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Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines.

Nicholas HernandezGiorgia BucciolLeen MoensJérémie Le PenMohammad ShahrooeiEkaterini Simões GoudourisAfshin ShirkaniMajid Changi-AshtianiHassan Rokni-ZadehEsra Hazar SayarIsmail ReisliAlain Lefevre-UtileDick ZijlmansAndrea JuradoRuben PholienScott B DrutmanSerkan BelkayaAurélie CobatRobbert BoudewijnsDirk JochmansJohan NeytsYoann SeeleuthnerLazaro Lorenzo-DiazChibuzo EnemchukwuIan TietjenHans-Heinrich HoffmannMana MomenilandiLaura PöyhönenMarilda M SiqueiraSheila M Barbosa de LimaDenise C de Souza MatosAkira HommaMaria de Lourdes S MaiaTamiris Azamor da Costa BarrosPatricia Mouta Nunes de OliveiraEmersom Ciclini MesquitaRik GijsbersShen-Ying ZhangStephen J SeligmanLaurent AbelPaul HertzogNico MarrReinaldo de Menezes MartinsIsabelle MeytsQian ZhangMargaret R MacDonaldCharles M RiceJean Laurent CasanovaEmmanuelle JouanguyXavier Bossuyt
Published in: The Journal of experimental medicine (2019)
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 IFNAR2, STAT1, or STAT2). 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 IFNAR1 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 IFNAR1 Autosomal recessive, complete IFNAR1 deficiency can result in life-threatening complications of vaccination with live attenuated measles and YF viruses in previously healthy individuals.
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