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宫内暴露于免疫抑制药物导致新生儿严重联合免疫缺陷筛查异常:自然病史和治疗的病例系列。

In-utero exposure to immunosuppressive medications resulting in abnormal newborn screening for severe combined immunodeficiency: a case series on natural history and management.

机构信息

General Academic Pediatrics, McGaw Medical Center Northwestern University / Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.

Pediatric Allergy/Immunology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.

出版信息

Immunol Res. 2022 Oct;70(5):561-565. doi: 10.1007/s12026-022-09297-6. Epub 2022 Jun 3.

Abstract

Exposure to immunosuppressive medication in utero is an important cause of secondary T cell lymphopenia in infancy, which can be detected via T cell receptor excision circle (TREC) quantification on severe combined immunodeficiency (SCID) newborn screening (NBS). At present, there is a paucity of literature surrounding management of these infants. A protocol including recommendations for vaccinations and follow-up is needed to augment care. Patients referred to immunology for abnormal TREC results on NBS were identified as having in utero exposure to immunosuppressive medications and were followed until lymphopenia improved. The natural history of these patients' lymphopenia was used to develop general management guidelines. Four infants with low TRECs secondary to in utero immunosuppressive exposure were evaluated. Medication exposures included azathioprine, infliximab, hydroxychloroquine, and fingolimod. All infants were born full term. TRECs ranged from 101-206 (normal value in IL ≥ 250 at time of testing, B-actin control). T cell lymphopenia (CD3 < 1500) was present in 50% of cases. Undetectably low effector CD4 naïve T cell population was present in 100% of cases. Mitogen proliferation was uniformly normal. Severity of TREC abnormality did not correlate with presence of T cell lymphopenia. Immune abnormalities normalized in 75% patients by age 4 months. All age-appropriate vaccinations, including live vaccines, were administered to all patients by age 4 months. It is critical to assess for in utero immunosuppressive exposure in infants with abnormal TREC results on NBS. In the infants evaluated, secondary T cell lymphopenia associated with maternal immunosuppressive use resolved or significantly improved by age 4 months. Once abnormal TREC count is deemed to be secondary to in utero immunosuppression and there are no other contraindications, infants may safely receive live vaccination, are able to drink breast milk, and do not require prophylactic anti-microbials.

摘要

在子宫内接触免疫抑制药物是婴儿期继发性 T 细胞淋巴细胞减少症的重要原因,可以通过严重联合免疫缺陷 (SCID) 新生儿筛查 (NBS) 中的 T 细胞受体切除环 (TREC) 定量检测到。目前,围绕这些婴儿的管理方法的文献很少。需要制定包括疫苗接种和随访建议的方案来加强护理。在 NBS 中因 TREC 结果异常而转介到免疫学的患者被认为在子宫内接触免疫抑制药物,并在淋巴细胞减少症改善之前进行随访。这些患者淋巴细胞减少症的自然病史被用于制定一般管理指南。评估了 4 例因宫内免疫抑制暴露而导致 TREC 降低的婴儿。药物暴露包括硫唑嘌呤、英夫利昔单抗、羟氯喹和芬戈莫德。所有婴儿均足月出生。TRECs 范围为 101-206(检测时 IL 中正常值≥250,B-肌动蛋白对照)。50%的病例存在 T 细胞淋巴细胞减少症(CD3<1500)。100%的病例存在无法检测到的低效应 CD4 幼稚 T 细胞群。有丝分裂原增殖均正常。TREC 异常的严重程度与 T 细胞淋巴细胞减少症的存在无关。75%的患者在 4 个月大时免疫异常正常化。所有患者在 4 个月大时均接受了所有年龄适宜的疫苗接种,包括活疫苗。评估 NBS 中 TREC 结果异常的婴儿是否存在宫内免疫抑制暴露至关重要。在评估的婴儿中,与母体免疫抑制药物使用相关的继发性 T 细胞淋巴细胞减少症在 4 个月大时得到缓解或显著改善。一旦异常的 TREC 计数被认为是由宫内免疫抑制引起的,并且没有其他禁忌症,婴儿可以安全地接受活疫苗接种,可以饮用母乳,并且不需要预防性使用抗生素。

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