Definition of the mitogenic factor (MF) as a novel streptococcal superantigen that is different from streptococcal pyrogenic exotoxins A, B, and C

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Abstract
Human T cell activation by recombinant mitogenic factor (rMF) was investigated in comparison with that by recombinant streptococcal pyrogenic exotoxins (rSPE) A, B, and C. Recombinant MF, rSPEA, and rSPEC were mitogenic for peripheral blood mononuclear cells (PBMC), whereas rSPEB was not. Recombinant MF required only HLA‐DR for the stimulation of PBMC, as determined using monoclonal antibodies (mAb) to HLA class II molecules and the mouse L cells transfected with HLA class II molecules. Recombinant SPEA and rSPEC required HLA‐DR or HLA‐DQ molecule. Recombinant MF selectively stimulated Vβ2, Vβ7, Vβ8, Vβ18 and Vβ21‐bearing T cells, whereas rSPEA and rSPEC activated Vβ2 and Vβ6‐bearing T cells as evaluated by the quantitative T cell receptor (TCR) analytical method. No clonality was observed in the nucleotide sequences of complementarity determining region 3 of TCR Vβ in T cells responding to rMF. The profiles of cytokine production by PBMC in response to rMF, rSPEA, and rSPEC were quite similar. In summary, these results demonstrate that both HLA class II molecules and the TCR Vβ required for rMF‐mediated T cell activation are distinct from those required for rSPEA or rSPEC‐mediated activation. Therefore, the MF is a novel streptococcal superantigen which is different from SPEA, SPEB, and SPEC.