Bais Aagje G, Beckmann Ilse, Ewing Patricia C, Eijkemans Marinus J C, Meijer Chris J L M, Snijders Peter J F, Helmerhorst Theo J M
Department of Obstetrics and Gynaecology, Erasmus University Medical Center, 3000 CA, Rotterdam, The Netherlands.
Mediators Inflamm. 2007;2007:24147. doi: 10.1155/2007/24147.
We investigated the effect of HR-HPV infection on the capacity of the cytokine network in whole blood cultures during carcinogenesis of cervical carcinoma.
Thirty-nine women with moderate dysplasia, severe dysplasia, cervical carcinoma, or without dysplasia formed the study group. The control group consisted of 10 HR-HPV-negative women without CIN. Whole blood cultures were stimulated with phytohemagglutinin (PHA) and concentrations of tumour necrosis factor alpha (TNFalpha), interferon gamma (IFNgamma), interleukin 2 (IL-2), interleukin 12 (IL-12), interleukin 4 (IL-4), and interleukin 10 (IL-10) were determined by ELISAs.
A significant increase in cytokine release was detected in HR-HPV-positive women without dysplasia. In women with cervical cancer, release of IFNgamma and IL-12 was of the same magnitude as in HR-HPV-positive women without clinical manifestations. Most Th1-type/Th2-type ratios decreased form CIN II to CIN III, and increased from CIN III to invasive carcinoma.
(1) Infection with HR-HPV without expression of cervical dysplasia induces activation of the cytokine network. (2) Increases in ratios of Th1-type to Th2-type cytokines at the stage of cervical carcinoma were found by comparison with stage CIN III. (3) Significant changes in the kinetics of cytokine release to a Th2-type immune response in blood of women with cervical dysplasia occurred progressively from CIN II to CIN III.
我们研究了高危型人乳头瘤病毒(HR-HPV)感染对宫颈癌发生过程中全血培养物中细胞因子网络功能的影响。
39名患有中度发育异常、重度发育异常、宫颈癌或无发育异常的女性组成研究组。对照组由10名无宫颈上皮内瘤变(CIN)的HR-HPV阴性女性组成。用植物血凝素(PHA)刺激全血培养物,并用酶联免疫吸附测定法(ELISA)测定肿瘤坏死因子α(TNFα)、干扰素γ(IFNγ)、白细胞介素2(IL-2)、白细胞介素12(IL-12)、白细胞介素4(IL-4)和白细胞介素10(IL-10)的浓度。
在无发育异常的HR-HPV阳性女性中检测到细胞因子释放显著增加。在宫颈癌女性中,IFNγ和IL-12的释放水平与无临床表现的HR-HPV阳性女性相同。从CIN II到CIN III,大多数Th1型/Th2型细胞因子比值下降,而从CIN III到浸润癌则升高。
(1)无宫颈发育异常表现的HR-HPV感染可诱导细胞因子网络激活。(2)与CIN III期相比,在宫颈癌阶段发现Th1型细胞因子与Th2型细胞因子的比值增加。(3)从CIN II到CIN III,宫颈发育异常女性血液中细胞因子释放动力学向Th2型免疫反应发生了显著变化。