唐氏综合征患者的免疫特征和感染模式:回顾性回顾

Travis Satnarine , Valishti Pundit , Alana Xavier de Almeida , Matthew Wyke , Gary Kleiner , Melissa Gans
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引用次数: 0

摘要

唐氏综合症(DS)患者已知对感染的易感性增加,但潜在免疫功能障碍的程度仍不清楚。这项回顾性研究评估了退行性椎体滑移患者的免疫异常。电子记录回顾(2010-2023)确定了17例独特患者(平均年龄7.4岁)。复发性感染包括中耳炎(29%)、病毒性uri(24%)和细菌性LRIs(24%),但感染类型通常文献记载较少。实验室异常频繁:15/17(88%)≥1;9/17(53%)患者有绝对淋巴细胞减少症,6/10(60%)患者有T细胞、B细胞和/或nk细胞淋巴减少症。7/14(50%)出现低免疫球蛋白。在初次接种后,9/12(75%)的肺炎球菌滴度无保护作用,只有50%在加强后具有保护作用。干预措施包括额外的肺炎球菌疫苗(8/ 12,67 %)和免疫球蛋白治疗(1/ 17,6 %)。研究结果强调了DS患者免疫异常的高发率,并支持常规免疫评估和量身定制的干预措施。虽然转诊偏倚可能高估了患病率,但结果强调了在这一人群中进行主动免疫监测的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunologic profiles and infection patterns in patients with down syndrome: A retrospective review
Individuals with Down syndrome (DS) are known to have increased susceptibility to infections, yet the extent of underlying immune dysfunction remains under-characterized. This retrospective study evaluates immune abnormalities in individuals with DS referred for immunologic assessment. A review of electronic records (2010–2023) identified 17 unique patients (mean age 7.4 years). Recurrent infections included otitis media (29 %), viral URIs (24 %), and bacterial LRIs (24 %), though infection types were often poorly documented. Lab abnormalities were frequent: 15/17 (88 %) had ≥1; 9/17 (53 %) had absolute lymphopenia, and among those tested, 6/10 (60 %) had T-, B-, and/or NK-cell lymphopenia. Low immunoglobulins were seen in 7/14 (50 %). Pneumococcal titers were non‑protective in 9/12 (75 %) after the primary series, with only 50 % protective post‑booster. Interventions included additional pneumococcal vaccines (8/12, 67 %) and immunoglobulin therapy (1/17, 6 %). Findings underscore the high rate of immune abnormalities in individuals with DS and support routine immunologic evaluation and tailored interventions. Though referral bias may overestimate prevalence, results highlight the need for proactive immune monitoring in this population.
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