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Post-vaccination T cell immunity to omicron.
Jacobsen, Henning; Cobos Jiménez, Viviana; Sitaras, Ioannis; Bar-Zeev, Naor; Cicin-Sain, Luka; Higdon, Melissa M; Deloria-Knoll, Maria.
  • Jacobsen H; Department of Viral Immunology, Helmholtz Center for Infection Research, Braunschweig, Germany.
  • Cobos Jiménez V; Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
  • Sitaras I; Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
  • Bar-Zeev N; W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
  • Cicin-Sain L; International Vaccine Access Center, Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, United States.
  • Higdon MM; Department of Viral Immunology, Helmholtz Center for Infection Research, Braunschweig, Germany.
  • Deloria-Knoll M; Centre for Individualised Infection Medicine (CIIM), a joint venture of HZI and MHH, Hannover, Germany.
Front Immunol ; 13: 944713, 2022.
Article in English | MEDLINE | ID: covidwho-2141966
ABSTRACT
In late 2021, the omicron variant of SARS Coronavirus 2 (SARS-CoV-2) emerged and replaced the previously dominant delta strain. Effectiveness of COVID-19 vaccines against omicron has been challenging to estimate in clinical studies or is not available for all vaccines or populations of interest. T cell function can be predictive of vaccine longevity and effectiveness against disease, likely in a more robust way than antibody neutralization. In this mini review, we summarize the evidence on T cell immunity against omicron including effects of boosters, homologous versus heterologous regimens, hybrid immunity, memory responses and vaccine product. Overall, T cell reactivity in post-vaccine specimens is largely preserved against omicron, indicating that vaccines utilizing the parental antigen continue to be protective against disease caused by the omicron variant.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.944713

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Viral Vaccines / COVID-19 Type of study: Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: Front Immunol Year: 2022 Document Type: Article Affiliation country: Fimmu.2022.944713