Rubella Virus-Associated Cutaneous Granulomatous Disease : a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders

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http://hdl.handle.net/10138/299978

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Buchbinder , D , Hauck , F , Albert , M H , Rack , A , Bakhtiar , S , Shcherbina , A , Deripapa , E , Sullivan , K E , Perelygina , L , Eloit , M , Neven , B , Perot , P , Moshous , D , Suarez , F , Bodemer , C , Bonilla , F A , Vaz , L E , Krol , A L , Klein , C , Seppänen , M , Nugent , D J , Singh , J & Ochs , H D 2019 , ' Rubella Virus-Associated Cutaneous Granulomatous Disease : a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders ' , Journal of Clinical Immunology , vol. 39 , no. 1 , pp. 81-89 . https://doi.org/10.1007/s10875-018-0581-0

Julkaisun nimi: Rubella Virus-Associated Cutaneous Granulomatous Disease : a Unique Complication in Immune-Deficient Patients, Not Limited to DNA Repair Disorders
Tekijä: Buchbinder, David; Hauck, Fabian; Albert, Michael H.; Rack, Anita; Bakhtiar, Shahrzad; Shcherbina, Anna; Deripapa, Elena; Sullivan, Kathleen E.; Perelygina, Ludmila; Eloit, Marc; Neven, Benedicte; Perot, Philippe; Moshous, Despina; Suarez, Felipe; Bodemer, Christine; Bonilla, Francisco A.; Vaz, Louise E.; Krol, Alfons L.; Klein, Christoph; Seppänen, Mikko; Nugent, Diane J.; Singh, Jasjit; Ochs, Hans D.
Tekijän organisaatio: Children's Hospital
Clinicum
HUS Children and Adolescents
Päiväys: 2019-01
Kieli: eng
Sivumäärä: 9
Kuuluu julkaisusarjaan: Journal of Clinical Immunology
ISSN: 0271-9142
DOI-tunniste: https://doi.org/10.1007/s10875-018-0581-0
URI: http://hdl.handle.net/10138/299978
Tiivistelmä: The association of immunodeficiency-related vaccine-derived rubella virus (iVDRV) with cutaneous and visceral granulomatous disease has been reported in patients with primary immunodeficiency disorders (PIDs). The majority of these PID patients with rubella-positive granulomas had DNA repair disorders. To support this line of inquiry, we provide additional descriptive data on seven previously reported patients with Nijmegen breakage syndrome (NBS) (n=3) and ataxia telangiectasia (AT) (n=4) as well as eight previously unreported patients with iVDRV-induced cutaneous granulomas and DNA repair disorders including NBS (n=1), AT (n=5), DNA ligase 4 deficiency (n=1), and Artemis deficiency (n=1). We also provide descriptive data on several previously unreported PID patients with iVDRV-induced cutaneous granulomas including cartilage hair hypoplasia (n=1), warts, hypogammaglobulinemia, immunodeficiency, myelokathexis (WHIM) syndrome (n=1), MHC class II deficiency (n=1), Coronin-1A deficiency (n=1), X-linked severe combined immunodeficiency (X-SCID) (n=1), and combined immunodeficiency without a molecular diagnosis (n=1). At the time of this report, the median age of the patients with skin granulomas and DNA repair disorders was 9years (range 3-18). Cutaneous granulomas have been documented in all, while visceral granulomas were observed in six cases (40%). All patients had received rubella virus vaccine. The median duration of time elapsed from vaccination to the development of cutaneous granulomas was 48months (range 2-152). Hematopoietic cell transplantation was reported to result in scarring resolution of cutaneous granulomas in two patients with NBS, one patient with AT, one patient with Artemis deficiency, one patient with DNA Ligase 4 deficiency, one patient with MHC class II deficiency, and one patient with combined immunodeficiency without a known molecular etiology. Of the previously reported and unreported cases, the majority share the diagnosis of a DNA repair disorder. Analysis of additional patients with this complication may clarify determinants of rubella pathogenesis, identify specific immune defects resulting in chronic infection, and may lead to defect-specific therapies.
Avainsanat: DNA ligase 4 deficiency
ataxia telangiectasia
Nijmegen breakage syndrome
Artemis deficiency
combined immunodeficiency
chronic rubella infection resulting in cutaneous granuloma formation
MUTATIONS
3121 General medicine, internal medicine and other clinical medicine
Vertaisarvioitu: Kyllä
Pääsyrajoitteet: openAccess
Rinnakkaistallennettu versio: publishedVersion


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