To further characterize the intracellular mechanisms induced by VLPs, we will investigate the role of MAP kinases that have been implicated in NK-cell degranulation or in ADCC after CD16 triggering 43, 44. Overall, our results show that NK cells could participate in the high rate of spontaneous regression of HPV-associated preneoplastic lesions. Indeed, HPV infections

are cleared in ∼90% of women within 2 years 8. NK cells present in these preneoplastic lesions could be activated by L1 viral particles and kill HPV-infected cells. Alternatively, NK cells could help to induce an adaptive immune response SRT1720 against HPV by secreting cytokines. The presence of L1 seems to be important for dysplasia regression since this phenomenon has been correlated to L1 protein expression 45. Moreover, E7 protein from

high-risk HPVs has been shown to reduce cell surface expression of MHC Class I molecules 46, rendering these cells susceptible to lysis by NK cells. However, viruses have developed mechanisms to avoid the immune response and some of these mechanisms are directed against NK cells. For example, direct infection of NK cells by vaccinia virus has been shown to negatively modulate NK-cell function 47 and internalization of influenza virions in NK cells has also been described to cause a decrease in NK cytotoxicity 48. In patients with invasive cervical cancer, NK cells express a lower level of NKp30, NKp46 and NKG2D and have a lower

capacity to Selleckchem Metabolism inhibitor kill tumor cells compared with NK cells from healthy donors 49, suggesting that the immune escape mechanisms against NK cells occur in late-stage HPV-associated lesions. A better understanding of the role of NK cells in HPV-associated lesions could help to design more effective vaccines and treatment strategies for this disease. CasKi and NK92 cell lines were obtained from ATCC. NK92 cells were transduced with lentiviral vectors coding for CD16, as previously described 50. In order to increase the level of CD16 expression, NK92 cells expressing a high level Oxalosuccinic acid of CD16 were sorted by flow cytometry. NK92 CD16+ and parental cell lines were grown in RPMI 1640 medium (GIBCO, Merelbeke, Belgium) supplemented with 8% human serum (centre de transfusion sanguine, Centre Hospitalier Universitaire, Liège, Belgium) and 100 IU/ml of IL-2 (Proleukine, Novartis, Vilvoorde, Belgium). Human and bovine sera used in this study did not contain anti-L1 HPV16 antibodies detected with a specific ELISA 51. Primary NK cells were isolated by negative magnetic selection (EasySep® Human NK Cell Enrichment Kit, STEMCELL technologies, Grenoble, France) from peripheral blood mononuclear cells (PBMCs) obtained from buffy coats of healthy donors. The purity of NK cells was assessed by flow cytometry and the percentage of NK cells (CD56+CD16+CD3−) was >95%.