Department of Oral Pathology and Oral Radiology, Institute of Dentistry and MediCity Research Laboratory, University of Turku, Turku, Finland.
Departments of Oral and Maxillofacial Diseases, Helsinki University and Helsinki University Central Hospital, Helsinki, Finland.
J Clin Virol. 2017 Dec;97:4-9. doi: 10.1016/j.jcv.2017.10.011. Epub 2017 Oct 23.
A persistent human papillomavirus (HPV) infection is a prerequisite for a HPV related cancer to develop. Asymptomatic, persistent HPV infections are not only found in genital tract, but also on oral mucosa. Oral HPV persistence may be associated with behavioural factors, but data on the role of innate immunity in oral HPV infections are still limited.
Salivary concentrations of matrix metalloproteinases MMP-8 and MMP-9, tissue inhibitor of MMPs (TIMP-1), myeloperoxidase, and serum concentrations of MMP-8 were analysed in women with a persistent oral HPV infection and, as a control, in women who remained HPV DNA-negative during a 6-year follow-up. The effects of smoking, lactation and alcohol use on the salivary and serum parameters were assessed, too.
A nested case-control setting was used to select a subgroup of 57 women with a persistent oral HPV infection and 102 controls from the Finnish Family HPV Study.
The salivary MMP-8/TIMP-1 molar ratio was lower in HPV DNA-positive women than in controls (p=0.036). The difference was more pronounced in non-smoking women, in this group also the salivary MMP-8 levels differed (p=0.047). There was a correlation between the salivary concentrations of myeloperoxidase and MMP-8 (r=0.567, p<0.001) or MMP-9 (r=0.234, p=003), but no correlation between salivary and serum MMP-8 levels. The MMP-9 concentration and the MMP-9/TIMP-1 molar ratio were significantly lower in smokers than in non-smokers (p=0.020 and p=0.003, respectively).
Persistent oral HPV infection was associated with a low salivary MMP-8 concentration indicating eventually a failure in oral anti-inflammatory defence.
持续性人乳头瘤病毒(HPV)感染是 HPV 相关癌症发展的前提。无症状、持续性 HPV 感染不仅存在于生殖道,也存在于口腔黏膜。口腔 HPV 持续性感染可能与行为因素有关,但关于固有免疫在口腔 HPV 感染中的作用的数据仍然有限。
分析持续性口腔 HPV 感染女性与 HPV DNA 持续阴性的女性(对照组)唾液中基质金属蛋白酶 MMP-8 和 MMP-9、组织抑制剂 MMPs(TIMP-1)、髓过氧化物酶以及血清中 MMP-8 的浓度。还评估了吸烟、哺乳和饮酒对唾液和血清参数的影响。
采用巢式病例对照设计,从芬兰 HPV 家庭研究中选择 57 例持续性口腔 HPV 感染女性和 102 例对照。
HPV DNA 阳性女性的唾液 MMP-8/TIMP-1 摩尔比低于对照组(p=0.036)。在不吸烟女性中差异更为明显,在此组中,唾液 MMP-8 水平也存在差异(p=0.047)。唾液髓过氧化物酶与 MMP-8(r=0.567,p<0.001)或 MMP-9(r=0.234,p=0.03)之间存在相关性,但唾液和血清 MMP-8 水平之间无相关性。与不吸烟者相比,吸烟者的 MMP-9 浓度和 MMP-9/TIMP-1 摩尔比显著降低(p=0.020 和 p=0.003)。
持续性口腔 HPV 感染与唾液 MMP-8 浓度降低相关,表明口腔抗炎防御可能失败。