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Infant RSV Immunity Study (IRIS)

11 juin 2026 mis à jour par: Pascal Lavoie, University of British Columbia

Understanding the Impact of Early-life RSV Infections on Infant Immunity and Long-term Health

Respiratory Syncytial Virus (RSV) is a main global cause of respiratory illness and death in infants. Previous infant vaccine trials have failed to demonstrate protection. Moreover, RSV infection during early infancy, particularly in infants younger than 4 months of age, is associated with more severe disease, reduced immune protection, and an increased risk of developing childhood asthma. This study aim to investigate the immunological and long-term health effects of a first exposure to RSV early (<4 months) versus late (>6-9 months) in infancy.

Aperçu de l'étude

Statut

Recrutement

Description détaillée

In British Columbia (Canada), RSV cases rise each year after mid-October, until April, peaking in December. This study compares outcomes between infants born in April to June, who will be naturally exposed to RSV >6-9 months of age versus infants born in September to November, who will be naturally exposed to RSV <4 months of age. Most infants become infected during their first RSV year.

Primary Objectives:

  1. Compare post-season RSV immune responses between the spring cohort of infants born in April to June versus the fall cohort of infants born in September to November.
  2. Compare respiratory outcomes at 3 years of age between the spring cohort of infants born in April to June versus the fall cohort of infants born in September to November.

Secondary Objectives:

  1. Identify immune maturation events linked to stronger post-season RSV antibody responses.
  2. Determine how the gut and upper airway microbiota co-evolve in infants over the first year of life, and how these dynamics shape RSV risk, and are shaped by host-related, and specifically seasonal factors (i.e. Apr-Jun versus Sept-Nov).
  3. Compare immune responses during acute RSV infections between the spring cohort of infants born in April to June versus the fall cohort of infants born in September to November.

Design:

Prospective, observational cohort study of 300 parent-infant pairs born in the spring (April-June) or fall (Sept-Nov), with follow-up at 3 years of age.

Recruitment and Informed Consent Procedure:

Birthing parents planning to give birth at the BC Women's Hospital or live locally in greater Vancouver are identified through the BC Women's Hospital prenatal ultrasound clinic or social media and contacted by the study coordinator in person, by telephone or by text message. Interested participants complete an online eligibility questionnaire and, if eligible, the online consent form. Study advertisements posted in the hospital, local clinics, local community centers and on social media direct interested parents to the study website, online eligibility questionnaire and the study coordinators contact information.

Patients who delivered an infant during the study eligibility period in the Vancouver Coastal Health region are also invited by mail and enrolled prior to the start of the respiratory season for the spring cohort (September/October 2026) or prior to the post-season study visit for the fall cohort (May/June 2027).

Written informed consent is obtained from all participants prior to study procedures. The study has been approved by the University of British Columbia Children's and Women's Research Ethics Board (H25-02623).

Study Procedures:

At enrollment, parents are asked to complete a baseline questionnaire that collects basic pregnancy information (e.g. maternal age, pregnancy conditions, number of babies in pregnancy), intention to receive or receipt of RSV maternal vaccine, household size / number of siblings at home and their ages, smoking, family history of asthma/use of inhalers, use of antibiotics during pregnancy, family history of atopy / asthma, presence of furry pets in the home.

In each post-season questionnaire, parents are also additionally asked about socioeconomic factors, travel, daycare use, child medication use, child hospitalization or medical visit for a respiratory infection and if their child experienced asthma or wheezing symptoms. Study staff review hospital charts at birth and each year after the respiratory season to gather information about RSV-related hospitalizations and RSV testing.

Parents complete a child feeding questionnaire at 3, 6 and 12 months to collect information on infant/child dietary intake including breastfeeding and formula use (start/end dates, duration) and introduction of solid foods.

Biospecimen Collection:

A cord blood sample collected at delivery. If cord blood cannot be collected, a peripheral blood sample is taken at a scheduled study visit within one month after birth, at BC Children's Hospital. If enrolled greater than 1 month after delivery, cord/peripheral blood is not collected. To account for pre-season RSV antibody levels in the analysis, an additional pre-season dried blood spot (DBS) sample are collected in September from the spring cohort babies. We also obtain a residual sample from the Newborn Screening DBS at birth in all infants, for measurements of RSV antibody levels and neutralization titers.

A post-season blood sample is collected from all participants at a scheduled study visit at BC Children's Hospital in May or June following the RSV season.

Serology samples are used to quantify RSV antibodies and neutralization titers, and RSV F-specific antibody-dependent function.

Cord blood and peripheral blood mononuclear cells are stored from the cord and post-natal blood samples, to measure RSV T and B cell responses. A sample is also stored for whole blood RNA-Sequencing studies (PAXgene).

Prenatal and delivery serology samples are obtained from routine samples collected from birthing parents. An additional maternal blood sample is collected at the scheduled post-season study visit in May or June 2027.

RSV Testing and Respiratory Outcome Questionnaires:

Infants are monitored for respiratory outcomes (wheezing episodes) throughout each RSV season (September to March) using parent-completed diaries and parent-collected nasal swab testing when child exhibit pre-defined symptom criteria for infection (e.g. fever, cough, nasal congestion, difficulty breathing).

A subset of infants who test positive for RSV during the acute illness are invited to provide a blood sample about 2 weeks into the acute illness.

Diaries will be used for parents to record each episode of a respiratory infection, the severity and duration of the episode, and to track wheezing days.

Microbiome Studies:

A subset of at least 50 birthing parents in each (Apri-Jun / Sept/Nov) group provide a self-collected vaginal swab within 2 weeks after birth.

Oral swabs are collected from the infants around 2 weeks of age. In addition, stool samples are collected on children at 3, 6, 9 and 12 months of age. For children recruited greater than 1 month after delivery, microbiome samples are not collected.

Main Outcomes:

The study sample size is determined based on the respiratory outcome at 3 years, using the Child Healthy Infant Longitudinal Development study has developed and validated the (CHILDhood Asthma Risk Tool) CHART tool.

The main post-season outcomes are RSV antibody levels and neutralization, with main comparisons between the spring and fall groups/cohorts.

Type d'étude

Observationnel

Inscription (Estimé)

300

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

  • Nom: Pascal Lavoie, MDCM PhD FRCPC
  • Numéro de téléphone: 604-875-2135
  • E-mail: plavoie@bcchr.ca

Sauvegarde des contacts de l'étude

  • Nom: Allison Watts, PhD
  • Numéro de téléphone: 6705 604-875-2000
  • E-mail: awatts@bcchr.ca

Lieux d'étude

    • British Columbia
      • Vancouver, British Columbia, Canada, V6H 3N1
        • Recrutement
        • BC Women's Hospital and Health Centre
        • Contact:
          • Pascal Lavoie, MD PhD
          • Numéro de téléphone: 7318 (604) 875-2000
          • E-mail: plavoie@bcchr.ca
        • Contact:
          • Allison Watts, PhD
          • Numéro de téléphone: 604-875-2135
          • E-mail: awatts@bcchr.ca
        • Chercheur principal:
          • Pascal Lavoie, MD PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

Birthing parents who have a due date or delivery date in April, May or June 2026 (spring group/cohort) or September, October or November 2026 (fall group/cohort) with follow-up of the birthing parent and child during the 2026-2027, 2027-2028 and 2028-2029 RSV seasons. Children will be followed up to 3 years of age. The cohort will consist of 300 birthing parent-child pairs, with 150 in the spring cohort and 150 in the fall cohort. Birthing parents are recruited during antenatal care or shortly after delivery from the ultrasound clinic or delivery wards at BC Women's Hospital, patient lists from local maternity wards within the Vancouver Coastal Health Authority or advertisements at local prenatal care centres (obstetrician, physician and midwife clinics), community centres or on social media.

La description

Inclusion Criteria:

Birthing parent/child pairs with a delivery date in April, May or June or September, October or November who delivered or are planning to deliver at BC Women's Hospital + Health Centre or a nearby, local hospital.

Exclusion Criteria:

Severe pregnancy-related complications or chronic medical conditions in the children making them automatically eligible to receiving RSV immunoprophylaxis in British Columbia (e.g. infants born prematurely < 35 weeks of gestation, or with chronic medical conditions).

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Fall group/cohort
Infants exposed to RSV <4 months of age (born September-November)
Spring group/cohort
Infants exposed to RSV >6-9 months of age (born April-June)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
RSV antibody response
Délai: Post-respiratory season 2027 (May 2027)
i) RSV neutralization titers (expressed as dilution titer to prevent 95% neutralization in vitro; NT95) ii) RSV F-specific antibody-mediated complement activation iii) RSV F-specific antibody-mediated phagocytosis
Post-respiratory season 2027 (May 2027)
Asthma symptoms
Délai: at age 3 years old
Children will be categorized as having low, moderate or high risk of asthma based on asthma-like symptoms defined using the Childhood Asthma Risk Tool (CHART)
at age 3 years old

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Medically attended RSV infections
Délai: At 1 year and 3 years of age
Incidence of RSV and Lower Respiratory Tract Infection hospitalizations and medically attended RSV infections
At 1 year and 3 years of age
Wheezing
Délai: During first RSV season (Sept to April), and each season, up to 3 years of age (for number of wheezing days during season).
Proportion of infants who develop persistent wheezing after their first RSV episode, and the number of wheezing days during season, and after each episode of RSV infection.
During first RSV season (Sept to April), and each season, up to 3 years of age (for number of wheezing days during season).

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Gut and upper airway microbiota
Délai: 0, 3, 6, 9 and 12 months
Characterization of gut and upper airway microbiota, with quantification of within- (α-diversity; Shannon index) and between-sample (β-diversity; Bray-Curtis or UniFrac) diversity.
0, 3, 6, 9 and 12 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

15 janvier 2026

Achèvement primaire (Estimé)

1 juin 2027

Achèvement de l'étude (Estimé)

1 décembre 2029

Dates d'inscription aux études

Première soumission

11 juin 2026

Première soumission répondant aux critères de contrôle qualité

11 juin 2026

Première publication (Réel)

17 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

17 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

11 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • F25-01060

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Description du régime IPD

Pending approval by our local Research Ethics Board.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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