Evidence map›Paper›PMID 34373443›Full record

ArticleCell discovery2021

Integrated single-cell analysis revealed immune dynamics during Ad5-nCoV immunization.

Qiqi Cao, Shipo Wu, Chuanle Xiao, Shuzhen Chen, Xiangyang Chi, Xiuliang Cui, Hao Tang, Wenru Su, Yingfeng Zheng, Jiayong Zhong and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 12% of its field
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
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  15. Upregulated CD8Frontiers in immunology · 2023
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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

16 authors at 5 institutions in 2 countries.

Qiqi Cao *International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University / Naval Medical University, Shanghai, China.
Shipo Wu *Beijing Institute of Biotechnology, Beijing, China.
Chuanle Xiao *State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.ORCID http://orcid.org/0000-0002-4680-0682
Shuzhen Chen *International Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University / Naval Medical University, Shanghai, China.
Xiangyang ChiBeijing Institute of Biotechnology, Beijing, China.
Xiuliang CuiInternational Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University / Naval Medical University, Shanghai, China.
Hao TangDepartment of Respiratory and Critical Care Medicine, Changzheng Hospital, Second Military Medical University / Naval Medical University, Shanghai, China.
Wenru SuState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yingfeng ZhengState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
Jiayong ZhongState Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhaomin LiHuaAn McAb Biotech Company, Hangzhou, Zhejiang, China.
Fang LiHuaAn McAb Biotech Company, Hangzhou, Zhejiang, China.
Haijia ChenGuangzhou SALIAI Stemcell Science and Technology Co., Ltd., Guangzhou, Guangdong, China.
Lihua HouBeijing Institute of Biotechnology, Beijing, China. houlihua@sina.com.
Hongyang WangInternational Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University / Naval Medical University, Shanghai, China. hywangk@vip.sina.com.ORCID http://orcid.org/0000-0002-4709-3334
Wen WenInternational Cooperation Laboratory on Signal Transduction, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University / Naval Medical University, Shanghai, China. wenwen_smmu@163.com.
Second Military Medical University · CNSun Yat-sen University · CNHangzhou DAC Biotech (China) · CNCzech Academy of Sciences, Institute of Biotechnology · CZGCI Science & Technology (China) · CN

Funding

Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2018ZX09101002Ministry of Science and Technology of the People's Republic of China (Chinese Ministry of Science and Technology) 2018ZX10732202-002-001National Natural Science Foundation of China (National Science Foundation of China) 81670015National Natural Science Foundation of China (National Science Foundation of China) 81722034National Natural Science Foundation of China (National Science Foundation of China) 81802878National Natural Science Foundation of China (National Science Foundation of China) 81988101
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19), driven by SARS-CoV-2, is a severe infectious disease that has become a global health threat. Vaccines are among the most effective public health tools for combating COVID-19. Immune status is critical for evaluating the safety and response to the vaccine, however, the evolution of the immune response during immunization remains poorly understood. Single-cell RNA sequencing (scRNA-seq) represents a powerful tool for dissecting multicellular behavior and discovering therapeutic antibodies. Herein, by performing scRNA/V(D)J-seq on peripheral blood mononuclear cells from four COVID-19 vaccine trial participants longitudinally during immunization, we revealed enhanced cellular immunity with concerted and cell type-specific IFN responses as well as boosted humoral immunity with SARS-CoV-2-specific antibodies. Based on the CDR3 sequence and germline enrichment, we were able to identify several potential binding antibodies. We synthesized, expressed and tested 21 clones from the identified lineages. Among them, one monoclonal antibody (P3V6-1) exhibited relatively high affinity with the extracellular domain of Spike protein, which might be a promising therapeutic reagent for COVID-19. Overall, our findings provide insights for assessing vaccine through the novel scRNA/V(D)J-seq approach, which might facilitate the development of more potent, durable and safe prophylactic vaccines.

Identifiers

PMID34373443
PMCPMC8352953
OpenAlexW3188290652

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.