Published online August 1, 2005
PEDIATRICS Vol. 116 No. 3 September 2005, pp. e445-e449 (doi:10.1542/peds.2005-0369)
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ELECTRONIC ARTICLE

Novel RAG1 Mutation in a Case of Severe Combined Immunodeficiency

Junyan Zhang, BSc*, Linda Quintal, BSc*, Adelle Atkinson, MD, FRCPC*, Brent Williams, MD{ddagger}, Eyal Grunebaum, MD* and Chaim M. Roifman, MD, FRCPC*

* Divisions of Immunology and Allergy and Program of Infection, Immunity, Injury, and Repair
{ddagger} Hematology and Oncology, Hospital for Sick Children and University of Toronto, Toronto, Canada

Objective. The recombination activating enzymes RAG1 and RAG2 are essential to the process of V(D)J rearrangement in B and T cells and thus to the development of normal immune function. Mutations in RAG1 or RAG2 can lead to a spectrum of disorders, ranging from typical B–T– severe combined immunodeficiency to Omenn's syndrome. We present a unique presentation of RAG1 deficiency.

Patient. We report on a 6-month-old girl who presented with severe respiratory distress, which continued to progress despite antibiotic therapy but seemed to respond to treatment with corticosteroids. The patient exhibited no erythroderma or eosinophilia, and her lymphoid organs were not enlarged.

Results. Investigation of the immune system showed normal numbers of CD3+ T cells, which expressed either CD4 or CD8. Subsequent analysis of the T-cell receptor demonstrated that nearly all CD3+ T cells were clonal; one clone expressed CD4, whereas the other expressed CD8. The extremely restricted T-cell repertoire and the lack of circulating B cells prompted analysis of the RAG1 gene, which revealed a novel homozygous thymine to cytosine substitution at nucleotide position 2686.

Conclusions. This case underscores the importance of more extensive evaluation of the immune system even when widely available, standard, flow cytometric analysis shows normal numbers of T cells that express CD4 or CD8, especially in the absence of circulating B cells.

Key Words: immunodeficiency • gene mutation

Abbreviations: PCR, polymerase chain reaction • SCID, severe combined immunodeficiency • TCR, T-cell receptor

Accepted Mar 3, 2005.


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