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血清 B 细胞激活因子 (BAFF) 作为利妥昔单抗诱导 ANCA 相关性血管炎缓解的生物标志物。

Serum B cell activating factor (BAFF) as a biomarker for induction of remission with rituximab in ANCA-associated vasculitis.

机构信息

Division of Allergology and Rheumatology, Department of Diabetes, Endocrinology and Clinical Immunology, School of Medicine, Hyogo Medical University, Nishinomiya, Japan.

Division of Rheumatology, Department of Internal Medicine, Sumitomo Hospital, Nakanoshima, Japan.

出版信息

Immunol Med. 2022 Dec;45(4):238-243. doi: 10.1080/25785826.2022.2094592. Epub 2022 Jul 8.

DOI:10.1080/25785826.2022.2094592
PMID:35802795
Abstract

We examined whether serum B cell activating factor (BAFF) is useful for predicting the remission of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) following rituximab treatment. We used the Birmingham Vasculitis Activity Score (BVAS) 2008 version 3 for the evaluation of 27 patients with AAV 6 months after rituximab treatment. Those with BVAS = 0 achieved remission, whereas those with BVAS score > 0 did not achieve remission. We considered changes in serum BAFF before rituximab treatment, 1 month after treatment, and 6 months after treatment. In the remission group, the serum BAFF increased consistently. In the non-achieved group, serum BAFF was within the normal range. In addition, there was no statistically significant difference between the two groups in terms of serum BAFF before and 1 month after rituximab treatment. However, the serum BAFF level at 6 months after rituximab treatment was significantly higher in the remission group than in the non-achieved group. If serum BAFF does not increase after 6 months of rituximab in AAV, it may be assumed that there are residual B cells and plasma cells in the tissues. Enhanced treatment targeting B cells, including re-administration of rituximab or the addition of other immunosuppressive drugs, should be considered.

摘要

我们研究了血清 B 细胞激活因子 (BAFF) 是否可用于预测利妥昔单抗治疗后抗中性粒细胞胞质抗体 (ANCA) 相关性血管炎 (AAV) 的缓解情况。我们使用 2008 年 Birmingham Vasculitis Activity Score (BVAS) 版本 3 对 27 例接受利妥昔单抗治疗 6 个月后的 AAV 患者进行评估。BVAS = 0 的患者达到缓解,而 BVAS 评分 > 0 的患者未达到缓解。我们考虑了利妥昔单抗治疗前、治疗后 1 个月和治疗后 6 个月时血清 BAFF 的变化。在缓解组中,血清 BAFF 持续增加。在未达到缓解组中,血清 BAFF 在正常范围内。此外,在利妥昔单抗治疗前和治疗后 1 个月两组之间,血清 BAFF 无统计学差异。然而,在利妥昔单抗治疗后 6 个月时,缓解组的血清 BAFF 水平明显高于未达到缓解组。如果 AAV 在利妥昔单抗治疗 6 个月后血清 BAFF 没有增加,则可以假定组织中仍存在 B 细胞和浆细胞。应考虑增强针对 B 细胞的治疗,包括重新给予利妥昔单抗或添加其他免疫抑制剂。

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Impact of NF-κB and reactive oxygen species on intracellular BAFF/APRIL expression in ANCA-associated vasculitis: focusing on the effect of resveratrol.核因子κB和活性氧对ANCA相关性血管炎细胞内BAFF/APRIL表达的影响:聚焦白藜芦醇的作用
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Two Decades Rituximab Therapy in Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis.
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