The Specific Regulation Of Immune Responses By CD8+T Cells Restricted By The MHC Class Ib Molecule, Qa-1

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Abstract
Over the last three decades considerable evidence has accumulated that CD8+T cells regulate peripheral immune responses, in part, by specifically controlling the outgrowth of antigen-triggered CD4+T cells. This regulatory function of CD8+T cells has been shown, in vivo, to control the emergence of autoreactive CD4+T cells as well as CD4+T cells reactive to conventional antigens, including alloantigens. In this review, we summarize the evidence that this immune suppression mediated by CD8+T cells is dependent, in part, on specific cognate interactions between MHC class I–restricted regulatory CD8+cells and antigen-activated CD4+T cells. Moreover, we review the evidence that regulatory CD8+T cells recognize antigen-activated CD4+T cells in a TCR specific manner restricted by the MHC class Ib molecule, Qa-1. The Qa-1 molecule may be uniquely qualified to serve this MHC restrictive function because, unlike conventional MHC molecules, it is preferentially and transiently expressed on activated and not resting CD4+T cells. This may assure that only recently antigen-activated CD4+T cells expressing Qa-1/TCR peptide complexes will induce regulatory CD8+T cells and subsequently become susceptible to regulation. Because Qa-1 also binds to self Qdm peptides that trigger NK (CD94/ NKG2) receptors on CD8+T cells, the machinery for homeostatic regulation of regulatory CD8+T cells can be envisioned. Finally, we propose a model by which these TCR specific, Qa-1-restricted regulatory CD8+T cells selectively downregulate antigen-activated T cells expressing TCRs of certain affinities. Ultimately these regulatory CD8+T cells control the peripheral TCR repertoire during the course of immune responses to both self and foreign antigens.