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自体造血干细胞移植后,进展性多发性硬化症的生物标志物减少。

Biomarkers of progressive multiple sclerosis decrease following autologous hematopoietic stem cell transplantation.

作者信息

Erngren Ida, Lundblad Katarina, Pavlovic Ivan, Al-Grety Asma, Larsson Anders, Kultima Kim, Burman Joachim

机构信息

Department of Medical Sciences, Clinical Chemistry, Uppsala University, Uppsala, Sweden.

Department of Medical Sciences, Translational Neurology, Uppsala University, Uppsala, Sweden.

出版信息

J Neuroinflammation. 2025 Jul 17;22(1):186. doi: 10.1186/s12974-025-03511-6.

Abstract

BACKGROUND

Autologous hematopoietic stem cell transplantation (AHSCT) has been increasingly used for treatment of relapsing-remitting multiple sclerosis (RRMS). Existing data suggest that AHSCT might alter the natural course of multiple sclerosis (MS) and postpone or even prevent the occurrence of progressive MS. This study aimed to investigate whether three cerebrospinal fluid biomarkers of progressive MS: Galectin-9, GDF-15, and YKL-40, were affected by treatment intervention with AHSCT for RRMS.

METHODS

RRMS patients treated with AHSCT at Uppsala University Hospital between 2011 and 2018 were considered for participation and included if CSF samples from baseline and at least one follow-up were available. CSF from healthy volunteers was included as controls. Galectin-9 and GDF-15 concentrations were determined with ELISA, and YKL-40 with electrochemiluminescence.

RESULTS

The final cohort comprised 45 RRMS patients and 32 controls. At baseline, MS patients had markedly higher CSF concentrations of Galectin-9 and YKL-40 and slightly higher GDF-15 than controls. Following AHSCT, biomarker concentrations decreased from baseline to the 1-year follow-up, with a median (IQR) of 454 (357-553) vs. 408 (328-495) pg/mL (P = 0.0002) for Galectin-9; 49 (38-79) vs. 45 (35 to 75) pg/mL (P = 0.012) for GDF-15, and 100 (54-164) vs. 58 (43-92) ng/mL (P < 0.0001) for YKL-40. Galectin-9 and YKL-40 concentrations decreased further and were even lower at the 2-year follow-up; median (IQR) 408 (328-495) vs. 376 (289-478) pg/mL (P = 0.0009) for Galectin-9; and 62 (37-96) vs. 56 (30-83) ng/mL (P < 0.0001) for YKL-40. Thereafter, the levels of all biomarkers were stable throughout the follow-up.

CONCLUSION

Treatment with AHSCT was associated with sustained reductions in biomarkers linked to progressive MS, indicating its potential not only to achieve lasting remission but also to delay or prevent transition to SPMS. However, additional studies are necessary to confirm these findings and elucidate their long-term clinical significance.

摘要

背景

自体造血干细胞移植(AHSCT)已越来越多地用于治疗复发缓解型多发性硬化症(RRMS)。现有数据表明,AHSCT可能会改变多发性硬化症(MS)的自然病程,并推迟甚至预防进展型MS的发生。本研究旨在调查进展型MS的三种脑脊液生物标志物:半乳糖凝集素-9、生长分化因子-15(GDF-15)和YKL-40,是否会受到AHSCT治疗RRMS的干预影响。

方法

考虑纳入2011年至2018年在乌普萨拉大学医院接受AHSCT治疗的RRMS患者,若有基线和至少一次随访时的脑脊液样本则纳入研究。纳入健康志愿者的脑脊液作为对照。采用酶联免疫吸附测定法(ELISA)测定半乳糖凝集素-9和GDF-15的浓度,采用电化学发光法测定YKL-40的浓度。

结果

最终队列包括45例RRMS患者和32例对照。基线时,MS患者脑脊液中半乳糖凝集素-9和YKL-40的浓度明显高于对照,GDF-15浓度略高于对照。AHSCT后,生物标志物浓度从基线降至1年随访时,半乳糖凝集素-9的中位数(四分位间距)为454(357 - 553)pg/mL 对408(328 - 495)pg/mL(P = 0.0002);GDF-15为(38 - 79)pg/mL对45(35至75)pg/mL(P = 0.012);YKL-40为100(54 - 164)ng/mL对58(43 - 92)ng/mL(P < 0.0001)。半乳糖凝集素-9和YKL-40浓度在2年随访时进一步降低且更低;半乳糖凝集素-9的中位数(四分位间距)为408(328 - 495)pg/mL对376(289 - 478)pg/mL(P = 0.0009);YKL-40为62(37 - 96)ng/mL对56(30 - 83)ng/mL(P < 0.0001)。此后,所有生物标志物的水平在整个随访期间保持稳定。

结论

AHSCT治疗与进展型MS相关生物标志物的持续降低有关,表明其不仅有可能实现持久缓解,还可能延迟或预防向继发进展型MS(SPMS)的转变。然而,需要更多研究来证实这些发现并阐明其长期临床意义。

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