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Distinct antibody repertoires against endemic human coronaviruses in children and adults.
Khan, Taushif; Rahman, Mahbuba; Ali, Fatima Al; Huang, Susie S Y; Ata, Manar; Zhang, Qian; Bastard, Paul; Liu, Zhiyong; Jouanguy, Emmanuelle; Béziat, Vivien; Cobat, Aurélie; Nasrallah, Gheyath K; Yassine, Hadi M; Smatti, Maria K; Saeed, Amira; Vandernoot, Isabelle; Goffard, Jean-Christophe; Smits, Guillaume; Migeotte, Isabelle; Haerynck, Filomeen; Meyts, Isabelle; Abel, Laurent; Casanova, Jean-Laurent; Hasan, Mohammad R; Marr, Nico.
  • Khan T; Research Branch, Sidra Medicine, Doha, Qatar.
  • Rahman M; Research Branch, Sidra Medicine, Doha, Qatar.
  • Ali FA; Research Branch, Sidra Medicine, Doha, Qatar.
  • Huang SSY; Research Branch, Sidra Medicine, Doha, Qatar.
  • Ata M; Research Branch, Sidra Medicine, Doha, Qatar.
  • Zhang Q; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Bastard P; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Liu Z; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Jouanguy E; University of Paris, Imagine Institute, Paris, France.
  • Béziat V; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Cobat A; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Nasrallah GK; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Yassine HM; University of Paris, Imagine Institute, Paris, France.
  • Smatti MK; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Saeed A; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Vandernoot I; University of Paris, Imagine Institute, Paris, France.
  • Goffard JC; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, Rockefeller University, New York, New York, USA.
  • Smits G; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Hospital for Sick Children, Paris, France.
  • Migeotte I; University of Paris, Imagine Institute, Paris, France.
  • Haerynck F; College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Meyts I; Biomedical Research Center, Qatar University, Doha, Qatar.
  • Abel L; College of Health Sciences, QU Health, Qatar University, Doha, Qatar.
  • Casanova JL; Biomedical Research Center, Qatar University, Doha, Qatar.
  • Hasan MR; Biomedical Research Center, Qatar University, Doha, Qatar.
  • Marr N; Department of Pathology, Sidra Medicine, Doha, Qatar.
JCI Insight ; 6(4)2021 02 22.
Article in English | MEDLINE | ID: covidwho-1047074
ABSTRACT
Four endemic human coronaviruses (HCoVs) are commonly associated with acute respiratory infection in humans. B cell responses to these "common cold" viruses remain incompletely understood. Here we report a comprehensive analysis of CoV-specific antibody repertoires in 231 children and 1168 adults using phage immunoprecipitation sequencing. Seroprevalence of antibodies against endemic HCoVs ranged between approximately 4% and 27% depending on the species and cohort. We identified at least 136 novel linear B cell epitopes. Antibody repertoires against endemic HCoVs were qualitatively different between children and adults in that anti-HCoV IgG specificities more frequently found among children targeted functionally important and structurally conserved regions of the spike, nucleocapsid, and matrix proteins. Moreover, antibody specificities targeting the highly conserved fusion peptide region and S2' cleavage site of the spike protein were broadly cross-reactive with peptides of epidemic human and nonhuman coronaviruses. In contrast, an acidic tandem repeat in the N-terminal region of the Nsp3 subdomain of the HCoV-HKU1 polyprotein was the predominant target of antibody responses in adult donors. Our findings shed light on the dominant species-specific and pan-CoV target sites of human antibody responses to coronavirus infection, thereby providing important insights for the development of prophylactic or therapeutic monoclonal antibodies and vaccine design.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Infections / Coronavirus / Common Cold / Endemic Diseases / Antibodies, Viral Type of study: Cohort study / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Vaccines Limits: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: English Year: 2021 Document Type: Article Affiliation country: Jci.insight.144499

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus Infections / Coronavirus / Common Cold / Endemic Diseases / Antibodies, Viral Type of study: Cohort study / Observational study / Prognostic study / Qualitative research / Randomized controlled trials Topics: Vaccines Limits: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Language: English Year: 2021 Document Type: Article Affiliation country: Jci.insight.144499