Role of senescent CD4 T cells in breakthrough infection of the new variant strain of SARS-CoV-2 in elderly patients.

Publication date: Jul 03, 2025

In late 2022, Beijing, China saw a large-scale BF. 7 Omicron variant breakthrough infection. However, the impact of COVID-19 vaccines on elderly breakthrough-infected patients’ antibodies and immune cells response was unclear. We recruited 329 inpatients over 65 with BF. 7 breakthrough infections. We analyzed the link between vaccination and survival in 67 sampled patients, investigating changes in antibody levels, cytokine profiles, as well as immune phenotypes. Experiments revealed that while vaccination could raise antibody levels in the elderly, it showed no significant neutralizing activity against the emerging COVID-19 variant XBB. Flow cytometry showed vaccination increased the proportion of CD4 senescent T cells. Moreover, we found that elevated frequencies of CD4 Tsens cells were associated with reduced antigen-specific CD4 T cell activation, diminished IL-2 production, and lower proportions of Tfh cells, which ultimately leading to impaired neutralizing antibody production, particularly against new emerging variants. We found the immunological efficacy of inactivated vaccines in elderly patients is influenced by the proportion of CD4 senescent T cells. Future elderly vaccination strategies need optimization in dose number and timing, and future vaccine design should aim to minimize the generation of CD4 senescent T cells.

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Concepts Keywords
Breakthrough Aged
China Aged, 80 and over
Elderly Antibodies, Neutralizing
Immunological Antibodies, Neutralizing
Antibodies, Viral
Antibodies, Viral
Breakthrough Infections
CD4-Positive T-Lymphocytes
Cellular Senescence
China
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
Male
SARS-CoV-2
Vaccination

Semantics

Type Source Name
disease IDO role
disease MESH breakthrough infection
disease MESH COVID-19
pathway REACTOME Reproduction
drug DRUGBANK Coenzyme M
disease IDO production
pathway REACTOME Immune System
disease MESH infections
disease MESH reinfection
disease IDO blood
disease IDO infection
disease IDO history
disease IDO assay
drug DRUGBANK Flunarizine
drug DRUGBANK Cysteamine
disease IDO protein
drug DRUGBANK Immune Globulin Human
disease IDO reagent
disease IDO process
drug DRUGBANK Water
drug DRUGBANK Hyaluronic acid
drug DRUGBANK Ethanol
drug DRUGBANK Acetylsalicylic acid
disease MESH dyspnea
disease MESH death
drug DRUGBANK Indoleacetic acid
pathway REACTOME Cellular Senescence

Original Article

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