To verify the response of host cells to trichomonad infection, a primary culture of bovine epithelial cells (BOECs) was grown to model host cells, following previously published procedures (Midlej et al. 2009). The JT strain of T. vaginalis (Fig. 1A) and the K strain of T. foetus (Fig. 1B) were used as models for human and bovine parasites, respectively. Parasites were cultivated in trypticaseyeast extract-maltose (TYM) medium (Diamond 1957) Financial support: CNPq, FAPERJ, CAPES, PRONEX, AUSU + Corresponding author: marlenebenchimol@gmail.com Received 28 January 2012 Accepted 18 July 2012 supplemented with 10% foetal bovine serum. Host cell cultures were exposed to a parasite:BOECS cell ratio of 5:1 for 12 h in 37ºC (Fig. 1C, D). Cells were equilibrated in incubation medium for 5 min at 37ºC (5% CO 2 ) prior to parasite addition. The medium contained two parts of complete DMEM (pH 7.2) and one part TYM medium (W/D 2:1) without serum. The incubation medium and temperature were chosen after testing parasite and host cell viabilities in several different conditions. The supernatants of cultures with parasites or without (controls) were collected and cytokine levels were quantified with specific kits for measuring