The Dynamic Process of Vaginal Microbiota and Mucosal Immunity After Focused Ultrasound Treatment of Cervical Intraepithelial Neoplasia Patients With Fertility Requirement
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Cytology
研究概览
简要总结
Cervical cancer is the fourth leading cause of cancer death in women worldwide, and cervical intraepithelial neoplasia (CIN) can progress to cervical cancer. Therefore, timely treatment of CIN is critical in preventing the occurrence of cervical cancer. With the implementation and promotion of the World Health Organization's 2030 Global Strategy for the Elimination of Cervical Cancer, an increasing number of women are detecting and treating CIN at an earlier stage. Common treatment methods include ablation treatment and excision treatment, but for women who are planning to have children, the risk of cervical insufficiency and pregnancy complications is greatly increased after excisional treatment, so ablation treatment seems to be a better choice.
详细描述
Focused ultrasound (FUS) is a new ablation method for the treatment of CIN that has received a lot of attention because of its unique ablation mode (from inside to outside) and lack of smoke, ionizing radiation, and other side effects. Preliminary studies have found that FUS treatment is safe and effective at reversing CIN, with curative effects comparable to traditional ablation and excisional treatments. However, few studies have reported the mechanism of FUS in the treatment of CIN. As a kind of ablation treatment, it is unclear whether FUS, like other ablation treatment mechanisms, stimulates the immune response of the body to promote the reversal of the lesions by in situ necrotic lesions.
There is limited evidence to support the link between FUS, immune response, and CIN. Fu compared the cervical tissues of patients with CIN before and after FUS treatment and found that the expression of p16 and ki-67 decreased while the expression of Fas increased after treatment, indicating that FUS can regulate cell proliferation and apoptosis-related proteins, and promote the recovery of cervical tissues. More recently, Zeng compared the cervical immune microenvironment in patients with CIN before and after FUS treatment. It has shown that FUS treatment increased the expression of ERAP1 in cervical tissue and decreased the level of IgA and IL-10 in cervicovaginal lavage, which indicated that FUS treatment can regulate the cervical immune microenvironment.
The immune response of the body is a dynamic and changing process. Any attempt to infer further on immunological changes before and after treatment require dynamic studies that will explore how FUS ablation of the disease, i.e. CIN, will alter the cervical immune microenvironment. The local immunological indexes produced by FUS treatment of CIN should be a dynamic process, and more time points should be selected to monitor the changes in these immunological indexes. Currently, there are no such studies.
At the same time, a large number of studies suggest that Vaginal Microbiota(VMB) can alter the cervicovaginal immune microenvironment and Lactobacillus spp. depleted and high diversity of VMB is prone to form a pro-inflammatory environment, which in turn promotes the progression of CIN and the occurrence of cervical cancer. Therefore, to further explore the mechanisms of FUS ablation treatment of CIN and clearance of HPV, this interventional study was conducted to dynamically observe the changes in the VMB and mucosal immunity in patients with CIN before and after FUS ablation treatment and to compare with untreated healthy controls. This may also have implications for the persistence and recurrence of lesions.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 60 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •patients aged 18-60 years old;
- •patients who had sexual life;
- •patients who had HPV infection;
- •patients who apply to ablation therapy
- •pathological report indicates CIN
排除标准
- •pregnant or lactating women;
- •patients who had cervical treatment ;
- •patients who had genital tract infection ;
- •patients who had chronic diseases, such as allergic diseases ,autoimmune diseases and so on;
- •patients who received antibiotics or pessaries within 14 days of sampling.
结局指标
主要结局
Cytology
时间窗: We will get specimens before therapeutic day, after treatment 84-112 days and 168-196 days respectively.
Thinprep cytologic test
Immunological indexes
时间窗: We will get specimens in therapeutic day, after treatment 7-10 days,84-112days and 168-196 days respectively.
Immunological indexes(IFN-γ、IL-8、IL-10、IL-1β、SIgA) in cervical secretions will be measured by enzyme-linked immunosorbent assay (ELISA).
Anti-microbial peptides
时间窗: We will get specimens in therapeutic day, after treatment 7-10 days,84-112 days and 168-196 days respectively.
Anti-microbial peptides levels (hBD-1、SLPI ) in cervical secretions will be measured by enzyme-linked immunosorbent assay (ELISA).
Vaginal microbiota
时间窗: We will get specimens before therapeutic day, after treatment 84-112 days and 168-196 days respectively.
We will evaluate vaginal microbiota by bacterial diversity and richness, and Lactobacillus grading.
HPV genotyping
时间窗: We will get specimens before therapeutic day, after 84-112 days and 168-196 days respectively.
HPV DNA testing and genotyping
次要结局
- Antisperm antibody(We will get specimens before therapeutic day, after treatment 84-112 days and 168-196 days respectively.)
- Measurement of dimensions of cervix(We will measure the dimensions of cervix before therapeutic day and after treatment 84-112 days respectively.)
研究者
Shufang Chang
professor
The Second Affiliated Hospital of Chongqing Medical University
