Tsukuba Research Institute, Sekisui Medical Co. Ltd., Ryugasaki, Japan.
Tsukuba Research Institute, Sekisui Medical Co. Ltd., Ryugasaki, Japan.
Clin Chim Acta. 2014 Mar 20;430:48-54. doi: 10.1016/j.cca.2013.12.039. Epub 2014 Jan 4.
We reported that the soluble LDL receptor relative with 11 ligand-binding repeats (sLR11) is a promising biomarker for follicular lymphoma (FL). In this study, we evaluated the fluctuations in serum sLR11 levels compared with those of serum soluble urokinase-type plasminogen activator receptor (suPAR) and soluble interleukin-2 receptor (sIL-2R) in patients with non-Hodgkin's lymphoma (NHL).
Serum sLR11, suPAR, and sIL-2R levels were measured using ELISA in 175 NHL patients and 57 healthy controls. The levels at diagnosis and at remission were evaluated in 64 paired samples.
Serum sLR11 levels were significantly increased in FL, diffuse large B-cell lymphoma (DLBCL), and peripheral T-cell lymphoma patients compared with healthy controls. Serum sLR11 levels revealed significant positive correlations with serum suPAR and sIL-2R levels. Serum sLR11 levels at remission were decreased compared with those at diagnosis, and the declines at remission expressed a slope of approximately -1 with an intercept near that of controls. The receiver operating characteristic-area under the curve of serum sLR11 concentrations was equivalent to that of serum suPAR and sIL-2R concentrations in an early-stage DLBCL and FL.
sLR11 may be a novel soluble receptor indicative of early-stage NHL, with potential use for evaluating therapeutic efficacy.
我们曾报道,具有 11 个配体结合重复序列的可溶性 LDL 受体相对分子质量(sLR11)是滤泡性淋巴瘤(FL)很有前途的生物标志物。在这项研究中,我们评估了非霍奇金淋巴瘤(NHL)患者血清 sLR11 水平与血清可溶性尿激酶型纤溶酶原激活物受体(suPAR)和可溶性白细胞介素-2 受体(sIL-2R)水平的波动情况。
采用 ELISA 法检测 175 例 NHL 患者和 57 例健康对照者的血清 sLR11、suPAR 和 sIL-2R 水平。在 64 对配对样本中评估了诊断时和缓解时的水平。
与健康对照组相比,FL、弥漫性大 B 细胞淋巴瘤(DLBCL)和外周 T 细胞淋巴瘤患者的血清 sLR11 水平显著升高。血清 sLR11 水平与血清 suPAR 和 sIL-2R 水平呈显著正相关。缓解时的血清 sLR11 水平较诊断时降低,缓解时的下降斜率约为-1,截距接近对照组。在早期 DLBCL 和 FL 中,血清 sLR11 浓度的受试者工作特征曲线下面积与血清 suPAR 和 sIL-2R 浓度相当。
sLR11 可能是一种新型的可溶性受体,提示早期 NHL,具有评估治疗效果的潜力。