The Transcription Factor Hobit Identifies Human Cytotoxic CD4 T Cells.

The T cell lineage is commonly divided into CD4-expressing helper T cells that polarize immune responses through cytokine secretion and CD8-expressing cytotoxic T cells that eliminate infected target cells by virtue of the release of cytotoxic molecules. Recently, a population of CD4 T cells that conforms to the phenotype of cytotoxic CD8 T cells has received increased recognition. These cytotoxic CD4 T cells display constitutive expression of granzyme B and perforin at the protein level and mediate HLA class II-dependent killing of target cells. In humans, this cytotoxic profile is found within the human cytomegalovirus (hCMV)-specific, but not within the influenza- or Epstein-Barr virus-specific CD4 T cell populations, suggesting that, in particular, hCMV infection induces the formation of cytotoxic CD4 T cells. We have previously described that the transcription factor Homolog of Blimp-1 in T cells (Hobit) is specifically upregulated in CD45RA effector CD8 T cells that arise after hCMV infection. Here, we describe the expression pattern of Hobit in human CD4 T cells. We found Hobit expression in cytotoxic CD4 T cells and accumulation of Hobit CD4 T cells after primary hCMV infection. The Hobit CD4 T cells displayed highly overlapping characteristics with Hobit CD8 T cells, including the expression of cytotoxic molecules, T-bet, and CX3CR1. Interestingly, γδ T cells that arise after hCMV infection also upregulate Hobit expression and display a similar effector phenotype as cytotoxic CD4 and CD8 T cells. These findings suggest a shared differentiation pathway in CD4, CD8, and γδ T cells that may involve Hobit-driven acquisition of long-lived cytotoxic effector function.