T Suppressor Lymphocytes Inhibit NF-κB-Mediated Transcription of CD86 Gene in APC
Open Access
- 15 December 1999
- journal article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 163 (12) , 6386-6392
- https://doi.org/10.4049/jimmunol.163.12.6386
Abstract
CD8+CD28− human T suppressor cells (Ts) act on APC, inhibiting their ability to elicit Th activation and proliferation. This effect is due to inhibition of the CD40 pathway which normally leads to CD80 and CD86 up-regulation. To determine whether Ts inhibit expression of B7 molecules by blocking transcription, we cloned and characterized the CD86 promoter. Mutational analysis revealed that Ts inhibit transcription driven by the CD86 promoter. The NF-κB binding site, at −612 of the CD86 promoter, is essential for Th-induced transcription. In cultures containing Th and Ts, Ts inhibit Th-induced NF-κB activation in APC. Together, these findings indicate that Ts inhibition of NF-κB activation in APC is a means by which they regulate the activation and proliferation of Th.Keywords
This publication has 22 references indexed in Scilit:
- A cell type-specific enhancer in the human B7.1 gene regulated by NF-kappaB.The Journal of Experimental Medicine, 1996
- Genomic organization of the gene coding for the costimulatory human B-lymphocyte antigen B7-2 (CD86)Immunogenetics, 1995
- Induction of the transcription factors NF-?B, AP-1 and NF-AT during B cell stimulation through the CD40 receptorInternational Immunology, 1995
- In vitro induction of T cell anergy by blocking B7 and early T cell costimulatory molecule ETC-1/B7-2Immunity, 1994
- How B and T cells talk to each otherNature, 1994
- CD40 expression by human monocytes: regulation by cytokines and activation of monocytes by the ligand for CD40.The Journal of Experimental Medicine, 1993
- Human T-cell clonal anergy is induced by antigen presentation in the absence of B7 costimulation.Proceedings of the National Academy of Sciences, 1993
- Activated T cells induce expression of B7/BB1 on normal or leukemic B cells through a CD40-dependent signal.The Journal of Experimental Medicine, 1993
- Costimulation of T lymphocytes: the role of CD28, CTLA-4, and B7/BB1 in interleukin-2 production and immunotherapyCell, 1992
- A 39-kDa protein on activated helper T cells binds CD40 and transduces the signal for cognate activation of B cells.Proceedings of the National Academy of Sciences, 1992