Clonal hematopoiesis and acquired thalassemia in common variable immunodeficiency

Mol Med. 1994 Nov;1(1):56-61.

Abstract

Background: Common variable immunodeficiency (CVID) is defined by hypogammaglobulinemia and increased susceptibility to infections. The gene defect responsible for CVID remains unknown.

Methods: During the course of their CVID disease, a female and three male patients developed microcytic anemia. The investigation of this anemia forms the basis for this report.

Results: Reticulocyte globin chain synthesis studies revealed the abnormal alpha/beta ratios that are pathognomonic of thalassemia. Through transcriptional analysis of the glucose-6-phosphate-dehydrogenase (G6PD) locus of the active X-chromosome in blood cells, we determined that the female patient has clonal reticulocytes, platelets, granulocytes, and B and T lymphocytes.

Conclusions: The simultaneous presence of globin synthesis abnormalities and panhypogammaglobulinemia suggests that a common insult at the stem cell level could contribute to the development of CVID and acquired thalassemia.

Publication types

  • Case Reports
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Anemia / complications
  • Anemia / metabolism
  • B-Lymphocytes / pathology
  • Blood Platelets / pathology
  • Child
  • Common Variable Immunodeficiency / complications*
  • Common Variable Immunodeficiency / genetics
  • Common Variable Immunodeficiency / metabolism
  • Female
  • Globins / biosynthesis
  • Glucosephosphate Dehydrogenase / genetics
  • Granulocytes / pathology
  • Haplotypes
  • Hematopoiesis / genetics*
  • Humans
  • Male
  • Polymorphism, Genetic
  • Reticulocytes / pathology
  • T-Lymphocytes / pathology
  • Thalassemia / complications
  • Thalassemia / etiology*
  • Transcription, Genetic
  • X Chromosome

Substances

  • Globins
  • Glucosephosphate Dehydrogenase