Evidence map›Paper›PMID 38077368›Full record

ArticleFrontiers in immunology2023

Antibodies to S2 domain of SARS-CoV-2 spike protein in Moderna mRNA vaccinated subjects sustain antibody-dependent NK cell-mediated cell cytotoxicity against Omicron BA.1.

Corey A Balinsky, Le Jiang, Vihasi Jani, Ying Cheng, Zhiwen Zhang, Tatyana Belinskaya, Qi Qiu, Tran Khanh Long, Megan A Schilling, Sarah A Jenkins and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  3. Review
  4. Article
  5. Article
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  9. Review
  10. Antibody-dependent enhancement of coronaviruses.International journal of biological sciences · 2025
    Review
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

15 authors at 4 institutions in 2 countries.

Corey A BalinskyHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Le JiangHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Vihasi JaniHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Ying ChengLeidos, Reston, VA, United States.
Zhiwen ZhangHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Tatyana BelinskayaHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Qi QiuHenry Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD, United States.
Tran Khanh LongVysnova Partners, Inc., Landover, MD, United States.
Megan A SchillingVirology and Emerging Infectious Department, U.S. Naval Medical Research Unit SOUTH, Lima, Peru.
Sarah A JenkinsDiagnostics and Surveillance Department, Naval Medical Research Command, Silver Spring, MD, United States.
Karen S CorsonUS Naval Medical Research Unit-INDO PACIFIC, Singapore, Singapore.
Nicholas J MartinU.S. Naval Medical Research Unit Eurafcent, Sigonella, Italy.
Andrew G LetiziaUS Naval Medical Research Unit-INDO PACIFIC, Singapore, Singapore.
Robert D HontzUS Naval Medical Research Unit-INDO PACIFIC, Singapore, Singapore.
Peifang SunDiagnostics and Surveillance Department, Naval Medical Research Command, Silver Spring, MD, United States.
Henry M. Jackson Foundation · USNaval Medical Research Command · USLeidos (United States) · USNaval Medical Research Unit Six · PE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vaccination with the primary two-dose series of SARS-CoV-2 mRNA protects against infection with the ancestral strain, and limits the presentation of severe disease after re-infection by multiple variants of concern (VOC), including Omicron, despite the lack of a strong neutralizing response to these variants. We compared antibody responses in serum samples collected from mRNA-1273 (Moderna) vaccinated subjects to identify mechanisms of immune escape and cross-protection. Using pseudovirus constructs containing domain-specific amino acid changes representative of Omicron BA.1, combined with domain competition and RBD-antibody depletion, we showed that RBD antibodies were primarily responsible for virus neutralization and variant escape. Antibodies to NTD played a less significant role in antibody neutralization but acted along with RBD to enhance neutralization. S2 of Omicron BA.1 had no impact on neutralization escape, suggesting it is a less critical domain for antibody neutralization; however, it was as capable as S1 at eliciting IgG3 responses and NK-cell mediated, antibody-dependent cell cytotoxicity (ADCC). Antibody neutralization and ADCC activities to RBD, NTD, and S1 were all prone to BA.1 escape. In contrast, ADCC activities to S2 resisted BA.1 escape. In conclusion, S2 antibodies showed potent ADCC function and resisted Omicron BA.1 escape, suggesting that S2 contributes to cross-protection against Omicron BA.1. In line with its conserved nature, S2 may hold promise as a vaccine target against future variants of SARS-CoV-2.

Indexed as

COVID-19Spike Glycoprotein, CoronavirusAntibody-Dependent Cell CytotoxicityHumansImmunoglobulin GKiller Cells, NaturalRNA, MessengerSARS-CoV-2Immunoglobulin GRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2ADCCIgG subclassModerna mRNA vaccineOmicron BA.1S2SARS-CoV-2

Identifiers

PMID38077368
PMCPMC10702584
OpenAlexW4388940970

What OpenQuestion 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 OpenQuestion graph.