A Novel Germline Heterozygous BCL11B Variant Causing Severe Atopic Disease and Immune Dysregulation

B-cell lymphoma/leukemia 11B (BCL11B) is a C2H2 zinc finger transcription factor that is critically important for regulating the development and function of a variety of systems including the central nervous system, the skin, and the immune system. Germline heterozygous variants are associated with...

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Veröffentlicht in:Frontiers in immunology 2021-11, Vol.12, p.788278, Article 788278
Hauptverfasser: Lu, Henry Y., Sertori, Robert, Contreras, Alejandra, Hamer, Mark, Messing, Melina, Del Bel, Kate L., Lopez-Rangel, Elena, Chan, Edmond S., Rehmus, Wingfield, Milner, Joshua D., McNagny, Kelly M., Lehman, Anna, Wiest, David L., Turvey, Stuart E.
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Sprache:eng
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Zusammenfassung:B-cell lymphoma/leukemia 11B (BCL11B) is a C2H2 zinc finger transcription factor that is critically important for regulating the development and function of a variety of systems including the central nervous system, the skin, and the immune system. Germline heterozygous variants are associated with a spectrum of clinical disorders, including severe combined immunodeficiency as well as neurological, craniofacial, and dermal defects. Of these individuals, ~50% present with severe allergic disease. Here, we report the detailed clinical and laboratory workup of one of the most severe BCL11B-dependent atopic cases to date. Leveraging a zebrafish model, we were able to confirm a strong T-cell defect in the patient. Based on these data, we classify germline BCL11B-dependent atopic disease as a novel primary atopic disorder.
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.788278