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

2026年6月18日 更新者: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.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

100

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:他の
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的: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).

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
To establish reference values for the nasal and blood type I interferon score in an uninfected adult population aged 18 to 65 years inclusive.
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
To assess the impact of immune parameters on baseline blood and nasal IFN-I scores
時間枠: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
時間枠: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
時間枠: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
時間枠:One day
Establishment of a biobank
One day

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Sophie TROUILLET-ASSANT、Laboratoire Commun de Recherche, Hôpital Lyon Sud, Hospices Civils de Lyon, France

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年8月1日

一次修了 (推定)

2027年8月1日

研究の完了 (推定)

2027年8月1日

試験登録日

最初に提出

2026年6月15日

QC基準を満たした最初の提出物

2026年6月18日

最初の投稿 (実際)

2026年6月24日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月24日

QC基準を満たした最後の更新が送信されました

2026年6月18日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 69HCL26_0579

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米国FDA規制医薬品の研究

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