Therapeutic potential of low-dose IL-2 in a chronic GVHD patient by in vivo expansion of regulatory T cells.

Cytokine

The Institute for Translational Research and Molecular Imaging, The Catholic University of Korea College of Medicine, Seoul, Republic of Korea; Laboratory of Immune Regulation, Convergent Research Consortium for Immunologic Disease, Seoul, Republic of Korea; The Catholic Blood and Marrow Transplantation Center, Seoul St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Republic of Korea. Electronic address:

Published: February 2016

AI Article Synopsis

  • cGVHD is a common complication after allogeneic HSCT, marked by autoimmune-like inflammation and lower Treg levels.
  • Recent studies suggest that low-dose IL-2 can boost Treg levels, aiding in immune regulation and improving symptoms in cGVHD patients.
  • A case study showed that low-dose IL-2 therapy led to significant Treg expansion and some clinical benefits, indicating that while promising, more targeted strategies may be necessary for lasting therapeutic effects.

Article Abstract

Chronic graft-versus-host disease (cGVHD) is a common complication following allogeneic hematopoietic stem cell transplantation (HSCT), which is characterized by autoimmune like inflammatory responses and reduced levels of regulatory T cells (Tregs). Recently, the use of low-dose IL-2 has been reported to selectively increase Tregs and therefore facilitate immune regulation and promote clinical improvements in cGVHD patients. In this report, we describe the case of a cGVHD patient who was treated with daily low-dose IL-2 therapy. Our observations demonstrate that low-dose IL-2 could induce significant expansion of Tregs in vivo leading to improved Treg/Th17 ratios. The patient showed moderate clinical benefits suggesting that multiple factors may be involved in the immunological responses. Therefore, while the therapeutic potential of low-dose IL-2 is promising, strategic approaches may be needed to induce a clinically significant and sustained Treg effect.

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http://dx.doi.org/10.1016/j.cyto.2015.11.020DOI Listing

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