Alessandro Borghesi (@esiborghe) header
Alessandro Borghesi (@esiborghe) profile picture

MD, PhD, Committed to child and neonatal health / human genomics of infectious diseases / windsurfing / caring for the environment

Joined March 2016
Alessandro Borghesi retweeted
Gervais et al. report #autoantibodies neutralizing type I IFNs in three of seven European patients with severe #Usutu virus infection. The patients are males and aged 43–78 years. These autoantibodies are undetectable in the 63 asymptomatic cases tested. hubs.la/Q04D71Tz0
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Alessandro Borghesi retweeted
Autoantibodies neutralizing type I IFNs in 40% of patients with WNV encephalitis in seven new cohorts @jhumimmunity @esiborghe @AurelieCobat @ShenYingZhang1 @casanova_lab @grvsadrian @trespidifra rupress.org/jhi/article/2/3/…
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We also speculate that some patients may initially present with a flu‑like illness (WNVF) and later progress to life‑threatening neuroinvasive disease (WNND) - a two‑step model closely resembling that observed in COVID‑19 pneumonia cell.com/med/fulltext/S2666-…
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Antonio Piralla, Alberto Dolci, Danilo Cereda, Alessandro Aiuti, @JouanguyE, Paul Bastard, and to all the involved Institutions
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Jennifer L. Uhrlaub, Tiziana Lazzarotto, Patrizia Comoli, Marco Zecca, Stefania Croce, Maria Antonietta Avanzini
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In 2022, during an intense WNV summer outbreak, we discovered that a surprisingly high proportion of patients with WNV encephalitis (about half of our initial cohort) carry auto‑Abs neutralizing type I IFNs. Why did we choose to study WNV infection for auto‑Abs to type I IFNs?👇
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...some patients under this definition of WNVF do, at times, die from WNV infection. We concluded that the high proportion of WNVF cases carrying auto‑Abs reflected, at least in some cases, mis‑assignment to the appropriate WNV disease group.
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With time, studies -and colleagues in hospitals and diagnostic centers- began to include in the WNVF “limbo” all patients with clinical signs who for various reasons did not undergo lumbar puncture or imaging to confirm/rule out neurological involvement... acpjournals.org/doi/10.7326/…
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The initial definition of WNVF in the earliest seroepidemiological studies conducted in the USA in the early 2000s referred to individuals tested for WNV serology, self-reporting headache or a transient rise in body temperature in the preceding days thelancet.com/journals/lance…
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Simply because these individuals didn’t have mild disease. 👇
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In the 2023 paper, we observed that about 14% of cases (ranging from 0 in some centers to... 30%!! in others) with mild‑to‑moderate WNVF carried these auto‑Abs. Why did these individuals develop a milder form of the disease, despite the presence of the auto‑Abs? 👇
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When, after the 2023 paper, we studied two new Italian cohorts from the 2023 summer outbreak, we were “happy” to replicate the ~40% auto‑Ab finding. This was already important. But we could not explain yet one finding on mild‑to‑moderate cases with WNV fever (WNVF).
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The 2023 paper was already convincing. Then why replicate and expand it? We could have not, but we did. If you’ve been on top of Everest, don’t you also want to be on top of K2 at some point? Useless to explain that replication and refinement are not optional in Science.
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