Gut microbial dysbiosis, IgA, and Enterococcus in common variable immunodeficiency with immune dysregulation

Microbiome. 2025 Jan 16;13(1):12. doi: 10.1186/s40168-024-01982-y.

Abstract

Background: Common variable immunodeficiency (CVID) is characterized by hypogammaglobulinemia and recurrent infections. Significant morbidity and mortality are caused by immune dysregulation complications (CVIDid), which affect around one-third of CVID patients and have a poorly understood etiology. Here, we investigate the hypothesis that gut microbial dysbiosis contributes to the inflammation underlying CVIDid.

Results: Bacterial invasion of colonic crypts was observed in CVID (3/15) and X-linked agammaglobulinemia (XLA, 1/3), but not in healthy control (HC, 0/9) biopsies. Fecal gut microbiota was characterized using 16S rRNA-targeted amplicon sequencing. Increased bacterial load, decreased alpha diversity and distinct beta diversity were observed in CVIDid (n = 42) compared to HC (n = 48), and similar results were seen in CVID with IgA deficiency (n = 40) compared to HC. CVIDid and CVID-IgA showed enrichment of the genus Enterococcus, and in vitro studies confirmed the inflammatory potential of Enterococcus gallinarum and Enterococcus hirae in patient monocytes.

Conclusions: This study further supports the hypothesis that a dysregulated gut microbiota, with IgA deficiency as an important driving factor, contributes to systemic inflammation in primary antibody deficiency, and introduces enterococci as potential pathobionts in CVIDid. Video Abstract.

Keywords: Common variable immunodeficiency (CVID); Gut microbiota; Immune dysregulation; Pathobionts.

MeSH terms

  • Adolescent
  • Adult
  • Agammaglobulinemia* / immunology
  • Aged
  • Common Variable Immunodeficiency* / immunology
  • Common Variable Immunodeficiency* / microbiology
  • Dysbiosis* / immunology
  • Dysbiosis* / microbiology
  • Enterococcus* / genetics
  • Enterococcus* / immunology
  • Feces* / microbiology
  • Female
  • Gastrointestinal Microbiome*
  • Genetic Diseases, X-Linked / immunology
  • Genetic Diseases, X-Linked / microbiology
  • Humans
  • IgA Deficiency / immunology
  • IgA Deficiency / microbiology
  • Immunoglobulin A*
  • Inflammation / immunology
  • Inflammation / microbiology
  • Male
  • Middle Aged
  • RNA, Ribosomal, 16S* / genetics
  • Young Adult

Substances

  • Immunoglobulin A
  • RNA, Ribosomal, 16S

Supplementary concepts

  • Bruton type agammaglobulinemia