Evidence map›Paper›PMID 42238391›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Analysis Of Salivary Herpesviruses Reveals Associations Between HHV-6 And Long COVID Severity.

Claire S Laxton, Alexandra Tabachnikova, Lily Cooke, Kexin Wang, Simone Blaser, Julio Silva, Jamie Wood, Henna S Nam, Zhenni Lu, Christine Miller and 10 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

20 authors.

Claire S LaxtonDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-0642-2015
Alexandra TabachnikovaDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0000-0003-4695-2480
Lily CookeDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York.ORCID 0009-0003-9529-0249
Kexin WangDepartment of Biostatistics, Yale School of Public Health, New Haven, CT.
Simone BlaserDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0009-0007-2701-9835
Julio SilvaDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0000-0001-8212-7440
Jamie WoodDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York.
Henna S NamDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.
Zhenni LuDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.
Christine MillerDepartment of Pediatrics, Division of Infectious Diseases and Global Health, Yale School of Medicine New Haven, CT.
Gisele RodriguesCenter for Infection and Immunity, Yale School of Medicine, New Haven, CT.
Victoria FisherCenter for Infection and Immunity, Yale School of Medicine, New Haven, CT.
Christian GuirgisDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.
William B HooperCenter for Infection and Immunity, Yale School of Medicine, New Haven, CT.
Alexandra LeeDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.
Mackenzie DoerstlingDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York.
Bornali BhattacharjeeDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-0801-1543
Leying GuanDepartment of Biostatistics, Yale School of Public Health, New Haven, CT.ORCID 0000-0003-0609-1073
David PutrinoDepartment of Rehabilitation and Human Performance, Icahn School of Medicine at Mount Sinai, New York.ORCID 0000-0002-2232-3324
Akiko IwasakiDepartment of Immunobiology, Yale School of Medicine, New Haven, CT.ORCID 0000-0002-7824-9856

Funding

NRSA Training CoreTL1TR001864 · NCATS · YALE UNIVERSITY · PI CANTLEY, LLOYD G, EDELMAN, E. JENNIFER · 2016 to 2025
$9.9M
IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
NCATS NIH HHS TL1 TR001864NHLBI NIH HHS T32 HL007974
6 · The paper itself

Abstract

Background: Reactivation of human herpesviruses (HHVs), particularly EBV, is associated with more severe acute SARS-CoV-2 infections and the development of Long COVID (LC). Observations of higher anti-EBV antibody levels in individuals with LC support the idea that chronic reactivation of HHVs could contribute to LC pathology. HHV shedding in saliva has also been previously associated with saliva hormone levels. This study aims to examine the relationship between salivary shedding of HHV DNA and LC symptoms, as well as cortisol, testosterone, and estradiol levels. Methods: We enrolled 45 participants with LC, and 45 age-sex-matched controls. Surveys and validated health questionnaires were used to collect demographics, medical history, and symptom profiles. Saliva was self-collected at waking, 15, 30, and 45 minutes, and 8 and 16 hours after waking, across two consecutive days. Salivary cortisol, testosterone and estradiol were measured, and extracted nucleic acid was tested for EBV, HSV 1/2, HCMV and HHV-6 A/B using multiplex qPCR, plus SARS-CoV-2 and RNaseP using RT-qPCR. Findings: Detection of salivary EBV and HHV-6 DNA was highest early in the morning. There were no significant differences in salivary cortisol, testosterone, or estradiol, or in EBV or HHV-6 shedding between the LC and control groups. However, salivary HHV-6 DNA levels were positively associated with a greater aggregated LC propensity score, as well as anxiety and depression scores. Interpretation: The observed correlation between salivary HHV-6 shedding and symptom severity suggests HHV-6 may contribute to post-acute disease, though mechanisms remain unclear. While our study did not identify a relationship between salivary EBV shedding and LC, EBV may still play a role at earlier time points in the disease course, or in compartments not sampled here. These findings highlight the potential importance of HHV-6 in LC pathophysiology and underscore the need for longitudinal, multi-compartment studies of herpesvirus reactivation in LC.

Identifiers

PMID42238391
PMCPMC13228757

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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.