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X连锁无丙种球蛋白血症中的自身免疫与炎症

Autoimmunity and inflammation in X-linked agammaglobulinemia.

作者信息

Hernandez-Trujillo Vivian P, Scalchunes Chris, Cunningham-Rundles Charlotte, Ochs Hans D, Bonilla Francisco A, Paris Ken, Yel Leman, Sullivan Kathleen E

机构信息

Division of Allergy and Immunology, Department of Pediatrics, Miami Children's Hospital, 3100 SW 62 Avenue, Miami, FL, 33155, USA,

出版信息

J Clin Immunol. 2014 Aug;34(6):627-32. doi: 10.1007/s10875-014-0056-x. Epub 2014 Jun 10.

Abstract

PURPOSE

In the past, XLA was described as associated with several inflammatory conditions, but with adequate immune globulin treatment, these are presumed to have diminished. The actual prevalence is not known.

METHODS

A web-based patient survey was conducted December 2011- February 2012. Respondents were recruited from the Immune Deficiency Foundation (IDF) patient database, online patient discussion forums and physician recruitment of patients. The questionnaire was developed jointly by IDF and by members of the USIDNET-XLA Disease Specific Working Group. Information regarding inflammatory conditions in patients with XLA was also obtained from the United States Immune Deficiency Network (USIDNET) Registry.

RESULTS

Based on 128 unique patient survey responses, the majority of respondents (69%) reported having at least one inflammatory symptom, with 53% reporting multiple symptoms. However, only 28% had actually been formally diagnosed with an inflammatory condition. Although 20% reported painful joints and 11% reported swelling of the joints, only 7% were given a diagnosis of arthritis. Similarly, 21% reported symptoms of chronic diarrhea and 17% reported abdominal pain, however only 4% had been diagnosed with Crohn's disease. Data from the USIDNET Registry on 149 patients with XLA, revealed that 12% had pain, swelling or arthralgias, while 18% had been diagnosed with arthritis. Similarly, 7% of these patients had abdominal pain and 9% chronic diarrhea.

CONCLUSIONS

Although patients with XLA are generally considered to have a low risk of autoimmune or inflammatory disease compared to other PIDD cohorts, data from this patient survey and a national registry indicate that a significant proportion of patients with XLA have symptoms that are consistent with a diagnosis of arthritis, inflammatory bowel disease or other inflammatory condition. Documented diagnoses of inflammatory diseases were less common but still increased over the general population. Additional data is required to begin implementation of careful monitoring of patients with XLA for these conditions. Early diagnosis and proper treatment may optimize clinical outcomes for these patients.

摘要

目的

过去,X连锁无丙种球蛋白血症(XLA)被描述为与多种炎症性疾病相关,但随着免疫球蛋白治疗的充分应用,这些疾病被认为已经减少。实际患病率尚不清楚。

方法

2011年12月至2012年2月进行了一项基于网络的患者调查。受访者从免疫缺陷基金会(IDF)患者数据库、在线患者讨论论坛以及医生招募的患者中选取。问卷由IDF和美国免疫缺陷网络-XLA疾病特异性工作组的成员共同制定。关于XLA患者炎症性疾病的信息也从美国免疫缺陷网络(USIDNET)登记处获取。

结果

基于128份独特的患者调查回复,大多数受访者(69%)报告至少有一种炎症症状,53%报告有多种症状。然而,只有28%的人实际被正式诊断患有炎症性疾病。虽然20%的人报告有关节疼痛,11%的人报告关节肿胀,但只有7%的人被诊断为关节炎。同样,21%的人报告有慢性腹泻症状,17%的人报告有腹痛,但只有4%的人被诊断为克罗恩病。USIDNET登记处对149例XLA患者的数据显示,12%的人有疼痛、肿胀或关节痛,而18%的人被诊断为关节炎。同样,这些患者中有7%有腹痛,9%有慢性腹泻。

结论

尽管与其他原发性免疫缺陷病(PIDD)队列相比,XLA患者通常被认为自身免疫或炎症性疾病风险较低,但该患者调查和国家登记处的数据表明,相当一部分XLA患者有与关节炎、炎症性肠病或其他炎症性疾病诊断相符的症状。炎症性疾病的确诊病例较少见,但仍高于普通人群。需要更多数据以开始对XLA患者进行这些疾病的仔细监测。早期诊断和适当治疗可能会优化这些患者的临床结局。

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