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Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19.
Eto, Shohei; Nukui, Yoko; Tsumura, Miyuki; Nakagama, Yu; Kashimada, Kenichi; Mizoguchi, Yoko; Utsumi, Takanori; Taniguchi, Maki; Sakura, Fumiaki; Noma, Kosuke; Yoshida, Yusuke; Ohshimo, Shinichiro; Nagashima, Shintaro; Okamoto, Keisuke; Endo, Akifumi; Imai, Kohsuke; Kanegane, Hirokazu; Ohnishi, Hidenori; Hirata, Shintaro; Sugiyama, Eiji; Shime, Nobuaki; Ito, Masanori; Ohge, Hiroki; Kido, Yasutoshi; Bastard, Paul; Casanova, Jean-Laurent; Ohara, Osamu; Tanaka, Junko; Morio, Tomohiro; Okada, Satoshi.
  • Eto S; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Nukui Y; Department of Infection Control and Prevention, Tokyo Medical and Dental University Hospital, Tokyo, Japan.
  • Tsumura M; Department of Infection Control and Laboratory Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
  • Nakagama Y; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Kashimada K; Department of Parasitology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
  • Mizoguchi Y; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Utsumi T; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Taniguchi M; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Sakura F; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Noma K; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Yoshida Y; Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Science, 1-2-3 Kasumi, Minami-Ku, Hiroshima-Shi, Hiroshima, 734-8551, Japan.
  • Ohshimo S; Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan.
  • Nagashima S; Department of Emergency and Critical Care Medicine, Hiroshima University Graduate School of Biomedical and Health Science, Hiroshima, Japan.
  • Okamoto K; Department of Epidemiology Infectious Disease Control and Prevention, Hiroshima University Graduate School of Biomedical and Health Sciences, Hiroshima, Japan.
  • Endo A; Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Imai K; Clinical Research Center, Tokyo Medical and Dental University Hospital, Tokyo, Japan.
  • Kanegane H; Department of Community Pediatrics, Perinatal and Maternal Medicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.
  • Ohnishi H; Department of Child Health and Development, Tokyo Medical and Dental University, Tokyo, Japan.
  • Hirata S; Department of Pediatrics, Gifu University Graduate School of Medicine, Gifu, Japan.
  • Sugiyama E; Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan.
  • Shime N; Emeritus Professor of Hiroshima University, Hiroshima, Japan.
  • Ito M; Department of Emergency and Critical Care Medicine, Hiroshima University Graduate School of Biomedical and Health Science, Hiroshima, Japan.
  • Ohge H; Department of General Internal Medicine, Hiroshima University Hospital, Hiroshima, Japan.
  • Kido Y; Department of Infectious Diseases, Hiroshima University Hospital, Hiroshima, Japan.
  • Bastard P; Department of Parasitology, Graduate School of Medicine, Osaka City University, Osaka, Japan.
  • Casanova JL; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Ohara O; University of Paris, Imagine Institute, Paris, France.
  • Tanaka J; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
  • Morio T; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Okada S; University of Paris, Imagine Institute, Paris, France.
J Clin Immunol ; 42(7): 1360-1370, 2022 Oct.
Article in English | MEDLINE | ID: covidwho-1906306
ABSTRACT

PURPOSE:

Autoantibodies (aAbs) to type I interferons (IFNs) have been found in less than 1% of individuals under the age of 60 in the general population, with the prevalence increasing among those over 65. Neutralizing autoantibodies (naAbs) to type I IFNs have been found in at least 15% of patients with life-threatening COVID-19 pneumonia in several cohorts of primarily European descent. We aimed to evaluate the prevalence of aAbs and naAbs to IFN-α2 or IFN-ω in Japanese patients who suffered from COVID-19 as well as in the general population.

METHODS:

Patients who suffered from COVID-19 (n = 622, aged 0-104) and an uninfected healthy control population (n = 3,456, aged 20-91) were enrolled in this study. The severities of the COVID-19 patients were as follows critical (n = 170), severe (n = 235), moderate (n = 112), and mild (n = 105). ELISA and ISRE reporter assays were used to detect aAbs and naAbs to IFN-α2 and IFN-ω using E. coli-produced IFNs.

RESULTS:

In an uninfected general Japanese population aged 20-91, aAbs to IFNs were detected in 0.087% of individuals. By contrast, naAbs to type I IFNs (IFN-α2 and/or IFN-ω, 100 pg/mL) were detected in 10.6% of patients with critical infections, 2.6% of patients with severe infections, and 1% of patients with mild infections. The presence of naAbs to IFNs was significantly associated with critical disease (P = 0.0012), age over 50 (P = 0.0002), and male sex (P = 0.137). A significant but not strong correlation between aAbs and naAbs to IFN-α2 existed (r = - 0.307, p value < 0.0001) reinforced the importance of measuring naAbs in COVID-19 patients, including those of Japanese ancestry.

CONCLUSION:

In this study, we revealed that patients with pre-existing naAbs have a much higher risk of life-threatening COVID-19 pneumonia in Japanese population.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interferon Type I / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Humans / Male Country/Region as subject: Asia Language: English Journal: J Clin Immunol Year: 2022 Document Type: Article Affiliation country: S10875-022-01308-3

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Interferon Type I / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Humans / Male Country/Region as subject: Asia Language: English Journal: J Clin Immunol Year: 2022 Document Type: Article Affiliation country: S10875-022-01308-3