5PSQ-175 Cytotoxic T lymphocyte antigen 4 mutations on T reg and abatacept: a paediatric case report

S. Traina, M. Scaldaferri, E. Caiazza, F. Cattel
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Abstract

Background and importance The lymphoproliferative autoimmune syndrome caused by cytotoxic T lymphocyte antigen 4 (CTLA-4) insufficiency is characterised by immune dysregulation, haploinsufficiency and multiorgan disorders. This condition is classified as a rare disease and no drugs are yet registered for treatment. Abatacept, an antirheumatic agent that prevents T lymphocyte activation, was proposed. Aim and objectives To report the clinical record of a 15-year-old female patient with autoimmune disorders. Material and methods In 2015, the patient showed Gilbert pityriasis rosea with significant and diffused lymphoadenopathy, and levothyroxine was prescribed for her hypothyroidism. In July 2018, the patient had chronic urticaria and angio-oedema with a low antihistamine response. In April 2019, she showed persistent fever, asthenia and splenomegaly, associated with multiple lymphoadenopathies, compatible with a lymphoproliferative autoimmune syndrome.1 Functional tests evidenced a significant reduction in CTLA-4 expression on T reg lymphocytes. In November 2019, omalizumab was started instead of levocetirizine with benefit. In February 2020, clinicians from the paediatric infections unit proposed to the internal pharmaceutical committee the use of intravenous abatacept as off-label chronic treatment to manage autoimmune disorders related to CTLA-4 mutations. As the patient was suffering from a rare disease, the pharmacists suggested compassionate use of the drug, as for the DM 07/09/2017, also due to the elevated cost of the therapy chosen. Results The use of abatacept has shown a positive outcome to date (after seven doses), with regression in all lymphoadenopathy sites observed. Moreover, because the patient is successfully responding to intravenous administration in hospital, the ethical committee also approved the switch to the subcutaneous form which can be administered at home. Conclusion and relevance Abatacept use in CTLA-4 mutations on T reg may represent a valid chance of positive disease regression. However, eight months of observation of a single patient is not sufficient and more studies and applications are required. Moreover, a literature research and evaluation led the pharmacist to suggest compassionate use to guarantee the patient’s therapy and to optimise drug governance, not affecting hospital costs. References and/or acknowledgements Schwab, et al. J Allergy Clin Immunol 2018;142:1932–46. Conflict of interest No conflict of interest
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5PSQ-175细胞毒性T淋巴细胞抗原4突变在T reg和abatacept:一个儿科病例报告
背景与重要性细胞毒性T淋巴细胞抗原4 (CTLA-4)功能不全引起的淋巴增生性自身免疫性综合征以免疫失调、单倍体功能不全和多器官功能紊乱为特征。这种情况被归类为罕见病,目前还没有药物注册用于治疗。Abatacept是一种抗风湿剂,可防止T淋巴细胞活化。目的报告1例15岁女性自身免疫性疾病患者的临床记录。材料与方法2015年患者出现玫瑰性吉尔伯特糠疹伴明显弥漫性淋巴腺病变,因甲状腺功能减退给予左旋甲状腺素治疗。2018年7月,患者出现慢性荨麻疹和血管水肿,抗组胺反应低。2019年4月,患者出现持续发热、虚弱、脾肿大,伴有多发性淋巴腺病,与淋巴增生性自身免疫性综合征相符功能测试显示CTLA-4在T淋巴细胞上的表达显著降低。2019年11月,omalizumab开始使用,而不是左西替利嗪。2020年2月,儿科感染科的临床医生向内部药物委员会提议,使用静脉注射阿巴接受作为标签外慢性治疗,以管理与CTLA-4突变相关的自身免疫性疾病。由于患者患有罕见疾病,药剂师建议同情地使用该药物,至于2017年7月9日的DM,也是由于所选择的治疗费用较高。结果:迄今为止,阿巴肽的使用显示出积极的结果(在七次剂量后),在所有淋巴腺病变部位观察到消退。此外,由于患者在医院对静脉给药反应良好,伦理委员会也批准改用可在家给药的皮下给药。结论和相关性阿巴接受在T细胞CTLA-4突变中使用可能代表了阳性疾病消退的有效机会。然而,单个患者8个月的观察是不够的,需要更多的研究和应用。此外,一项文献研究和评估导致药剂师建议同情使用,以保证患者的治疗和优化药物治理,不影响医院的成本。参考文献和/或致谢Schwab等。[J] .中华过敏杂志,2018;42(2):344 - 344。利益冲突无利益冲突
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