We identified germline heterozygous mutations in CTLA4 in members of four families with severe immune dysregulation. Human CTLA4 haploinsufficiency caused dysregulation of FoxP3+ regulatory T (Treg) cells and lymphocytic infiltration of target organs, mimicking Ctla4 homozygous mice. Patients also exhibited a B cell phenotype, with progressive loss of B cells and accumulation of autoreactive CD21lo B cells. This study demonstrates a critical quantitative role for CTLA-4 in human immune homeostasis.

CTLA4 haploinsufficiency and immune dysregulation

Autoimmune enteropathy study with SNP Genotypes (NGS) data on dbGaP (5 participants)

CTLA4 haploinsufficiency and immune dysregulation

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