Primary immune regulatory disorders for the pediatric hematologist and oncologist: A case-based review

Pediatr Blood Cancer. 2019 May;66(5):e27619. doi: 10.1002/pbc.27619. Epub 2019 Jan 29.

Abstract

An array of monogenic immune defects marked by autoimmunity, lymphoproliferation, and hyperinflammation rather than infections have been described. Primary immune regulatory disorders pose a challenge to pediatric hematologists and oncologists. This paper focuses on primary immune regulatory disorders including autoimmune lymphoproliferative syndrome (ALPS) and ALPS-like syndromes, immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) and IPEX-like disorders, common variable immunodeficiency (CVID), CVID-like, and late-onset combined immunodeficiency (CID) disorders. Hyperinflammatory disorders and those associated with increased susceptibility to lymphoid malignancies are also discussed. Using a case-based approach, a review of clinical pearls germane to the clinical and laboratory evaluation as well as the treatment of these disorders is provided.

Keywords: X-linked; autoimmune lymphoproliferative syndrome; combined immunodeficiency disorders; common variable immunodeficiency; enteropathy; immune dysregulation; polyendocrinopathy; primary immunodeficiency disorder.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Child
  • Child, Preschool
  • Combined Modality Therapy
  • Disease Management
  • Female
  • Hematologic Neoplasms / etiology*
  • Hematologic Neoplasms / pathology
  • Hematologic Neoplasms / therapy*
  • Humans
  • Immunologic Deficiency Syndromes / complications*
  • Infant
  • Male
  • Prognosis