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REF-VALUE Study: Establishment of Reference Values for Biomarkers in Healthy Adults (REF-VALUE Stud)

18 juni 2026 uppdaterad av: Hospices Civils de Lyon

Circulating biomarkers play a central role in translational research and precision medicine, particularly for the diagnosis, prognostic, monitoring of inflammatory or infectious diseases and patient stratification. Advances in analytical technologies enable standardised, sensitive and multiplexed assays, but their application remains limited by the lack of reliable reference values derived from well-characterised healthy populations. Indeed, the available data are often heterogeneous and difficult to transfer between platforms.

In this context, the establishment of institutional reference cohorts appears essential for the correct interpretation of immunological parameters-which could be strongly influenced by demographic and clinical factors-and for defining relevant cut-off values when identifying new biomarkers of interest. This issue is particularly critical in the field of viral respiratory infections, where current diagnostic approaches still have several limitations.

Circulating biomarkers play a central role in translational research and precision medicine, particularly for the diagnosis, prognostic, monitoring of inflammatory or infectious diseases and patient stratification. Advances in analytical technologies enable standardised, sensitive and multiplexed assays, but their application remains limited by the lack of reliable reference values derived from well-characterised healthy populations. Indeed, the available data are often heterogeneous and difficult to transfer between platforms.

In this context, the establishment of institutional reference cohorts appears essential for the correct interpretation of immunological parameters-which could be strongly influenced by demographic and clinical factors-and for defining relevant cut-off values when identifying new biomarkers of interest. This issue is particularly critical in the field of viral respiratory infections, where current diagnostic approaches still have several limitations.

Diagnosis is usually based on PCR tests targeting the DNA or RNA of pathogens, requiring a virus-specific test. In practice, only a few viruses (SARS-CoV-2, RSV, influenza) are tested for as a first-line investigation, whilst many other agents may be involved. As a comprehensive approach is difficult to achieve, viral infections often remain under-reported.

Furthermore, the detection of a virus by PCR may indicate either an active infection or residual traces of a past infection. Although viral load can aid interpretation, it does not always allow for a definitive conclusion, making it difficult to distinguish between ongoing viral replication and the persistence of genetic material. It is therefore necessary to have additional markers associated with active infection.

In this context, analysing the host response represents a promising alternative. Viruses induce, in particular, the production of type I interferons (IFN-I), the measurement of which could point the diagnosis towards a viral origin and reflect ongoing infectious activity. However, the interpretation of these biomarkers requires robust reference standards, taking into account their variability across individuals and contexts.

Several studies illustrate the value of such approaches, such as the REFIPA study (NCT07239830), conducted in subjects over 80 years of age, which aims to characterise the immune response, particularly IFN-I, in the context of immunosenescence. This type of study highlights the need for well-phenotyped healthy ? control populations according to age groups and clinical contexts.

Finally, beyond the creation of reference databases, the development of biobanks appears essential. This would enable the establishment of harmonised and directly usable reference values, thereby facilitating translational, basic and pre-clinical research projects, as well as the identification and validation of new biomarkers.

Studieöversikt

Status

Har inte rekryterat ännu

Intervention / Behandling

Studietyp

Interventionell

Inskrivning (Beräknad)

100

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • Participants aged between 18 and 65 years (inclusive)
  • Participants with no known medical conditions
  • Body weight of 50 kg or more

Exclusion Criteria:

  • Participants with symptoms of an active infection (symptom questionnaire or temperature > 37.5°C).

    • Subjects participating in another interventional study with an exclusion period that is still ongoing or that may interfere with this protocol
    • Pregnant women, women in labour or breastfeeding women
    • Individuals deprived of their liberty by a judicial or administrative decision
    • Individuals receiving psychiatric care
    • Individuals admitted to a health or social care facility for purposes other than research
    • Adults subject to legal protection measures (guardianship, curatorship)
    • Individuals not affiliated with a social security scheme or beneficiaries of a similar scheme

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Övrig
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Healthy volunteers
Healthy, uninfected adults aged 18 to 65 inclusive. Participants may be recruited through the press and social media, via the staff mailing list of the Hospices Civils de Lyon, or via posters displayed within the hospital aimed at staff, as well as at patients' carers and any other interested individuals.

The procedures specifically carried out for the study are as follows:

  • 1 nasopharyngeal swab for baseline measurement of the nasal IFN score and to detect the presence of infection
  • Venous blood sample collection:

    • 1 x 2.5 mL PAXgene tube for baseline measurement of the blood IFN score
    • 1 x 4 mL dry tube (serum) to quantify anti-IFN antibody levels
    • 1 x 4 mL heparinized tube to assess non-specific functional immunity.
    • 1 x 2 mL EDTA tube for quantification of circulating leukocyte populations via complete blood count (CBC)
    • 1 x 2 mL EDTA tube for quantification of the main circulating lymphocyte subpopulations via immunophenotyping
    • 2 x 10 mL EDTA tubes and 1 x 4 mL EDTA tube for collection of PBMCs and plasma for biobanking A total of 38.5 mL of venous blood will be collected for the study during a single visit. This volume complies with regulations for subjects weighing at least 50 kg (eligibility criterion).

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
To establish reference values for the nasal and blood type I interferon score in an uninfected adult population aged 18 to 65 years inclusive.
Tidsram: One day
The primary endpoint is the measurement of nasal and blood interferon levels in a population of uninfected adults aged 18 to 65 years inclusive.
One day

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
To assess the impact of immune parameters on baseline blood and nasal IFN-I scores
Tidsram: One day
Correlation between immune parameters assessed by anti-IFN antibody concentration, the abundance of key immune cell subpopulations, lymphocyte function assessed by functional immune testing (such as IGRA), and the baseline blood and nasal interferon score
One day
To assess the impact of demographic and clinical parameters on baseline blood and nasal IFN-I scores
Tidsram: One day
Correlation between demographic (age, sex) and clinical parameters, and the baseline blood and nasal interferon score
One day
Compare baseline IFN-I levels between two subgroups of participants initially considered uninfected: those in whom the PCR test routinely performed on the day of the visit detects no infection, and those in whom this PCR test reveals an asymptomatic infe
Tidsram: One day
Mean (or median) variation in IFN-I between the two groups, with estimation of the effect size (confidence interval) and the level of statistical significance.
One day
Establishment of a biobank
Tidsram: One day
Establishment of a biobank
One day

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Sophie TROUILLET-ASSANT, Laboratoire Commun de Recherche, Hôpital Lyon Sud, Hospices Civils de Lyon, France

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 augusti 2026

Primärt slutförande (Beräknad)

1 augusti 2027

Avslutad studie (Beräknad)

1 augusti 2027

Studieregistreringsdatum

Först inskickad

15 juni 2026

Först inskickad som uppfyllde QC-kriterierna

18 juni 2026

Första postat (Faktisk)

24 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

24 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

18 juni 2026

Senast verifierad

1 juni 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 69HCL26_0579

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