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Beyond the Pandemic Era: Recent Advances and Efficacy of SARS-CoV-2 Vaccines Against Emerging Variants of Concern.

作者信息

Saha Ankita, Ghosh Roy Sounak, Dwivedi Richa, Tripathi Prajna, Kumar Kamal, Nambiar Shashank Manohar, Pathak Rajiv

机构信息

Department of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, NY 10461, USA.

Henry M. Jackson Foundation for the Advancement of Military Medicine, Naval Medical Research Command, Silver Spring, MD 20910, USA.

出版信息

Vaccines (Basel). 2025 Apr 17;13(4):424. doi: 10.3390/vaccines13040424.


DOI:10.3390/vaccines13040424
PMID:40333293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12031379/
Abstract

Vaccination has been instrumental in curbing the transmission of SARS-CoV-2 and mitigating the severity of clinical manifestations associated with COVID-19. Numerous COVID-19 vaccines have been developed to this effect, including BioNTech-Pfizer and Moderna's mRNA vaccines, as well as adenovirus vector-based vaccines such as Oxford-AstraZeneca. However, the emergence of new variants and subvariants of SARS-CoV-2, characterized by enhanced transmissibility and immune evasion, poses significant challenges to the efficacy of current vaccination strategies. In this review, we aim to comprehensively outline the landscape of emerging SARS-CoV-2 variants of concern (VOCs) and sub-lineages that have recently surfaced in the post-pandemic years. We assess the effectiveness of existing vaccines, including their booster doses, against these emerging variants and subvariants, such as BA.2-derived sub-lineages, XBB sub-lineages, and BA.2.86 (Pirola). Furthermore, we discuss the latest advancements in vaccine technology, including multivalent and pan-coronavirus approaches, along with the development of several next-generation coronavirus vaccines, such as exosome-based, virus-like particle (VLP), mucosal, and nanomaterial-based vaccines. Finally, we highlight the key challenges and critical areas for future research to address the evolving threat of SARS-CoV-2 subvariants and to develop strategies for combating the emergence of new viral threats, thereby improving preparedness for future pandemics.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8739/12031379/c5be0098c5a7/vaccines-13-00424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8739/12031379/c5be0098c5a7/vaccines-13-00424-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8739/12031379/c5be0098c5a7/vaccines-13-00424-g001.jpg

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[1]
Beyond the Pandemic Era: Recent Advances and Efficacy of SARS-CoV-2 Vaccines Against Emerging Variants of Concern.

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[2]
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[3]
MVA-based vaccine candidates expressing SARS-CoV-2 prefusion-stabilized spike proteins of the Wuhan, Beta or Omicron BA.1 variants protect transgenic K18-hACE2 mice against Omicron infection and elicit robust and broad specific humoral and cellular immune responses.

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[4]
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[5]
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[6]
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Vaccines (Basel). 2024-1-30

[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
Immune counter-evolution: immortalized B cell clones can undergo ex vivo directed evolution to counteract viral escape.

Front Immunol. 2025-8-18

[2]
COVID-19 Vaccination Still Makes Sense: Insights on Pneumonia Risk and Hospitalization from a Large-Scale Study at an Academic Tertiary Center in Italy.

Microorganisms. 2025-7-25

[3]
Artificial Intelligence-Driven Strategies for Targeted Delivery and Enhanced Stability of RNA-Based Lipid Nanoparticle Cancer Vaccines.

Pharmaceutics. 2025-7-30

[4]
Adaptation of the Vaccine Prophylaxis Strategy to Variants of the SARS-CoV-2 Virus.

Vaccines (Basel). 2025-7-17

本文引用的文献

[1]
Harnessing Epigenetics: Innovative Approaches in Diagnosing and Combating Viral Acute Respiratory Infections.

Pathogens. 2025-2-1

[2]
Adjuvanted subunit intranasal vaccine reduces SARS-CoV-2 onward transmission in hamsters.

Front Immunol. 2025-2-7

[3]
SARS-CoV-2 Variants: Genetic Insights, Epidemiological Tracking, and Implications for Vaccine Strategies.

Int J Mol Sci. 2025-1-31

[4]
Immunogenicity and safety of a live-attenuated SARS-CoV-2 vaccine candidate based on multiple attenuation mechanisms.

Elife. 2025-2-11

[5]
Recombinant XBB.1.5 boosters induce robust neutralization against KP.2- and KP.3-included JN.1 sublineages.

Signal Transduct Target Ther. 2025-1-27

[6]
Novel vaccine strategies to induce respiratory mucosal immunity: advances and implications.

MedComm (2020). 2025-1-16

[7]
Safety and Immunogenicity of SARS-CoV-2 Spike Receptor-Binding Domain and N-Terminal Domain mRNA Vaccine.

J Infect Dis. 2025-4-15

[8]
Trivalent recombinant protein vaccine induces cross-neutralization against XBB lineage and JN.1 subvariants: preclinical and phase 1 clinical trials.

Nat Commun. 2024-12-30

[9]
Effectiveness of the BNT162b2 XBB.1.5-adapted vaccine against COVID-19 hospitalization related to the JN.1 variant in Europe: a test-negative case-control study using the id.DRIVE platform.

EClinicalMedicine. 2024-12-9

[10]
Evaluating the Effectiveness of mRNA-1273.815 Against COVID-19 Hospitalization Among Adults Aged ≥ 18 Years in the United States.

Infect Dis Ther. 2025-1

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