Phenotypic alterations of dendritic cells are involved in suppressive activity of trichosanthin-induced CD8+CD28- regulatory T cells

Baolong Wang, Zhijun Jiao, Xiaoyi Shao, Liming Lu, Neng Yang, Xiaorong Zhou, Lijun Xin, Yun Zhou, Kuang Yen Chou

Research output: Contribution to journalArticlepeer-review

15 Scopus citations


The nature and differentiation of regulatory CD8+CD28 - T cells are poorly understood. In this study, we demonstrate that native Ag trichosanthin (Tk), a highly purified linear peptide isolated from a Chinese medicinal herb, is able to induce strong suppression of OVA-specific lymphoproliferation at low concentrations via activation of IL-4/IL-10-secreting CD8+CD28- regulatory T cells (Tregs). To elucidate the underlying mechanisms, we firstly identified two types of mouse inbred strains, high susceptible (HS) and low susceptible, for the Tk-related suppression. They are H-2d (or H-2b) and H-2k, respectively. The suppression is evoked only if bone marrow-derived dendritic cells (BDCs) instead of purified T cells are treated with Tk in an OVA-specific T-BDC interaction. Moreover, a special pattern of cytokine/transcription factors (IL-4 +IL-10+IFN-γ-Gata3+T-bet -) during suppressed OVA-specific T cell proliferation was observed in HS C57BL/6 but not in low-susceptible C3H/He mice. Consistently, the percentage of CD8+ CD28- Tregs preferentially expanded from 5.5 to 26.1% in the presence of Tk, an occurrence that was also detected only in HS C57BL/6 mice. These expanded Tregs were able to induce a strong inhibition of one-way MLCs, which indicated that the Tk-induced hyporeaction and the activation of CD8+CD28- Tregs might be under the influence of different genetic backgrounds. Additionally, obvious alterations of phenotypic parameters of BDCs after Tk stimulation were also identified, including enhanced production of IL-10, decreased secretion of IL-12, and detection of Jagged1, a Notch ligand on BDCs. Collectively, our data suggest that the changed APC-related factors are essential, at least in part, for the activation and differentiation of Tk-induced CD8+CD28- Tregs.

Original languageEnglish (US)
Pages (from-to)79-88
Number of pages10
JournalJournal of Immunology
Issue number1
StatePublished - Jul 1 2010

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


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