Leclair Catherine M L, Leeborg Nicky J, Jacobson-Dunlop Erick, Goetsch Martha F, Morgan Terry K
Departments of 1Obstetrics and Gynecology and 2Pathology, Oregon Health & Science University, Portland, OR.
J Low Genit Tract Dis. 2014 Apr;18(2):195-201. doi: 10.1097/LGT.0b013e3182a55591.
To better understand the potential disease triggers of neurogenic inflammation in provoked localized vulvodynia (PLV), our objective was to determine whether the types of infiltrating lymphocytes were different in vestibular biopsies from women with primary PLV, secondary PLV, and unaffected controls.
Secondary retrospective analysis of archived vestibular biopsies from a series of adult premenopausal women with primary PLV (n = 10), secondary PLV (n = 10), and unaffected controls (n = 4) was performed. All study patients had severe entry dyspareunia for more than 1 year. Subjects were excluded if pregnant, or they had a known infection, or history of generalized vulvodynia. Biopsies were performed during the midfollicular phase. Lymphocyte subtypes were highlighted in histologic sections using antibodies against CD3, CD4, and CD8 and scored as the mean number of T-cell subtypes per high-power field. Flow cytometry was also used to test fresh biopsies from a de novo prospective series of primary PLV (n = 4) and unaffected controls (n = 2).
Unaffected control biopsies showed more CD8-positive than CD4-positive T cells, similar to previous reports of the gynecologic tract. In contrast, biopsies from women with primary PLV showed significantly more CD4-positive T cells than those from women with secondary PLV and unaffected controls (p = .003). This observation was further supported by flow cytometry.
CD4-positive T cells are more numerous in vestibular biopsies from premenopausal women with primary PLV. This may be important because subtypes of CD4-positive T cells are specifically recruited by infectious, allergic, or autoimmune triggers. Future studies distinguishing these subtypes may lead to new insights into this common disease.
为了更好地了解激发性局限性外阴痛(PLV)中神经源性炎症的潜在疾病触发因素,我们的目的是确定原发性PLV、继发性PLV女性以及未受影响的对照组女性的前庭活检中浸润淋巴细胞的类型是否不同。
对一系列患有原发性PLV(n = 10)、继发性PLV(n = 10)和未受影响的对照组(n = 4)的成年绝经前女性的存档前庭活检进行二次回顾性分析。所有研究患者均有严重的性交时阴道口疼痛超过1年。如果患者怀孕、有已知感染或全身性外阴痛病史,则将其排除。活检在卵泡中期进行。使用抗CD3、CD4和CD8的抗体在组织学切片中突出显示淋巴细胞亚型,并将其计为每个高倍视野中T细胞亚型的平均数。还使用流式细胞术对一组新的原发性PLV(n = 4)和未受影响的对照组(n = 2)的新鲜活检进行检测。
未受影响的对照组活检显示CD8阳性T细胞比CD4阳性T细胞更多,这与先前关于生殖道的报道相似。相比之下,原发性PLV女性的活检显示CD4阳性T细胞明显多于继发性PLV女性和未受影响的对照组(p = 0.003)。流式细胞术进一步支持了这一观察结果。
在患有原发性PLV的绝经前女性的前庭活检中,CD4阳性T细胞数量更多。这可能很重要,因为CD4阳性T细胞亚型是由感染、过敏或自身免疫触发因素特异性募集的。区分这些亚型的未来研究可能会为这种常见疾病带来新的见解。