Suppr超能文献

聚乙二醇化腺苷脱氨酶(PEG-ADA)治疗期间,一名罕见的嵌合型腺苷脱氨酶缺乏患者的免疫重建情况。

Immunologic reconstitution during PEG-ADA therapy in an unusual mosaic ADA deficient patient.

作者信息

Liu Ping, Santisteban Ines, Burroughs Lauri M, Ochs Hans D, Torgerson Troy R, Hershfield Michael S, Rawlings David J, Scharenberg Andrew M

机构信息

Department of Pediatrics, University of Washington and Seattle Children's Hospital Research Institute, Seattle, WA, USA.

出版信息

Clin Immunol. 2009 Feb;130(2):162-74. doi: 10.1016/j.clim.2008.08.026. Epub 2008 Oct 25.

Abstract

We report detailed genetic and immunologic studies in a patient diagnosed with adenosine deaminase (ADA) deficiency and combined immune deficiency at age 5 years. At the time of diagnosis, although all other lymphocyte subsets were depleted, circulating CD8(+) T cells with a terminally differentiated phenotype were abundant and expressed normal ADA activity due to a reversion mutation in a CD8(+) T cell or precursor. Over the first 9 months of replacement therapy with PEG-ADA, the patient steadily accumulated mature naïve CD4(+) and CD8(+) T cells, as well as CD4(+)/FOXP3(+) regulatory T cells, consistent with restoration of a functional cellular immune system. While CD19(+) naïve B cells also accumulated in response to PEG-ADA therapy, a high proportion of these B cells exhibited an immature surface marker phenotype even after 9 months, and immunization with neoantigen bacteriophage varphiX174 demonstrated a markedly subnormal humoral immune response. Our observations in this single patient have important implications for gene therapy of human ADA deficiency, as they indicate that ADA expression within even a large circulating lymphocyte population may not be sufficient to support adequate immune reconstitution. They also suggest that an immature surface marker phenotype of the peripheral B cell compartment may be a useful surrogate marker for incomplete humoral immune reconstitution during enzyme replacement, and possibly other forms of hematopoietic cell therapies.

摘要

我们报告了对一名5岁时被诊断为腺苷脱氨酶(ADA)缺乏症和联合免疫缺陷的患者进行的详细基因和免疫学研究。在诊断时,尽管所有其他淋巴细胞亚群均减少,但具有终末分化表型的循环CD8(+) T细胞丰富,并且由于CD8(+) T细胞或前体细胞中的回复突变而表达正常的ADA活性。在接受聚乙二醇化腺苷脱氨酶(PEG-ADA)替代治疗的前9个月中,患者稳步积累了成熟的初始CD4(+)和CD8(+) T细胞,以及CD4(+)/FOXP3(+)调节性T细胞,这与功能性细胞免疫系统的恢复一致。虽然CD19(+)初始B细胞也因PEG-ADA治疗而积累,但即使在9个月后,这些B细胞中仍有很大比例表现出未成熟的表面标志物表型,并且用新抗原噬菌体φX174免疫显示体液免疫反应明显低于正常水平。我们对这名单一患者的观察结果对人类ADA缺乏症的基因治疗具有重要意义,因为它们表明即使在大量循环淋巴细胞群体中ADA表达可能也不足以支持充分的免疫重建。它们还表明外周B细胞区室的未成熟表面标志物表型可能是酶替代治疗期间体液免疫重建不完全的有用替代标志物,并且可能也是其他形式造血细胞治疗的替代标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6a0/2727638/1bc267f6a439/nihms92776f1a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验