# From syndromic clues to diagnosis: understanding CARD11-driven disorders

**Authors:** Elena García-Martínez, María Teresa Schiaffino, Marisa Di Natale, María de las Mercedes Díaz Luna, Daniel Alejandro Viteri Álvarez, María Alejandra Mejía González

PMC · DOI: 10.3389/fimmu.2025.1626065 · 2025-06-23

## TL;DR

This paper reviews disorders caused by CARD11 gene mutations, explaining how they lead to immune system issues and how early diagnosis can improve treatment.

## Contribution

The paper provides a comprehensive overview of CARD11-driven immunodeficiencies and their management, highlighting the need for early diagnosis.

## Key findings

- Gain-of-function CARD11 mutations cause BENTA syndrome with uncontrolled NF-κB activity.
- Loss-of-function variants are linked to Hyper-IgE-like syndromes with immunodeficiency and autoimmunity.
- CARD11-related diseases may be underdiagnosed due to overlap with other immune and hematological disorders.

## Abstract

CARD11 is primarily expressed in hematopoietic tissues and lymphocytes and plays a crucial role in the proper activation of B and T cells in response to antigen recognition. Pathogenic variants in the CARD11 gene result in a broad spectrum of syndromic immunodeficiencies with variable severity and clinical outcomes. Gain-of-function mutations lead to uncontrolled NF-κB activity in lymphocytes and are associated with BENTA syndrome (B-cell Expansion with NF-κB and T-cell Anergy), an autosomal dominant disorder characterized by resistance to conventional therapies used for lymphoproliferative conditions. In contrast, loss-of-function variants are linked to Hyper-IgE-like syndromes, presenting with varying degrees of immunodeficiency—ranging from combined immunodeficiency to specific humoral defects—accompanied by atopic manifestations and autoimmunity. CARD11-associated diseases may be more prevalent than previously recognized due to their clinical overlap with atopic and hematological syndromic disorders. Consequently, a high index of suspicion for these conditions facilitates early diagnosis and enables personalized treatment. In this review, we summarize the broad spectrum of CARD11-related diseases, their underlying pathophysiological mechanisms, multidisciplinary management strategies, and current therapeutic options, along with potential future approaches.

## Linked entities

- **Genes:** CARD11 (caspase recruitment domain family member 11) [NCBI Gene 84433]
- **Proteins:** NFKB1 (nuclear factor kappa B subunit 1)

## Full-text entities

- **Genes:** CARD11 (caspase recruitment domain family member 11) [NCBI Gene 84433] {aka BENTA, BIMP3, CARMA1, IMD11, IMD11A, PPBL}
- **Diseases:** atopic and hematological syndromic disorders (MESH:D006402), lymphoproliferative conditions (MESH:D008232), T-cell Anergy (MESH:D016399), BENTA syndrome (OMIM:616452), autosomal dominant disorder (MESH:D030342), immunodeficiency (MESH:D007153), Hyper-IgE (MESH:D007589)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12229871/full.md

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Source: https://tomesphere.com/paper/PMC12229871