[Inherited lymphoproliferative disorders]

Rinsho Ketsueki. 2019;60(6):708-715. doi: 10.11406/rinketsu.60.708.
[Article in Japanese]

Abstract

Lymphoproliferative disorders (LPDs) are caused by dysregulated lymphocyte proliferation and include polyclonal benign and monoclonal malignant diseases. LPDs frequently occur in immunocompromized patients, particularly those with primary immunodeficiency disease (PID), a monogenic disease. PID-associated LPD corresponds to inherited LPD. Here, we describe inherited LPD and focus on IKZF1-associated diseases and Epstein-Barr virus-associated LPD, such as ZAP70 deficiency and X-linked lymphoproliferative syndrome type 1 with somatic reversion mosaicism. Disclosing the pathogenesis of inherited LPDs would lead to a broad understanding of LPDs and development of new treatment strategies.

Keywords: IKZF1; Lymphoproliferative disorder; X-linked lymphoproliferative syndrome; ZAP70.

Publication types

  • Review

MeSH terms

  • Epstein-Barr Virus Infections
  • Herpesvirus 4, Human
  • Humans
  • Ikaros Transcription Factor / genetics
  • Immunologic Deficiency Syndromes / complications*
  • Lymphoproliferative Disorders / genetics*

Substances

  • IKZF1 protein, human
  • Ikaros Transcription Factor