Differential susceptibility of human T(h)1 versus T(h)2 cells to induction of anergy and apoptosis by ECDI/antigen-coupled antigen-presenting cells

Arthur A. Vandenbark*, David Barnes, Tom Finn, Dennis N. Bourdette, Ruth Whitham, Ian Robey, Johnan Kaleeba, Bruce F. Bebo, Steven D. Miller, Halina Offner, Yuan K. Chou

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

27 Scopus citations


Antigen-coupled antigen-presenting cells (APC) serve as potent tolerogens for inhibiting immune responses in vivo and in vitro, apparently by providing an antigen-specific signal through the TCR in the absence of co-stimulation. Although this approach has been well studied in rodents, little is known about its effects on human T cells. We evaluated the specificity and mechanisms of tolerization of human T cells in vitro using monocyte-enriched adherent cells that were pulsed with antigen and treated with the cross-linker, 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide (ECDI). Autologous antigen-coupled APC selectively tolerized T cells of the T(h)1 but not T(h)2 lineage through a mechanism that involved both antigen-specific and antigen-non-specific elements. The tolerization process was dependent on the ECDI and antigen concentration, and the coupling time, and was reflected by initial up-regulation of CD25. However, upon re-stimulation with fresh APC and antigen, tolerized T(h)1 cells failed to proliferate or to produce T(h)1 cytokine message or secreted protein, had decreased expression of CD25, CD28 and B7 and increased expression of MHC class II molecules, and demonstrated an enhanced commitment to apoptosis. T(h)1 cell tolerization could be prevented by adding anti-CD28 antibody, IL-2 or untreated APC at the same time as the ECDI/antigen-coupled APC, or reversed by adding anti-CD28 antibody or IL-2 upon re-stimulation with fresh APC plus antigen. Thus, the tolerizing effect of ECDI/antigen-coupled APC on human T(h)1 cells appears to involve a reversible anergy mechanism leading to apoptosis, whereby the targeted T cells receive full or partial activation through the TCR, without coordinate co-stimulation. These data suggest dichotomous signaling requirements for inactivating cells of the T(h)1 and T(h)2 lineages that may have important implications for treatment of T(h)1-mediated autoimmune or inflammatory diseases.

Original languageEnglish (US)
Pages (from-to)57-66
Number of pages10
JournalInternational Immunology
Issue number1
StatePublished - 2000


  • Altered antigen-presenting cells
  • Human T cells
  • Tolerance induction

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


Dive into the research topics of 'Differential susceptibility of human T(h)1 versus T(h)2 cells to induction of anergy and apoptosis by ECDI/antigen-coupled antigen-presenting cells'. Together they form a unique fingerprint.

Cite this