Logo image
Human memory CD4+T Cells Maintained in the Absence of Antigen Developed Regulatory T Cells Capable of Suppressing Antibody Responses
Abstract   Peer reviewed

Human memory CD4+T Cells Maintained in the Absence of Antigen Developed Regulatory T Cells Capable of Suppressing Antibody Responses

Adam McKinlay, K J Radford, D Gardiner, D Khalil, K Field, Fiona Burnell, D N J Hart and S Vuckovic
Tissue Antigens, Vol.66(5), pp.581-582
Annual Scientific Meeting of the Australasian Society for Immunology and 14th International HLA & Immunogenetics Workshop, 35th (Melbourne, Australia, 04-Dec-2005–08-Dec-2005)
2005
url
https://doi.org/10.1111/j.1399-0039.2005.00523.xView
Published Version

Abstract

Biochemistry and Cell Biology human memory CD4+T cells
Cytokines and antigen presenting cells (APC) maintain the mature T cell repertoire by homeostatic proliferation in the periphery. There are no conclusive data on the number and function of human memory CD4+T cells maintained in the periphery, in the absence of antigen, as a result of exposure to cytokines and access to blood APC. We showed that exposure to cytokines IL-7 and IL-15 and access to the MHC class II molecules on blood myeloid dendritic cells (MDC) allowed proliferation of memory CD4+T cells, which display a broad usage of the TCR V b repertoire. Memory CD4+T cells developed the capacity to suppress PWM-driven IgG and IgM antibody responses after exposure to IL-7 and IL-15 and independent of the access to blood MDC or Mo. The suppression of antibody responses by these memory CD4+T cells is dose-dependent: low numbers enhanced, whereas high numbers suppressed antibody responses. We conclude that IL-7, IL-15 and blood APC contribute to immunity by facilitating differentiation of regulatory memory CD4+T cells, which are capable of suppressing B cell differentiation and antibody production, as well as their role in controlling the number and effector function of memory CD4+T cells.

Details

Metrics

5 File views/ downloads
472 Record Views
Logo image