Klink D T, van Elburg R M, Schreurs M W J, van Well G T J
Department of Neonatology, VU University Medical Center, De Boelelaan 1117, 1018 HV Amsterdam, The Netherlands.
Clin Dev Immunol. 2008;2008:271363. doi: 10.1155/2008/271363.
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.
我们描述了对一名患有特发性血小板减少性紫癜(ITP)的女性使用利妥昔单抗后对其新生儿的影响。利妥昔单抗是一种抗CD20抗体,在一名处于妊娠晚期的ITP女性患者中每周给药一次,共给药4周。在最后一次利妥昔单抗给药后一个月,一名健康女婴出生。她在头六个月生长发育正常。出生时,未检测到B淋巴细胞。母亲和新生儿体内的利妥昔单抗水平分别为24000 ng/mL和6700 ng/mL。仅描述了7例孕期使用利妥昔单抗的病例。未描述对胎儿和新生儿的不良事件。我们证明利妥昔单抗可通过胎盘并抑制新生儿B淋巴细胞发育。然而,6个月后B淋巴细胞水平恢复正常,10个月后的疫苗接种效价足够。未发生与感染相关的并发症。孕期使用利妥昔单抗对儿童似乎是安全的,但仍需进一步研究。