Evidence map›Paper›PMID 38741604›Full record

ArticleResearch (Washington, D.C.)2024

SARS-CoV-2 Omicron Variants Show Attenuated Neurovirulence Compared with the Wild-Type Strain in Elderly Human Brain Spheroids.

Weikang Chen, Xiaobing Jiang, Wei Liang, Haojie Bai, Mingze Xu, Zhe Liu, Lina Yi, Yanming Liu, Yanxia Huang, Yongxin Zhang and 7 more

Abstract read
In one paragraph

Article in Research (Washington, D.C.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Weikang ChenDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Xiaobing JiangDepartment of Neurosurgery/Neuro-Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center (SYSUCC), Guangzhou 510000, China.
Wei LiangInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Haojie BaiInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Mingze XuInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Zhe LiuGuangdong Provincial Institution of Public Health, Guangdong Provincial Center for Disease Control and Prevention, Guangzhou 510000, China.
Lina YiGuangdong Provincial Institution of Public Health, Guangdong Provincial Center for Disease Control and Prevention, Guangzhou 510000, China.
Yanming LiuInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Yanxia HuangDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Yongxin ZhangInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Lixia XuDepartment of Oncology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Baoshu XieDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Nu ZhangDepartment of Neurosurgery, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Jun YuInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Jing LuGuangdong Provincial Institution of Public Health, Guangdong Provincial Center for Disease Control and Prevention, Guangzhou 510000, China.
Haipeng XiaoDepartment of Endocrinology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.
Xiaoxing LiInstitute of Precision Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510000, China.ORCID https://orcid.org/0000-0001-8791-7505

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infection with severe acute respiratory syndrome coronavirus 2 Omicron variants still causes neurological complications in elderly individuals. However, whether and how aging brains are affected by Omicron variants in terms of neuroinvasiveness and neurovirulence are unknown. Here, we utilize resected paracarcinoma brain tissue from elderly individuals to generate primary brain spheroids (BSs) for investigating the replication capability of live wild-type (WT) strain and Omicron (BA.1/BA.2), as well as the mechanisms underlying their neurobiological effects. We find that both WT and Omicron BA.1/BA.2 are able to enter BSs but weakly replicate. There is no difference between Omicron BA.1/BA.2 and WT strains in neurotropism in aging BSs. However, Omicron BA.1/BA.2 exhibits ameliorating neurological damage. Transcriptional profiling indicates that Omicron BA.1/BA.2 induces a lower neuroinflammatory response than WT strain in elderly BSs, suggesting a mechanistic explanation for their attenuated neuropathogenicity. Moreover, we find that both Omicron BA.1/BA.2 and WT strain infections disrupt neural network activity associated with neurodegenerative disorders by causing neuron degeneration and amyloid-β deposition in elderly BSs. These results uncover Omicron-specific mechanisms and cellular immune responses associated with severe acute respiratory syndrome coronavirus 2-induced neurological complications.

Identifiers

PMID38741604
PMCPMC11089278

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.