Go to JCI Insight
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
  • Clinical Research and Public Health
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Gastroenterology
    • Immunology
    • Metabolism
    • Nephrology
    • Neuroscience
    • Oncology
    • Pulmonology
    • Vascular biology
    • All ...
  • Videos
    • Conversations with Giants in Medicine
    • Video Abstracts
  • Reviews
    • View all reviews ...
    • Complement Biology and Therapeutics (May 2025)
    • Evolving insights into MASLD and MASH pathogenesis and treatment (Apr 2025)
    • Microbiome in Health and Disease (Feb 2025)
    • Substance Use Disorders (Oct 2024)
    • Clonal Hematopoiesis (Oct 2024)
    • Sex Differences in Medicine (Sep 2024)
    • Vascular Malformations (Apr 2024)
    • View all review series ...
  • Viewpoint
  • Collections
    • In-Press Preview
    • Clinical Research and Public Health
    • Research Letters
    • Letters to the Editor
    • Editorials
    • Commentaries
    • Editor's notes
    • Reviews
    • Viewpoints
    • 100th anniversary
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • Reviews
  • Review series
  • Conversations with Giants in Medicine
  • Video Abstracts
  • In-Press Preview
  • Clinical Research and Public Health
  • Research Letters
  • Letters to the Editor
  • Editorials
  • Commentaries
  • Editor's notes
  • Reviews
  • Viewpoints
  • 100th anniversary
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
CD4+CD25+ regulatory T cells suppress allograft rejection mediated by memory CD8+ T cells via a CD30-dependent mechanism
Zhenhua Dai, … , George Tellides, Fadi G. Lakkis
Zhenhua Dai, … , George Tellides, Fadi G. Lakkis
Published January 15, 2004
Citation Information: J Clin Invest. 2004;113(2):310-317. https://doi.org/10.1172/JCI19727.
View: Text | PDF
Article

CD4+CD25+ regulatory T cells suppress allograft rejection mediated by memory CD8+ T cells via a CD30-dependent mechanism

  • Text
  • PDF
Abstract

CD4+CD25+ regulatory T (Treg) cells suppress naive T cell responses, prevent autoimmunity, and delay allograft rejection. It is not known, however, whether Treg cells suppress allograft rejection mediated by memory T cells, as the latter mount faster and stronger immune responses than their naive counterparts. Here we show that antigen-induced, but not naive, Treg cells suppress allograft rejection mediated by memory CD8+ T cells. Suppression was allospecific, as Treg cells induced by third-party antigens did not delay allograft rejection. In vivo and in vitro analyses revealed that the apoptosis of allospecific memory CD8+ T cells is significantly increased in the presence of antigen-induced Treg cells, while their proliferation remains unaffected. Importantly, neither suppression of allograft rejection nor enhanced apoptosis of memory CD8+ T cells was observed when Treg cells lacked CD30 or when CD30 ligand–CD30 interaction was blocked with anti–CD30 ligand Ab. This study therefore provides direct evidence that pathogenic memory T cells are amenable to suppression in an antigen-specific manner and identifies CD30 as a molecule that is critical for the regulation of memory T cell responses.

Authors

Zhenhua Dai, Qi Li, Yinong Wang, Ge Gao, Lonnette S. Diggs, George Tellides, Fadi G. Lakkis

×

Figure 5

Options: View larger image (or click on image) Download as PowerPoint
Treg cells promote the apoptosis of memory CD8+ T cells in vitro in a co...
Treg cells promote the apoptosis of memory CD8+ T cells in vitro in a contact-dependent manner. (a) Purified memory CD8+ T cells (CD8+CD44high) were cultured with Treg cells at a ratio of 1:2 (Treg/M) in 24-well plates in the presence of irradiated BALB/c spleen cells (APCs) for 48 hours. Intracellular expression of IFN-γ is shown in histograms after gating on CD8+CD44high cells. The shaded histogram shows isotype control, and the dotted, gray, and black lines represent memory cells (M) alone, M plus naive Treg cells, and M plus DST Treg cells, respectively. (b) Memory CD8+ T cells were incubated as described above. Their proliferation was measured by [3H]-TdR uptakes. Results are presented as the mean of triplicate cultures. (c) Memory CD8+ T cells were cultured with Treg cells (1:2, Treg/memory) in 24-well plates and transwell in the presence of APCs and the indicated agents (5 μg/ml anti-FasL) for 48 hours. Cells were then stained for surface markers, fixed, permeabilized, and measured for apoptosis by the TUNEL method. One of three experiments is presented; data are expressed as percentage of apoptotic CD8+CD44high cells.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

Sign up for email alerts