Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines.
Hernandez N,Bucciol G,Moens L,Le Pen J,Shahrooei M,Goudouris E,Shirkani A,Changi-Ashtiani M,Rokni-Zadeh H,Sayar E,Reisli I,Lefevre-Utile A,Zijlmans D,Jurado A,Pholien R,Drutman S,Belkaya S,Cobat A,Boudewijns R,Jochmans D,Neyts J,Seeleuthner Y,Lorenzo-Diaz L,Enemchukwu C,Tietjen I,Hoffmann H,Momenilandi M,Pöyhönen L,Siqueira M,de Lima S,de Souza Matos D,Homma A,Maia M,da Costa Barros T,de Oliveira P,Mesquita E,Gijsbers R,Zhang S,Seligman S,Abel L,Hertzog P,Marr N,Martins R,Meyts I,Zhang Q,MacDonald M,Rice C,Casanova J,Jouanguy E,Bossuyt X
Source :
J. Exp. Med.
2019 Jul 3
Pmid / DOI:
31270247
Abstract
Vaccination against measles, mumps, and rubella (MMR) and yellow fever (YF) with live attenuated viruses can rarely cause life-threatening disease. Severe illness by MMR vaccines can be caused by inborn errors of type I and/or III interferon (IFN) immunity (mutations in , , or ). Adverse reactions to the YF vaccine have remained unexplained. We report two otherwise healthy patients, a 9-yr-old boy in Iran with severe measles vaccine disease at 1 yr and a 14-yr-old girl in Brazil with viscerotropic disease caused by the YF vaccine at 12 yr. The Iranian patient is homozygous and the Brazilian patient compound heterozygous for loss-of-function variations. Patient-derived fibroblasts are susceptible to viruses, including the YF and measles virus vaccine strains, in the absence or presence of exogenous type I IFN. The patients' fibroblast phenotypes are rescued with WT Autosomal recessive, complete IFNAR1 deficiency can result in life-threatening complications of vaccination with live attenuated measles and YF viruses in previously healthy individuals.© 2019 Hernandez et al.
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