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N/A N=28 Basic Science

The Impact of Age on Adaptive Immunity in Adults Infected With Respiratory Syncytial Virus

RSV Infection

Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcome: Primary: Number of Participants With Challenge-related Adverse Events — 0; 3 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
RSV A Memphis 37 (Biological)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
Imperial College London
Primary completion
May 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Challenge-related Adverse Events
0; 3
SECONDARY
Symptom Severity in RSV Infection
2.21; 0.75
SECONDARY
Nasal Viral Load Measurement in RSV Infection
28.88; 0.00

Summary

This study will for the first time systematically investigate the immune responses in an elderly cohort challenged with a well-defined RSV inoculum. With a global aging population and continuing difficulties in generating vaccines that can reliably induce protective immunity in the elderly, these data will indicate the targets at which development of vaccines against RSV and other infections should be directed.

Eligibility Criteria

Inclusion Criteria

  • Healthy persons aged 60 to 75 years, able to give informed consent
  • Non smokers or ex-smokers with smokers with less than or equal to 5 pack years smoking history.
  • Spirometry within the normal range for age and height (+/- 15%)
  • FEV1/FVC >70% pre-bronchodilator

Exclusion Criteria

  • Chronic respiratory disease (asthma, COPD, rhinitis, sinusitis) in adulthood
  • Inhaled bronchodilator or steroid use within the last 12 months
  • Habitual use of any medication or other product (prescription or over-the-counter) for symptoms of rhinitis or nasal congestion within the last 3 months
  • Acute upper respiratory infection (URI or sinusitis) in the past 6 weeks
  • Subjects with allergic symptoms present at baseline
  • Clinically relevant abnormality on chest X-ray
  • Those in close domestic contact (i.e. sharing a household with, caring for, or daily face to face contact) with children under 3 years, other elderly adults (>65 years), immunosuppressed persons, or those with chronic respiratory disease
  • Subjects with known or suspected immune deficiency
  • Receipt of systemic glucocorticoids (in a dose ≥ 5 mg prednisone daily or equivalent) within one month, or any other cytotoxic or immunosuppressive drug within 6 months prior to challenge
  • Known IgA deficiency, immotile cilia syndrome, or Kartagener's syndrome
  • History of frequent nose bleeds
  • Any significant medical condition or prescribed drug deemed by the study doctor to make the participant unsuitable for the study
  • Women of childbearing potential must have a negative hCG urine pregnancy test *
  • Positive urine drug screen
  • Women of childbearing potential will have a pregnancy test performed prior to virus inoculation to exclude pregnancy and be required to use contraception throughout the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03728413). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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