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Reduced neutralization against Delta, Gamma, Mu, and Omicron BA.1 variants of SARS-CoV-2 from previous non-Omicron infection.
Pidal, Paola; Fernández, Jorge; Airola, Constanza; Araujo, Miguel; Menjiba, Ana María; Martín, Héctor San; Bruneau, Nicole; Balanda, Monserrat; Elgueta, Coral; Fasce, Rodrigo; Valenzuela, María Teresa; Orellana, Ariel; Ramírez, Eugenio.
  • Pidal P; Microbiología y Control de infecciones asociadas a la atención en Salud, Clínica Indisa, Santiago, Chile.
  • Fernández J; Subdepartment of Molecular Genetics, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Airola C; Epidemiología y Control de infecciones asociadas a la atención en Salud, Clínica Indisa, Santiago, Chile.
  • Araujo M; Unidad de Calidad, Clínica Indisa, Santiago, Chile.
  • Menjiba AM; Unidad de Calidad, Clínica Indisa, Santiago, Chile.
  • Martín HS; Section of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Bruneau N; Section of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Balanda M; Section of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Elgueta C; Section of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Fasce R; Subdepartment of Viral Diseases, Instituto de Salud Pública de Chile, Santiago, Chile.
  • Valenzuela MT; Department of Epidemiology and Public Health, Faculty Medicine, Universidad de los Andes, Santiago, Chile.
  • Orellana A; Facultad de Ciencias de la Vida, Universidad Andrés Bello, Santiago, Chile.
  • Ramírez E; Section of Oncogenic Viruses, Instituto de Salud Pública de Chile, Santiago, Chile. eramirez@ispch.cl.
Med Microbiol Immunol ; 2022 Nov 12.
Article in English | MEDLINE | ID: covidwho-2276465
ABSTRACT
The understanding of the host immune response to SARS-CoV-2 variants of concern is critical for improving diagnostics, therapy development, and vaccines. Here, we analyzed the level of neutralizing antibodies against SARS-CoV-2 D614G, Delta, Gamma, Mu, and Omicron variants in D614G infected healthcare workers during a follow-up up to 6 months after recovery. We followed up 76 patients 60.5% were women and 39.5% men. The 96.1% and 3.9% were symptomatic and asymptomatic, respectively. The most frequent symptoms were headache, myalgia, and cough. The 65.8%, 65.8%, and 92.1% of the infected individuals were positive for neutralizing antibodies against D614G variant at 2, 4, and 6 months of follow-up, respectively. The 26.3%, 48.7% and 65.8% of patients neutralized Delta variant, 19.7%, 32.9% and 52.6% of patients neutralized Gamma, 7.9%, 19.7% and 44.7% of patients neutralized Mu, and 4.0%, 9.2% and 15.8% of patients neutralized Omicron. Low neutralization against Gamma and Mu variants was observed during the follow-up, and very low against the Omicron variant was detected during the same period. The median of neutralizing antibody titers against D614G and Delta variants increased significantly during the follow-up. An association was observed between the levels of neutralizing antibodies against D614G and Delta variants and the severity of the disease. Our results suggest an immune escape from neutralizing antibodies with the Omicron variant because of the many mutations localized in the S protein.
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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Prognostic study Topics: Vaccines / Variants Language: English Year: 2022 Document Type: Article Affiliation country: S00430-022-00753-6

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Prognostic study Topics: Vaccines / Variants Language: English Year: 2022 Document Type: Article Affiliation country: S00430-022-00753-6