ORIGINAL RESEARCH article
Front. Immunol.
Sec. Immunological Tolerance and Regulation
Divergent CD27 expression marks the Treg induction trajectory
Chelsea Gootjes
Maurits G. Staal
Diahann T.S.L. Jansen
Antoinette M. Joosten
Jaap Jan Zwaginga
Bart O. Roep
Tatjana Nikolic
Department of Internal Medicine, Section Immunomodulation and Regenerative Cell Therapy, Leiden University Medical Center, Leiden, Netherlands
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Abstract
The induction of antigen-specific Tregs is explored as strategy to restore immune tolerance and halt progression of autoimmune diseases. However, the phenotypic changes in development of induced antigen specific Tregs in vivo have not been defined extensively. CD27 expression marks superior suppressive naturally occurring Tregs (nTregs) while in cancer, this showed to be a prognostic marker for tumor progression. Tumors indeed can promote the immunosuppressive effects of the CD27-CD70 co-stimulatory axis, and CD27 has been a target for immune checkpoint blockade in cancer. In this study, we explored changes in CD27 expression along with a panel of markers associated with immune regulation. For this, we induced Tregs in vitro from naive CD4 T cells by tolerogenic dendritic cells (tolDCs) and compared their phenotypes to effector T cells induced in parallel cultures by pro-inflammatory mDCs in time following priming. Clustering analysis revealed three clustering groups distinguishing induced Treg cultures from effector T cells, all marked by high CD27 expression, of which two clusters had a memory-like phenotype and expressed regulatory markers TIGIT, PD-1 and CD38. The kinetics of CD27 expression showed that naive T cells increase CD27 expression during their differentiation into memory-like Tregs, whereas CD27 is lost during differentiation into pro-inflammatory effector T cells. Furthermore, the presence of CD27 and TIGIT-expressing memory-like Tregs positively correlated with the inhibition capacity of the induced Treg lines in vitro. Increased ratios of these Tregs over effector T cells in vivo following vaccination of T1D patients with tolerogenic DCs pulsed with islet autoantigen correlated with increased islet-specific immune regulation ex vivo. Our results define a population of induced Tregs in vitro and in vivo that is marked by elevated CD27 expression. Hence, CD27 expression may be useful to monitor therapeutic efficacy of Treg induction in vivo in clinical trials.
Summary
Keywords
CD27, Immunotherapy, induced Tregs, Tolerance induction, Treg development
Received
28 November 2025
Accepted
16 February 2026
Copyright
© 2026 Gootjes, Staal, Jansen, Joosten, Zwaginga, Roep and Nikolic. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Chelsea Gootjes; Tatjana Nikolic
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