Usage of Murine T-cell Hybridoma Cells as Responder Cells Reveals Interference of with Human Dendritic Cell-mediated Antigen Presentation.

Direct effects of on human CD4 T-cells hamper disentangling a possible bacterial-mediated interference with major histocompatibility complex class II (MHC-II)-dependent antigen presentation to these cells. To overcome this limitation, we employed a previously described assay, which enables assessing human antigen-processing cell function by using murine T-cell hybridoma cells restricted by human leukocyte antigen (HLA) alleles. HLA-DR1 monocyte-derived dendritic cells were exposed to and pulsed with the antigen 85B from . Interleukin-2 (IL-2) secretion by AG85B-specific hybridoma cells was then evaluated as an integral reporter of cognate antigen presentation. This methodology enabled revealing of interference of with the antigen-presenting capacity of human dendritic cells.