Maternal adalimumab injections produce low levels in breastmilk. Because adalimumab is a large protein molecule, it is likely to be partially destroyed in the infant's gastrointestinal tract and absorption by the infant is probably minimal.[1] Adalimumab was undetectable in the serum of some breastfed infants and adalimumab does not adversely affect the development of breastfed infants or increase the risk of infections. Anti-TNF agents appear to reduce the levels of tumor necrosis factor and IP-10 in the milk of mothers with inflammatory bowel disease in the early postpartum period.[2] Waiting for at least 2 weeks postpartum to resume therapy suspended during pregnancy may minimize transfer to the infant.[3] However, in infants of mothers who received adalimumab during late pregnancy, continued use while breastfeeding does not prolong adalimumab elimination by the infant.[4] Numerous experts and professional guidelines have stated that adalimumab is a low risk to the nursing infant and acceptable to use during breastfeeding.[5-11]
母亲注射阿达木单抗后,母乳中的药物含量较低。由于阿达木单抗是一种大分子蛋白质,它很可能在婴儿胃肠道中被部分破坏,婴儿的吸收量可能极少。[1] 在一些母乳喂养婴儿的血清中未检测到阿达木单抗,且阿达木单抗不会对母乳喂养婴儿的发育产生不利影响,也不会增加感染风险。抗TNF药物似乎会降低产后早期患有炎症性肠病母亲乳汁中肿瘤坏死因子和IP - 10的水平。[2] 等待至少产后2周再恢复孕期暂停的治疗,可能会将药物转移至婴儿的情况降至最低。[3] 然而,对于在妊娠晚期接受阿达木单抗治疗的母亲所生婴儿,母乳喂养期间继续用药并不会延长婴儿体内阿达木单抗的清除时间。[4] 众多专家和专业指南均指出,阿达木单抗对哺乳婴儿的风险较低,母乳喂养期间使用是可接受的。[5 - 11]