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Improper activation of the immune system contributes to a variety of clinical conditions, including autoimmune and allergic diseases as well as solid organ and bone marrow transplantation. One approach to counteract this activation is through adoptive therapy with regulatory T cells (Tregs). Efforts to manufacture these cells have led to good maunfacturing practice-compliant protocols, and Treg products are entering early clinical trials. Here, we report the stance of the European Union Cooperation in Science and Technology Action BM1305, "Action to Focus and Accelerate Cell-based Tolerance-inducing Therapies-A FACTT," which identifies hurdles hindering Treg clinical applications in Europe and provides possible solutions.

Original publication

DOI

10.1126/scitranslmed.aaa7721

Type

Journal article

Journal

Sci Transl Med

Publication Date

09/09/2015

Volume

7

Keywords

Clinical Trials as Topic, Drug Approval, Humans, Immunotherapy, T-Lymphocytes, Regulatory, Treatment Outcome