Fatal Systemic Granulomatous Disease Associated with Vaccine-Derived Rubella Virus in AIOLOS-Associated Immunodeficiency

We present a case of disseminated granulomatous disease associated with live attenuated vaccine-derived rubella virus (VDRV) in an immunodeficient patient who subsequently developed fatal multi-organ failure, including neurological deficits, with VDRV detected in the cerebrospinal fluid. Posthumous genetic analysis found a heterozygous missense mutation in IKZF3, a gene where haploinsufficiency is linked to immunodeficiency and immune dysregulation. Functional studies demonstrated that this mutation decreases AIOLOS protein stability and half-life, and family members carrying the same mutation exhibited decreased AIOLOS levels. This report underscores the importance of considering persistent rubella virus (RuV) infection in patients with cutaneous granulomatous lesions and highlights the need for comprehensive evaluation to uncover potential underlying immunodeficiencies, which could inform and optimize individualized treatment strategies.

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Publication Details

Journal
Journal of Clinical Immunology
Published
2026-02-26
DOI
https://doi.org/10.1007/s10875-026-01990-7
Citations
1
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
24.43

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Fatal Systemic Granulomatous Disease Associated with Vaccine-Derived Rubella Virus in AIOLOS-Associated Immunodeficiency

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Immunodeficiency and Autoimmune Disorders
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article

Fatal Systemic Granulomatous Disease Associated with Vaccine-Derived Rubella Virus in AIOLOS-Associated Immunodeficiency

Galen Foulke, Karolyn A. Wanat, Linda Zhou, Ludmila Perelygina, Matthew F. Helm, Thomas Leung, M. Rosenbach, Agustin A. Gil Silva, Jennifer Stoddard, Dayna Gager, Kathleen Sullivan, Min-hsin Chen, Hye Sun Kuehn, Julie E. Niemela, LiJuan Hao, Sergio D. Rosenzweig
article en
1 citations

Abstract

We present a case of disseminated granulomatous disease associated with live attenuated vaccine-derived rubella virus (VDRV) in an immunodeficient patient who subsequently developed fatal multi-organ failure, including neurological deficits, with VDRV detected in the cerebrospinal fluid. Posthumous genetic analysis found a heterozygous missense mutation in IKZF3, a gene where haploinsufficiency is linked to immunodeficiency and immune dysregulation. Functional studies demonstrated that this mutation decreases AIOLOS protein stability and half-life, and family members carrying the same mutation exhibited decreased AIOLOS levels. This report underscores the importance of considering persistent rubella virus (RuV) infection in patients with cutaneous granulomatous lesions and highlights the need for comprehensive evaluation to uncover potential underlying immunodeficiencies, which could inform and optimize individualized treatment strategies.

Journal of Clinical ImmunologyVol. 46(1)
Children's Hospital of Philadelphia (US), Medical College of Wisconsin (US), National Institutes of Health Clinical Center (US), University of Pennsylvania (US), Penn State Milton S. Hershey Medical Center (US)
National Institutes of Health, National Institute of Allergy and Infectious Diseases, NIH Clinical Center
Good health and well-being
Openalex Percentile: Top 1%
Immunodeficiency and Autoimmune Disorders
24.43
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