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高IgM综合征的研究进展 被引量:3

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摘要 高IgM综合征是一种罕见的原发性免疫缺陷病,发病的分子机制涉及到CD40和CD40L。本文拟就高IgM综合征的发病机制及治疗现状进行综述。
出处 《国外医学(输血及血液学分册)》 2004年第3期232-235,共4页 Foreign Medical Sciences(Section of Blood Transfusion and Heanatology)
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同被引文献37

  • 1王玺,陈同辛.高免疫球蛋白M综合征发病机制研究进展[J].国外医学(儿科学分册),2005,32(4):229-231. 被引量:1
  • 2Qamar N, Fuleihan RL. The hyper IgM syndromes [ J ]. Clin Rev Allergy Immunol, 2014, 46(2) : 120 -130.
  • 3A1-Herz W, Bousfdm A, Casanova JL, et al. Primary imnmnodeficieney diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency[ J/OL]. Front Immunol, 2014, 5 : 162.
  • 4Durandy A, Kracker S. Immunoglobulin class-switch recombination deficiencies[J/OL]. Arthritis Res Ther, 2012, 14(4) : 218.
  • 5Peron S, Metin A, Cardes P, et al. Human PMS2 deficiency is associated with impaired immamoglobulin class switch recombination [ J ]. J Exp Med, 2008, 205 ( 11 ) : 2465 - 2472.
  • 6Madkaikar M, Gupta M, Chavan S, et al. X-linked hyper IgM syndrome: clinical, imm~cal and molecular features in patients from India[ J]. Blood Cells Mol Dis, 2014, 53(3) : 99 -104.
  • 7Tsai HY, Yu HH, Chien YH, et al. X-linked hyper-IgM syndrome with CD40LG mutation: two case reports and literature review in Taiwan Residents patients[J]. J Micrebiol Immunol Infect, 2015, 48( 1 ) : 113 -118.
  • 8Lopez-Herrera G, Maravillas-Montero JL, Vargas-Hem,4ndez A, et al. A novel CIMOLG deletion cause the hyper-IgM syndrom with normal CIMOL expression in a 6-month-old child[ J]. Immunol Res, 2015 Mar 10. [Epub ahead of print].
  • 9Cara~o N, CortesAo CS, Reis PH, et al. A novel activation-induced cytidine deaminase (AID) mutation in Brazilian patients with hyper-IgM type 2 syndrom [ J ]. Clin Immunol, 2013, 148 ( 2 ) : 279 - 286.
  • 10Zahn A, Eranki AK, Patenaude AM, et al. Actication induced deaminase C-terminal domain links DNA breaks to end protection and repair during class swtich recombination [ J ]. Proc Nail Acad Sci U S A, 2014, 18(111) : E988 - E997.

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