such as multiple sclerosis (MS). One of these, the humanized monoclonal anti-CD25 antibody daclizumab (Zenapax), is directed against the interleukin-2 (IL-2) receptor alpha chain (CD25) that is involved in clonal expansion of autoreactive T-cells by binding of its ligand IL- 2. Several years ago daclizumab was approved for the prevention of renal allograft rejection. Following promising observations in uveitis, daclizumab has since been tested in a number of small clinical trials in MS based on the rationale that blocking CD25 would prevent the expansion of autoreactive T-lymphocytes. Safety and efficacy data from the preliminary clinical exploration as well as findings about the mechanism of action of anti-CD25 treatment are reviewed here.",
author = "Sven Schippling and Roland Martin",
year = "2008",
language = "Deutsch",
volume = "15",
pages = "94--98",
number = "3",

}

RIS

TY - JOUR

T1 - Spotlight on anti-CD25: daclizumab in MS.

AU - Schippling, Sven

AU - Martin, Roland

PY - 2008

Y1 - 2008

N2 - Monoclonal antibodies are a promising new class of therapeutic agents that can be employed to target specific molecules of the immune system or any tissue. They are currently being tested in a number of clinical trials in autoimmune diseases such as multiple sclerosis (MS). One of these, the humanized monoclonal anti-CD25 antibody daclizumab (Zenapax), is directed against the interleukin-2 (IL-2) receptor alpha chain (CD25) that is involved in clonal expansion of autoreactive T-cells by binding of its ligand IL- 2. Several years ago daclizumab was approved for the prevention of renal allograft rejection. Following promising observations in uveitis, daclizumab has since been tested in a number of small clinical trials in MS based on the rationale that blocking CD25 would prevent the expansion of autoreactive T-lymphocytes. Safety and efficacy data from the preliminary clinical exploration as well as findings about the mechanism of action of anti-CD25 treatment are reviewed here.

AB - Monoclonal antibodies are a promising new class of therapeutic agents that can be employed to target specific molecules of the immune system or any tissue. They are currently being tested in a number of clinical trials in autoimmune diseases such as multiple sclerosis (MS). One of these, the humanized monoclonal anti-CD25 antibody daclizumab (Zenapax), is directed against the interleukin-2 (IL-2) receptor alpha chain (CD25) that is involved in clonal expansion of autoreactive T-cells by binding of its ligand IL- 2. Several years ago daclizumab was approved for the prevention of renal allograft rejection. Following promising observations in uveitis, daclizumab has since been tested in a number of small clinical trials in MS based on the rationale that blocking CD25 would prevent the expansion of autoreactive T-lymphocytes. Safety and efficacy data from the preliminary clinical exploration as well as findings about the mechanism of action of anti-CD25 treatment are reviewed here.

M3 - SCORING: Zeitschriftenaufsatz

VL - 15

SP - 94

EP - 98

IS - 3

M1 - 3

ER -