Placental and breast milk transfer of belimumab in three patients with systemic lupus erythematosus treated throughout pregnancy.

IF 0.9 Q4 RHEUMATOLOGY
Akitsu Higuchi, Jumpei Saito, Kentaro Fujimori, Takashi Ishikawa, Hiroyo Kawasaki, Eiko Miyagawa, Sawako Abe, Chie Kohno, Chinatsu Takai, Yuka Sano Wada, Toshinao Kawai, Atsuko Murashima, Kayoko Kaneko
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Abstract

The safety of belimumab during pregnancy, particularly in the third trimester, remains unclear. This study aimed to assess the placental and breast milk transfer of belimumab in pregnancies complicated by systemic lupus erythematosus and to evaluate immunological effects and vaccination responses in offspring. We prospectively followed three patients with systemic lupus erythematosus who received belimumab throughout pregnancy. Belimumab concentrations were measured in maternal serum, cord blood, breast milk, and neonatal serum, along with infant development and vaccination histories. Belimumab was continued throughout pregnancy to control refractory thrombocytopenia in two cases and haemolytic anaemia in one case. All patients delivered full-term infants without obstetric complications. Overall, belimumab concentrations in cord blood and neonatal serum were comparable to those in the maternal serum, suggesting transplacental transfer. A decrease in peripheral B and transitional B cells was observed in all neonates at birth, while serum IgG levels and peripheral T cell counts were within normal ranges. Only one infant was diagnosed with a complication (left vesicoureteral reflux). Belimumab concentrations in breast milk were low, and no adverse events occurred in the vaccinated infants. Continuation of belimumab throughout pregnancy may be an option to control refractory disease activity and achieve successful outcomes in pregnancies complicated by systemic lupus erythematosus. However, careful monitoring during pregnancy and postnatal follow-up is essential to ensure safety, given that belimumab can be transferred to the placenta, detected in the neonatal peripheral blood, and affect the neonatal lymphocyte subset counts at birth.

妊娠期治疗的3例系统性红斑狼疮患者的胎盘和母乳移植。
没有宣布。belimumab在妊娠期间,特别是妊娠晚期的安全性尚不清楚。本研究旨在评估贝利姆单抗在妊娠合并系统性红斑狼疮患者的胎盘和母乳转移,并评估其对后代的免疫效应和疫苗接种反应。我们前瞻性地跟踪了三名在怀孕期间接受贝利姆单抗治疗的系统性红斑狼疮患者。在母体血清、脐带血、母乳和新生儿血清以及婴儿发育和疫苗接种史中测量贝利单抗浓度。妊娠期间继续使用贝利单抗治疗,以控制2例难治性血小板减少症和1例溶血性贫血。所有患者均分娩足月婴儿,无产科并发症。总的来说,脐带血和新生儿血清中的贝利单抗浓度与母体血清中的浓度相当,表明贝利单抗转移到胎盘。所有新生儿出生时外周血B细胞和移行性B细胞均减少,血清γ球蛋白和外周血T细胞值在正常范围内。只有一名婴儿被诊断为并发症(左膀胱输尿管反流)。母乳中的贝利单抗浓度很低,接种疫苗的婴儿没有发生不良事件。在整个妊娠期间继续使用贝利单抗可能是控制难治性疾病活动的一种选择,并导致妊娠合并系统性红斑狼疮的成功结局。然而,怀孕期间和产后随访期间的仔细监测对于确保安全性至关重要,因为贝利单抗可以转移到胎盘,在新生儿外周血中检测到,并在出生时影响新生儿淋巴细胞亚群计数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.40
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