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Rituximab Administration in Third Trimester of Pregnancy Suppresses Neonatal B-Cell Development

机译:妊娠晚期的利妥昔单抗给药可抑制新生儿B细胞发育

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We describe the effect on the neonate of administration of rituximab to a woman with idiopathic thrombocytopenic purpura (ITP). Rituximab, an anti-CD20 antibody, was given weekly for 4 weeks to a woman with ITP in her third trimester of pregnancy. One month after the last rituximab administration a healthy girl was born. She had normal growth and development during the first six months. At birth, B-lymphocytes were not detectable. Rituximab levels in mother and neonate were 24000 and 6700 ng/mL, respectively. Only 7 cases of rituximab administration during pregnancy were described. No adverse events are described for fetus and neonate. We demonstrate that rituximab passes the placenta and inhibits neonatal B-lymphocyte development. However, after 6 months B-lymphocyte levels normalized and vaccination titres after 10 months were adequate. No infection-related complications occurred. Rituximab administration during pregnancy appears to be safe for the child but further studies are warranted.
机译:我们描述了对特发性血小板减少性紫癜(ITP)的妇女给予利妥昔单抗对新生儿的影响。利妥昔单抗是一种抗CD20抗体,在妊娠中期的三个月中,每周都会向患有ITP的女性提供4周。在最后一次利妥昔单抗给药后一个月,一个健康的女孩出生了。在头六个月中,她的生长和发育正常。出生时无法检测到B淋巴细胞。母亲和新生儿的利妥昔单抗水平分别为24000和6700μng/ mL。仅描述了妊娠期间使用利妥昔单抗的7例病例。没有描述胎儿和新生儿的不良事件。我们证明利妥昔单抗通过胎盘并抑制新生儿B淋巴细胞的发育。但是,在6个月后,B淋巴细胞水平恢复正常,而10个月后的疫苗滴度已经足够。没有发生感染相关的并发症。怀孕期间使用利妥昔单抗对儿童而言似乎是安全的,但有必要进一步研究。

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