Evidence map›Paper›PMID 41907060›Full record

ArticleOpen forum infectious diseases2026

Informing the Value of "Boosting" Immunocompetent Adults based on Immune Responses Among US Service Members to SARS-CoV-2 Variants in Late 2024.

Huy C Nguyen, Li Pan, Kerri G Lal, Corey A Balinsky, Jose R Garcia, Dawn L Weir, Irina V Etobayeva, Thomas J McCarthy, Adelbert P Matanza, Lauren Smith and 8 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Huy C NguyenU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.ORCID https://orcid.org/0009-0005-2623-6956
Li PanHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Kerri G LalHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0002-8970-0198
Corey A BalinskyHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Jose R GarciaU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.
Dawn L WeirU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.
Irina V EtobayevaU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.ORCID https://orcid.org/0000-0001-6896-2052
Thomas J McCarthyU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.
Adelbert P MatanzaU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.
Lauren SmithHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.ORCID https://orcid.org/0009-0003-0858-7117
Ying ChengNaval Medical Research Command, Diagnostics and Surveillance Department, Silver Spring, Maryland, USA.
Isabella FoxHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Hao WangHenry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland, USA.
Hayley S FooU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.
Mary Ann SeroteNaval Medical Readiness Training Command Yokosuka, Laboratory Department, Yokosuka, Japan.
Shelly J KrebsWalter Reed Army Institute of Research, US Military HIV Research Program, B Cell Biology, Silver Spring, Maryland, USA.
Peifang SunNaval Medical Research Command, Diagnostics and Surveillance Department, Silver Spring, Maryland, USA.
Andrew G LetiziaU.S. Naval Medical Research Unit INDO PACIFIC, Science Directorate, Singapore, Singapore.ORCID https://orcid.org/0000-0002-7361-5917

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: COVID-19 remains a global biothreat because of new immune-evasive SARS-CoV-2 variants, heterogeneous immunity, and evolving vaccine recommendations. Methods: In this cross-sectional study conducted in September 2024, we evaluated the adaptive immune responses in immunocompetent US active-duty personnel who completed a COVID-19 primary vaccine series but had variable subsequent vaccination and infection histories. We compared responses to 4 circulating variants (JN.1, KP.2, KP.3, LB.1) versus 2 previous dominant vaccine variants (BA.5, XBB.1.5). Analyses were performed based on timing (within or beyond 12 months from enrollment) and type of the most recent exposure, defined as either a COVID-19 vaccination or natural infection. Results: A total of 317 participants were enrolled over 4 weeks in Japan. Significant reduction was observed in receptor binding domain- and spike-specific binding antibodies, neutralization antibodies, antibody-dependent cell cytotoxicity activity, memory B cells, and CD8 Conclusions: Administration of COVID-19 boosters is likely to enhance cross-reactive humoral responses against SARS-CoV-2 circulating variants, potentially facilitating protection from infection and fewer missed work days among military populations. Ongoing surveillance is needed to inform future vaccine composition, timing of administration, and targeted populations to maximize protective benefits.

Indexed as

adaptive immunitySARS-CoV-2US militaryvaccine recommendationsyoung adults

Identifiers

PMID41907060
PMCPMC13023734

What OpenQuestion holds

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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.