| Literature DB >> 25913194 |
Dominik Wolf1,2, Sieghart Sopper2,3, Andreas Pircher2, Guenther Gastl2, Anna Maria Wolf1,2.
Abstract
Immune escape is a hallmark of cancer. Regulatory T cells (Treg) have been described to maintain peripheral tolerance. The role of Treg in cancer is ambiguous, as they are central inhibitory regulators in solid tumors, whereas during inflammation-driven tumorigenesis they prevent cancer initiation by restraining inflammation. As a consequence, under conditions with chronic inflammation that may initiate malignant transformation, application rather than depletion of Treg may be helpful. In solid tumors, however, the success story of immune-activating antibodies targeting checkpoint molecules of T cell activation fuels the hope that Treg inactivation or depletion may additionally boost anti-tumor immune response. In this review we summarize important aspects on the dual role of Treg in cancer to provide a rationale for future Treg targeting attempts.Entities:
Mesh:
Year: 2015 PMID: 25913194 DOI: 10.1002/jcp.25016
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384