Defective B-cell memory in patients with Down syndrome

Ruud H J Verstegen, Gertjan J. Driessen, Sophinus J W Bartol, Carel J M van Noesel, Louis Boon, Mirjam van der Burg, Jacques J M van Dongen, Esther de Vries, Menno C. van Zelm

Research output: Contribution to journalArticleResearchpeer-review

28 Citations (Scopus)

Abstract

Background: Patients with Down syndrome carry immunologic defects, as evidenced by the increased risks for autoimmune diseases, hematologic malignancies, and respiratory tract infections. Moreover, the low numbers of circulating B cells suggest impaired humoral immunity. Objective: We sought to study how immunodeficiency in patients with Down syndrome results from immunologic defects in the B-cell compartment. Methods: We studied blood B-cell subset composition, replication history, somatic hypermutation status, and class-switch recombination in 17 children with Down syndrome. Germinal centers and plasma cells were studied in tonsils from 4 additional children with Down syndrome. Results: Blood transitional B-cell numbers were normal, but naive mature and memory B-cell numbers were reduced despite slightly increased serum B cell-activating factor levels. Germinal centers and plasma cells in tonsils appeared normal, as were serum immunoglobulin levels. CD27+IgD+IgM+ "natural effector" B cells showed reduced proliferation and somatic hypermutation levels, whereas these were normal in CD27+IgD- memory B cells. Furthermore, IgM+ and IgA+, but not IgG+, memory B cells showed impaired molecular signs for antigen selection. The B-cell pattern was highly similar to that of patients with common variable immunodeficiency and a defect in B-cell activation and proliferation. Conclusion: Children with Down syndrome seem capable of normal germinal center and plasma cell formation. Still, blood memory B-cell numbers were reduced and showed impaired molecular maturation of IgA and IgM, which are important for mucosal immunity. The observed molecular defects in circulating IgA and IgM B-cell memory could reflect impaired local responses, which underlie the increased susceptibility to respiratory tract infections of patients with Down syndrome.

Original languageEnglish
Pages (from-to)1346-1353
Number of pages17
JournalJournal of Allergy and Clinical Immunology
Volume134
Issue number6
DOIs
Publication statusPublished - Dec 2014
Externally publishedYes

Keywords

  • antibody
  • B cell
  • common variable immunodeficiency
  • Down syndrome
  • IgA
  • IgM
  • plasma cell
  • selection
  • somatic hypermutation

Cite this