Autoantibodies neutralizing type I IFNs in 40% of patients with WNV encephalitis in seven new cohorts
Gervais, A.; Trespidi, F.; Ferrari, A.; Rovida, F.; Marchal, A.; Croce, S.; Cassaniti, I.; Moratti, M.; Uhrlaub, J. L.; Florian, D. M.; Stiasny, K.; Burdino, E.; Angelini, M.; Bizien, L.; Lilleri, D.; Codullo, V.; Freund, T.; Paran, Y.; Gadoth, A.; Biran, R.; Mancon, A.; Lucca, C.; Vogiatzis, S.; Pacenti, M.; Aubart, M.; Zecca, M.; Comoli, P. A.; Avanzini, M.; Fellay, J.; Piralla, A.; Conti, F.; Dolci, A.; Barzon, L.; Ghisetti, V.; Lazzarotto, T.; Cereda, D.; Aiuti, A.; Jouanguy, E.; Bastard, P. R.; MacDonald, M. M.; Rice, C.; Puel, A.; Abel, L.; Rossini, G.; Mileto, D.; Simonin, Y.; Nagy, A.;
10.1101/2025.08.31.25334556 medRxivShow abstract
Mosquito-borne West Nile virus (WNV) infection is a growing global health problem. About 0.5% of infected individuals develop encephalitis. We previously showed that 40% of patients in six cohorts had WNV encephalitis because of circulating auto-antibodies (auto-Abs) neutralizing type I IFNs. In seven new cohorts, we found that the prevalence of auto-Abs was highest (40% [17-44%]) in patients with encephalitis, and very low in a small sample of individuals with asymptomatic or mild infection. In the 13 European, Middle-Eastern and American cohorts available, odds ratios for WNV encephalitis in individuals with these auto-Abs relative to those without them in a large sample of the general population untested for WNV infection range from [~]20 (OR=17.7; 95% CI: 13.8-22.8, p<10-16) for auto-Abs neutralizing only 100 pg/mL IFN-2 and/or IFN-{omega} to >2000 (OR=2218.4; 95% CI: 125.1-39337.7, p<10-16) for auto-Abs neutralizing high concentrations of IFN-2 and high or low concentrations of IFN-{omega}. Pre-existing autoantibodies neutralizing type I IFNs are therefore causal for WNV encephalitis in about 40% of patients. SummaryIn 13 cohorts of individuals with WNV infection, the risk of WNV encephalitis is increased 20 to >2,000 times by circulating auto-Abs neutralizing type I IFNs, depending on the concentration and combination of type I IFNs neutralized and patient age.
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