Li Xin-Yi, Duan Hong-Ji, Liu Xiang-Yuan, Deng Xiao-Li
Department of Rheumatology and Immunology, Peking University Third Hospital, Haidian District, Beijing 100191, China.
Chin Med J (Engl). 2020 Oct 5;133(19):2287-2294. doi: 10.1097/CM9.0000000000000948.
B-cell activating factor (BAFF) is vital for B cell survival. Serum BAFF levels are elevated in thrombotic antiphospholipid syndrome, but little is known about levels in patients with positive antiphospholipid antibodies (aPLs) and previous adverse pregnancy outcomes (APOs). We aimed to analyze serum BAFF concentrations of these patients in early pregnancy along with different pregnancy outcomes.
Thirty-six pregnant patients positive for aPLs and previous APOs (patient group), 25 healthy pregnant females (HP group) and 35 healthy non-pregnant females (HNP group) from the Peking University Third Hospital, between October 2018 and March 2019, were enrolled in this study. Serum of HNP and serum of patients as well as HP in the first gestational trimester were collected. Enzyme-linked immunosorbent assay kits were used to measure serum BAFF and interferon-alpha (IFN-α) concentrations. Cytometric bead array analysis was used to measure serum concentrations of cytokines. The patient group was further divided into APOs and non-APOs (NAPOs) group, fetal loss and live birth group according to pregnancy outcomes. The Mann-Whitney U-test was used to assess significance between and within groups. Spearman rank-order was used to evaluate correlation coefficients between BAFF and related cytokines.
The serum BAFF level in HP group was significantly lower than HNP group (245.24 [218.80, 265.90] vs. 326.94 [267.31, 414.80] pg/mL, Z = -3.966, P < 0.001). The BAFF level was obviously elevated in patient group compared to that in HP group (307.77 [219.86, 415.65] vs. 245.24 [218.80, 265.90] pg/mL, Z = -2.464, P = 0.013). BAFF levels in APOs group tended to be higher than that in NAPOs group (416.52 [307.07, 511.12] vs. 259.37 [203.59, 375.81] pg/mL, Z = -2.718, P = 0.006). Compared to HP group, concentrations of IFN-α, interleukin (IL-6) and tumor necrosis factor were higher in patient group (33.37 [18.85, 48.12] vs. 13.10 [6.85, 25.47] pg/mL, Z = -2.023, P = 0.043; 39.16 [4.41, 195.87] vs. 3.37 [2.92, 3.90] pg/mL, Z = -3.650, P < 0.001; 8.23 [2.27, 64.46] vs. 1.53 [1.25, 2.31] pg/mL, Z = -3.604, P < 0.001, respectively). Serum BAFF levels had a positive correlation with the concentrations of both IL-6 and IL-10 (IL-6: r = 0.525, P = 0.002; IL-10: r = 0.438, P = 0.012).
Serum BAFF levels are increased in patients with positive aPLs and previous APOs as compared to healthy pregnant females and tend to be higher in individuals with current APOs. The BAFF levels have a positive correlation with serum IL-6 and IL-10.
B细胞活化因子(BAFF)对B细胞存活至关重要。血栓性抗磷脂综合征患者血清BAFF水平升高,但对于抗磷脂抗体(aPLs)阳性且既往有不良妊娠结局(APO)的患者,其血清BAFF水平情况知之甚少。我们旨在分析这些患者孕早期血清BAFF浓度以及不同的妊娠结局。
选取2018年10月至2019年3月在北京大学第三医院就诊的36例aPLs阳性且既往有APO的孕妇(患者组)、25例健康孕妇(HP组)和35例健康非孕女性(HNP组)纳入本研究。收集HNP组、患者组以及HP组孕早期血清。采用酶联免疫吸附测定试剂盒检测血清BAFF和干扰素-α(IFN-α)浓度。采用细胞因子微球阵列分析检测血清细胞因子浓度。根据妊娠结局,将患者组进一步分为APO组和非APO组(NAPO组)、胎儿丢失组和活产组。采用Mann-Whitney U检验评估组间及组内差异的显著性。采用Spearman等级相关分析评估BAFF与相关细胞因子之间的相关系数。
HP组血清BAFF水平显著低于HNP组(245.24 [218.80, 265.90] 对326.94 [267.31, 414.80] pg/mL,Z = -3.966,P < 0.001)。与HP组相比,患者组BAFF水平明显升高(307.77 [219.86, 415.65] 对245.24 [218.80, 265.90] pg/mL,Z = -2.464,P = 0.013)。APO组BAFF水平高于NAPO组(416.52 [307.07, 511.12] 对259.37 [203.59, 375.81] pg/mL,Z = -2.718,P = 0.006)。与HP组相比,患者组IFN-α、白细胞介素(IL-6)和肿瘤坏死因子浓度更高(33.37 [18.85, 48.12] 对13.10 [6.85, 25.47] pg/mL,Z = -2.023,P = 0.043;39.16 [4.41, 195.87] 对3.37 [2.92, 3.90] pg/mL,Z = -3.650,P < 0.001;8.23 [2.27, 64.46] 对1.53 [1.25, 2.31] pg/mL,Z = -3.604,P < 0.001)。血清BAFF水平与IL-6和IL-10浓度均呈正相关(IL-6:r = 0.525,P = 0.002;IL-10:r = 0.438,P = 0.012)。
与健康孕妇相比,aPLs阳性且既往有APO的患者血清BAFF水平升高,且当前有APO的个体血清BAFF水平往往更高。BAFF水平与血清IL-6和IL-10呈正相关。