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Ultra low-dose IL-2 for GVHD prophylaxis after allogeneic hematopoietic stem cell transplantation mediates expansion of regulatory T cells without diminishing antiviral and antileukemic activity.


ABSTRACT: GVHD after allogeneic hematopoietic stem cell transplantation (alloSCT) has been associated with low numbers of circulating CD4(+)CD25(+)FoxP3(+) regulatory T cells (Tregs). Because Tregs express high levels of the interleukin (IL)-2 receptor, they may selectively expand in vivo in response to doses of IL-2 insufficient to stimulate T effector T-cell populations, thereby preventing GVHD.We prospectively evaluated the effects of ultra low-dose (ULD) IL-2 injections on Treg recovery in pediatric patients after alloSCT and compared this recovery with Treg reconstitution post alloSCT in patients without IL-2. Sixteen recipients of related (n = 12) or unrelated (n = 4) donor grafts received ULD IL-2 post hematopoietic stem cell transplantation (HSCT; 100,000-200,000 IU/m(2) ×3 per week), starting

SUBMITTER: Kennedy-Nasser AA 

PROVIDER: S-EPMC3989436 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Ultra low-dose IL-2 for GVHD prophylaxis after allogeneic hematopoietic stem cell transplantation mediates expansion of regulatory T cells without diminishing antiviral and antileukemic activity.

Kennedy-Nasser Alana A AA   Ku Stephanie S   Castillo-Caro Paul P   Hazrat Yasmin Y   Wu Meng-Fen MF   Liu Hao H   Melenhorst Jos J   Barrett A John AJ   Ito Sawa S   Foster Aaron A   Savoldo Barbara B   Yvon Eric E   Carrum George G   Ramos Carlos A CA   Krance Robert A RA   Leung Kathryn K   Heslop Helen E HE   Brenner Malcolm K MK   Bollard Catherine M CM  

Clinical cancer research : an official journal of the American Association for Cancer Research 20140226 8


<h4>Purpose</h4>GVHD after allogeneic hematopoietic stem cell transplantation (alloSCT) has been associated with low numbers of circulating CD4(+)CD25(+)FoxP3(+) regulatory T cells (Tregs). Because Tregs express high levels of the interleukin (IL)-2 receptor, they may selectively expand in vivo in response to doses of IL-2 insufficient to stimulate T effector T-cell populations, thereby preventing GVHD.<h4>Experimental design</h4>We prospectively evaluated the effects of ultra low-dose (ULD) IL-  ...[more]

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