• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

慢性特发性血小板减少性紫癜患者体液免疫功能的评估

Evaluation of humoral immune function in patients with chronic idiopathic thrombocytopenic purpura.

作者信息

Rahiminejad Mohammad Saeid, Mirmohammad Sadeghi Mehrdad, Mohammadinejad Payam, Sadeghi Bamdad, Abolhassani Hassan, Dehghani Firoozabadi Mohammad Mehdi, Fathi Seyed Mohammad, Rezvani Hamid, Bahoush Gholamreza, Ehsani Mohammad Ali, Faranoush Mohammad, Mehrvar Azim, Torabi Sagvand Babak, Ghadiani Mojtaba, Rezaei Nima, Aghamohammadi Asghar

机构信息

Research Center for Immunodeficiencies, Children's Medical Center Hospital, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Iran J Allergy Asthma Immunol. 2013 Mar;12(1):50-6.

PMID:23454778
Abstract

Coincidence of autoimmune diseases such as immune thrombocytopenic purpura (ITP) with immunodeficiencies has been reported previously in patients who suffered from primary antibody deficiency (PAD). But there is no original study on immunological profiles of ITP patients to find out their probable immune deficiency. In this case-control study, ITP patients' humoral immunity was investigated for diagnosis of PAD in comparison with normal population. To evaluate the humoral immune system against polysaccharide antigens, patients' serum immunoglobulin levels were measured and a 23-valent pneumococcal capsular polysaccharide vaccine (PPV23) was administrated to evaluate the antibody response to vaccination. In this study, 14 out of 36 patients (39%) were diagnosed with antibody mediated immune deficiency including 2 patients (5.5%) with immunoglobulin class deficiency and 4 (11%) with IgG subclass deficiency. The remaining patients suffered from specific antibody deficiency. The most frequent deficiency in ITP patients was specific antibody deficiency.Therefore, immunological survey on ITP patients may be important especially for those who have undergone splenectomy.

摘要

免疫性血小板减少性紫癜(ITP)等自身免疫性疾病与免疫缺陷的巧合此前已在患有原发性抗体缺陷(PAD)的患者中有所报道。但尚无关于ITP患者免疫特征的原创性研究以查明其可能存在的免疫缺陷。在这项病例对照研究中,与正常人群相比,对ITP患者的体液免疫进行了研究以诊断PAD。为评估针对多糖抗原的体液免疫系统,测量了患者的血清免疫球蛋白水平,并接种了23价肺炎球菌荚膜多糖疫苗(PPV23)以评估对疫苗接种的抗体反应。在本研究中,36例患者中有14例(39%)被诊断为抗体介导的免疫缺陷,其中2例(5.5%)为免疫球蛋白类别缺陷,4例(11%)为IgG亚类缺陷。其余患者患有特异性抗体缺陷。ITP患者中最常见的缺陷是特异性抗体缺陷。因此,对ITP患者进行免疫学检查可能很重要,尤其是对于那些已经接受脾切除术的患者。

相似文献

1
Evaluation of humoral immune function in patients with chronic idiopathic thrombocytopenic purpura.慢性特发性血小板减少性紫癜患者体液免疫功能的评估
Iran J Allergy Asthma Immunol. 2013 Mar;12(1):50-6.
2
A prospective study on antibody response to repeated vaccinations with pneumococcal capsular polysaccharide in splenectomized individuals with special reference to Hodgkin's lymphoma.一项关于脾切除个体(特别提及霍奇金淋巴瘤患者)对肺炎球菌荚膜多糖重复接种疫苗的抗体反应的前瞻性研究。
J Intern Med. 2004 Jun;255(6):664-73. doi: 10.1111/j.1365-2796.2004.01312.x.
3
Anti-beta2-glycoprotein I in childhood immune thrombocytopenic purpura.儿童免疫性血小板减少性紫癜中的抗β2糖蛋白I
Blood Coagul Fibrinolysis. 2008 Jan;19(1):26-31. doi: 10.1097/MBC.0b013e3282eff771.
4
Immunological evaluation of allergic respiratory children with recurrent sinusitis.复发性鼻窦炎变应性呼吸儿童的免疫学评估
Pediatr Allergy Immunol. 2005 Sep;16(6):534-8. doi: 10.1111/j.1399-3038.2005.00303.x.
5
Antigen-specific IgA titres after 23-valent pneumococcal vaccine indicate transient antibody deficiency disease in children.23价肺炎球菌疫苗接种后抗原特异性IgA滴度表明儿童存在短暂性抗体缺乏症。
Vaccine. 2015 Nov 17;33(46):6320-6. doi: 10.1016/j.vaccine.2015.09.041. Epub 2015 Sep 28.
6
Successful use of rituximab in refractory idiopathic thrombocytopenic purpura in a patient with common variable immunodeficiency.利妥昔单抗治疗常见可变免疫缺陷伴难治性特发性血小板减少性紫癜一例
J Investig Allergol Clin Immunol. 2010;20(3):259-62.
7
Validation of current joint American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma and Immunology guidelines for antibody response to the 23-valent pneumococcal vaccine using a population of HIV-infected children.利用一群感染艾滋病毒的儿童对美国过敏、哮喘与免疫学会和美国过敏、哮喘与免疫学院关于23价肺炎球菌疫苗抗体反应的现行联合指南进行验证。
J Allergy Clin Immunol. 2006 Dec;118(6):1336-41. doi: 10.1016/j.jaci.2006.09.036. Epub 2006 Nov 7.
8
B-cell hyperfunction in children with immune thrombocytopenic purpura persists after splenectomy.免疫性血小板减少性紫癜患儿的B细胞功能亢进在脾切除术后持续存在。
Pediatr Res. 2016 Feb;79(2):262-70. doi: 10.1038/pr.2015.211. Epub 2015 Oct 22.
9
Coexistent yellow nail syndrome and selective antibody deficiency.并存的黄甲综合征和选择性抗体缺乏症。
Ann Allergy Asthma Immunol. 2003 Nov;91(5):496-500. doi: 10.1016/S1081-1206(10)61521-9.
10
Antiplatelet antibodies and their correlation with clinical findings in childhood immune thrombocytopenic purpura.抗血小板抗体及其与儿童免疫性血小板减少性紫癜临床发现的相关性。
Acta Haematol. 2005;113(2):109-12. doi: 10.1159/000083448.

引用本文的文献

1
Relationship of primary immune thrombocytopenic purpura and atopia among children: a case control study.儿童原发性免疫性血小板减少性紫癜与特应性的关系:病例对照研究。
Sci Rep. 2020 Jul 16;10(1):11717. doi: 10.1038/s41598-020-68647-2.
2
A mutation in PIK3CD gene causing pediatric systemic lupus erythematosus: A case report.PIK3CD基因的一种突变导致小儿系统性红斑狼疮:病例报告
Medicine (Baltimore). 2019 May;98(18):e15329. doi: 10.1097/MD.0000000000015329.
3
Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.
伊朗的原发性免疫缺陷疾病:国家登记处第三次报告的更新与新见解
J Clin Immunol. 2014 May;34(4):478-90. doi: 10.1007/s10875-014-0001-z.