Macrophages are essential cells of the innate immune response against microbial infections, and they have the ability to adapt under both pro-and anti-inflammatory conditions and develop different functions. A growing body of evidence regarding a novel macrophage subpopulation that expresses CD3 has recently emerged. Here, we explain that human circulating monocytes can be differentiated into CD3 + TCRαβ + and CD3 + TCRαβ − macrophages. Both cell subpopulations express on their cell surface HLA family molecules, but only the CD3 + TCRαβ + macrophage subpopulation co-express CD1 family molecules and transmembrane TNF (tmTNF). CD3 + TCRαβ + macrophages secrete IL-1β, IL-6 IP-10, and MCP-1 by both tmTNF-and CD3-dependent pathways, while CD3 + TCRαβ − macrophages specifically produce IFN-γ, TNF, and MIP-1β by a CD3-dependent pathway. In this study, we also used a mouse model of BCG-induced pleurisy and demonstrated that CD3 + myeloid cells (TCRαβ + and TCRαβ − cells) are increased at the infection sites during the acute phase (2 weeks post-infection). Interestingly, cell increment was mediated by tmTNF, and the soluble form of TNF was dispensable. BCG-infection also induced the expression of TNF receptor 2 on CD3 + myeloid cells, which increased after BCG-infection, suggesting that the tmTNF/TNFRs axis plays an important role in the presence or function of these cells in tuberculosis.