Skip to content

Cell Mediated Immunity Against RSV and Influenza in a Human Experimental Challenge

Cell Mediated Immunity Against RSV and Influenza in a Human Experimental Challenge

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02755948
Enrollment
75
Registered
2016-04-29
Start date
2012-04-30
Completion date
2020-02-01
Last updated
2024-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Influenza, Human, Respiratory Syncytial Virus Infections

Keywords

Influenza, Respiratory Syncytial Virus Infections, RSV A Memphis 37

Brief summary

Respiratory viruses including influenza and respiratory syncytial virus (RSV) are among the most important causes of severe disease globally, infecting everyone repeatedly throughout life. Understanding of how to prevent infection is incomplete but boosting immunity with vaccines remains the best strategy. T cells have been shown in animals to be essential for clearing respiratory viral infection and are likely to be helpful if stimulated by vaccines. However, where these cells originate from and how they develop in the human lung are still unclear. The investigators will inoculate volunteers with influenza or RSV to examine the relationship between T cells in their blood and lungs and the outcome of infection. By tracking these specialised cells, the investigators aim to develop a better understanding of how they are generated in order to harness them with future vaccines.

Detailed description

Influenza and Respiratory Syncytial Virus (RSV) are the two most common causes of severe viral respiratory tract infection. Seasonal influenza has an overall incidence of 10-20% per annum with frequent complications, and the annual mortality in the USA has been estimated at up to 9.9 deaths per 100,000. According to World Health Organization (WHO) estimates, RSV causes around 64 million infections per annum and 160,000 deaths. It is the leading cause of severe respiratory illness in young children (associated with severe infant wheezing illness) and is also a significant problem in susceptible adults (including the elderly and those with airways disease) in whom RSV is responsible for around 22% of winter respiratory illnesses with a case fatality rate of 2-8%. No vaccines or specific antivirals are available for RSV and those licensed for influenza remain suboptimal. Further understanding of the human immune response to these viruses particularly in the context of the respiratory tract is therefore essential. Experimental human infection studies have the advantage of studying these pathogens in their natural host with the capacity to sample different anatomical sites intensively. Thus the investigators aim to use these models in helping to test vaccines and therapeutics as well as providing critical information on immunity and pathogenesis. The investigators will use previously characterised Good Manufacturing Practices-certified RSV and influenza viruses derived from recent clinical isolates to investigate the response to infection in healthy adult volunteers. Subjects will be recruited via advertisement and screened at Imperial College London. Healthy individuals will be enrolled in the study and undergo baseline investigations including sampling from blood, upper and lower respiratory tract. They will then be inoculated with RSV or influenza by intranasal drops and quarantined for 10 days. During this time, they will have further blood and respiratory sampling. After the 10 day isolation period, they will be discharged and followed up for up to 6 months post-infection. These samples will undergo analysis for antibody, B and T cell responses to correlate with outcome of inoculation, which may include no infection, asymptomatic or symptomatic infection. Thus the investigators will infer the role of immune correlates in protection against infection or symptomatic disease.

Interventions

Good Manufacturing Practices-certified RSV Memphis 37 10(4) PFU in 1 mL 25% sucrose/DMEM delivered by intranasal drops

BIOLOGICALInfluenza A/California/04/2009-likw (H1N1)

Good Manufacturing Practices-certified Influenza A/California/04/09 3.5x10\^6 TCID50 in 1 mL in DPBS delivered by intranasal drops

BIOLOGICALInfluenza A/Belgium/4217/2015 (H3N2)

Good Manufacturing Practices-certified Influenza A/Belgium/4217/2015 (H3N2) 3.5x10\^6 TCID50 in 1 mL in DPBS delivered by intranasal drops

Sponsors

Medical Research Council
CollaboratorOTHER_GOV
Wellcome Trust
CollaboratorOTHER
National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
Imperial College London
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

GMP influenza A/California/04/2009-like (H1N1); influenza A/Belgium/4217/2015 (H3N2); or RSV Memphis 37 virus strains will be used for experimental infection of volunteers.

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

\- Healthy persons aged 18 to 55 years, able to give informed consent

Exclusion criteria

* Chronic respiratory disease (asthma, chronic obstructive pulmonary disease, rhinitis, sinusitis) in adulthood * Inhaled bronchodilator or steroid use within the last 12 months * 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 * Smoking in the past 6 months OR \>5 pack-year lifetime history * Subjects with allergic symptoms present at baseline * Clinically relevant abnormality on chest X-ray * Any ECG abnormality * Those in close domestic contact (i.e. sharing a household with, caring for, or daily face to face contact) with children under 3 years, the elderly (\>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 immunoglobulin A 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 * Pregnant or breastfeeding women * Positive urine drug screen * Detectable baseline haemagglutination inhibition titres against influenza challenge strains * Influenza arm only: history of hypersensitivity to eggs, egg proteins, gentamicin, gelatin or arginine, or with life-threatening reactions to previous influenza vaccinations

Design outcomes

Primary

MeasureTime frameDescription
Total Symptom Score14 daysTotal Symptom Score in infected versus uninfected participants by Jackson's criteria. Eight symptoms were evaluated in the symptom diary: nasal discharge, nasal congestion, sneezing, cough, sore throat, headache, feverishness and fatigue. Subjects were asked to score each symptom 0 (absent), 1 (mild), 2 (moderate), 3 (severe). A clinical cold was defined as 2 out of 3 of: a cumulative 14-day symptom score of ≥14; a subjective feeling of a cold; nasal discharge for ≥3 days. Symptoms were evaluated over a longer period than in Jackson's original description to account for an anticipated slower onset and longer duration of illness with RSV compared with rhinovirus. Maximum cumulative symptom score is therefore 336.

Secondary

MeasureTime frameDescription
Frequency of T Cells in Blood by Flow Cytometry6 monthsPeak Ki-67+ CD38+ CD8+ T cells in the blood by flow cytometry.
Frequency of T Cells in Respiratory Tract by Flow Cytometry6 monthsPeak Ki-67+ CD38+ CD8+ T cells in bronchoalveolar lavage (BAL) by flow cytometry
Viral Load28 daysNasal wash viral load by quantitative polymerase chain reaction (qPCR) (Area under curve)
Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)6 monthsPeak T cells in blood by Enzyme-linked Immunospot (ELISpot). IFNy SFU/million PBMCs (Spot Forming Unit)

Countries

United Kingdom

Participant flow

Participants by arm

ArmCount
RSV A Memphis 37
Participants will be inoculated with RSV Memphis 37 virus. RSV A Memphis 37: Good Manufacturing Practices-certified RSV Memphis 37 10(4) PFU in 1 mL 25% sucrose/DMEM delivered by intranasal drops
41
Influenza A/California/04/2009-like (H1N1)
Participants will be inoculated with Influenza A/California/04/2009-like (H1N1). Influenza A/California/04/2009-likw (H1N1): Good Manufacturing Practices-certified Influenza A/California/04/09 3.5x10\^6 TCID50 in 1 mL in DPBS delivered by intranasal drops
24
Influenza A/Belgium/4217/2015 (H3N2)
Participants will be inoculated with Influenza A/Belgium/4217/2015 (H3N2). Influenza A/Belgium/4217/2015 (H3N2): Good Manufacturing Practices-certified Influenza A/Belgium/4217/2015 (H3N2) 3.5x10\^6 TCID50 in 1 mL in DPBS delivered by intranasal drops
10
Total75

Baseline characteristics

CharacteristicRSV A Memphis 37Influenza A/California/04/2009-like (H1N1)Influenza A/Belgium/4217/2015 (H3N2)Total
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
41 Participants24 Participants10 Participants75 Participants
Age, Continuous26.2 years45.3 years37.2 years33.8 years
Race/Ethnicity, Customized
All other ethnic groups
0 Participants2 Participants0 Participants2 Participants
Race/Ethnicity, Customized
Asian or Asian British (Indian)
0 Participants2 Participants0 Participants2 Participants
Race/Ethnicity, Customized
Asian or Asian British (other)
0 Participants0 Participants1 Participants1 Participants
Race/Ethnicity, Customized
Asian or Asian British (Pakistan)
0 Participants0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Black or Black British (African)
0 Participants3 Participants0 Participants3 Participants
Race/Ethnicity, Customized
Black or Black British (Caribbean)
0 Participants1 Participants0 Participants1 Participants
Race/Ethnicity, Customized
Mixed (White & Caribbean)
0 Participants1 Participants0 Participants1 Participants
Race/Ethnicity, Customized
Mixed White (White & Asian)
0 Participants1 Participants0 Participants1 Participants
Race/Ethnicity, Customized
Unknown
41 Participants0 Participants0 Participants41 Participants
Race/Ethnicity, Customized
White British
0 Participants11 Participants8 Participants19 Participants
Race/Ethnicity, Customized
White Irish
0 Participants1 Participants0 Participants1 Participants
Race/Ethnicity, Customized
White (other)
0 Participants2 Participants1 Participants3 Participants
Region of Enrollment
United Kingdom
41 participants24 participants10 participants75 participants
Sex: Female, Male
Female
12 Participants6 Participants5 Participants23 Participants
Sex: Female, Male
Male
29 Participants18 Participants5 Participants52 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 410 / 240 / 10
other
Total, other adverse events
0 / 410 / 240 / 10
serious
Total, serious adverse events
0 / 410 / 240 / 10

Outcome results

Primary

Total Symptom Score

Total Symptom Score in infected versus uninfected participants by Jackson's criteria. Eight symptoms were evaluated in the symptom diary: nasal discharge, nasal congestion, sneezing, cough, sore throat, headache, feverishness and fatigue. Subjects were asked to score each symptom 0 (absent), 1 (mild), 2 (moderate), 3 (severe). A clinical cold was defined as 2 out of 3 of: a cumulative 14-day symptom score of ≥14; a subjective feeling of a cold; nasal discharge for ≥3 days. Symptoms were evaluated over a longer period than in Jackson's original description to account for an anticipated slower onset and longer duration of illness with RSV compared with rhinovirus. Maximum cumulative symptom score is therefore 336.

Time frame: 14 days

Population: Total number of participants challenged with the specified challenge virus. For the H1N1 arm, only 22 out of 24 participants were analysed because one participant lost their symptom diary and another was excluded from analysis as they had RSV co-infection

ArmMeasureGroupValue (MEDIAN)
RSV A Memphis 37Total Symptom ScoreInfected29.25 score on a scale
RSV A Memphis 37Total Symptom ScoreUninfected13.00 score on a scale
Influenza A/California/04/2009-like (H1N1)Total Symptom ScoreUninfected0 score on a scale
Influenza A/California/04/2009-like (H1N1)Total Symptom ScoreInfected17.50 score on a scale
Influenza A/Belgium/4217/2015 (H3N2)Total Symptom ScoreInfected11.00 score on a scale
Influenza A/Belgium/4217/2015 (H3N2)Total Symptom ScoreUninfected1 score on a scale
Secondary

Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)

Peak T cells in blood by Enzyme-linked Immunospot (ELISpot). IFNy SFU/million PBMCs (Spot Forming Unit)

Time frame: 6 months

Population: For the H1N1 arm, there were only enough remaining PBMCs from 14 participants. For the H3N2 arm, there were insufficient cells to run the analysis. For the RSV arm, only 18/41 participants were analysed because there were insufficient PBMCs from the remaining participants to run the analysis.

ArmMeasureGroupValue (MEDIAN)
RSV A Memphis 37Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)Infected778.30 IFNy SFU/million PBMCs
RSV A Memphis 37Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)Uninfected159.20 IFNy SFU/million PBMCs
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)Infected161 IFNy SFU/million PBMCs
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Blood by Enzyme-linked Immunospot (ELISpot)Uninfected29 IFNy SFU/million PBMCs
Secondary

Frequency of T Cells in Blood by Flow Cytometry

Peak Ki-67+ CD38+ CD8+ T cells in the blood by flow cytometry.

Time frame: 6 months

Population: For the H1N1 arm, one participant was excluded from analysis as they had RSV co-infection.~For the RSV arm, only 32/41 participants were analysed because there were insufficient PBMCs from the remaining participants to run the analysis

ArmMeasureGroupValue (MEDIAN)
RSV A Memphis 37Frequency of T Cells in Blood by Flow CytometryInfected0.79 % of CD8+ lymphocytes
RSV A Memphis 37Frequency of T Cells in Blood by Flow CytometryUninfected0.49 % of CD8+ lymphocytes
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Blood by Flow CytometryInfected3.81 % of CD8+ lymphocytes
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Blood by Flow CytometryUninfected0.985 % of CD8+ lymphocytes
Influenza A/Belgium/4217/2015 (H3N2)Frequency of T Cells in Blood by Flow CytometryInfected4.13 % of CD8+ lymphocytes
Influenza A/Belgium/4217/2015 (H3N2)Frequency of T Cells in Blood by Flow CytometryUninfected1.18 % of CD8+ lymphocytes
Secondary

Frequency of T Cells in Respiratory Tract by Flow Cytometry

Peak Ki-67+ CD38+ CD8+ T cells in bronchoalveolar lavage (BAL) by flow cytometry

Time frame: 6 months

Population: For the H1N1 arm, one participant was excluded from analysis as they had RSV co-infection.~For the RSV arm, only 20/41 participants were analysed because there were insufficient airway cells from some participants to run the analysis.~For the H3N2 arm, the analysis was not run on the 3 uninfected participants. Only 3 were analysed in the infected participants because 1 participant was excluded for co-infection and the other 3 participants had insufficient airway cells to run the analysis.

ArmMeasureGroupValue (MEDIAN)
RSV A Memphis 37Frequency of T Cells in Respiratory Tract by Flow CytometryInfected2.21 % of CD8+ lymphocytes
RSV A Memphis 37Frequency of T Cells in Respiratory Tract by Flow CytometryUninfected0.65 % of CD8+ lymphocytes
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Respiratory Tract by Flow CytometryInfected81.15 % of CD8+ lymphocytes
Influenza A/California/04/2009-like (H1N1)Frequency of T Cells in Respiratory Tract by Flow CytometryUninfected0.412 % of CD8+ lymphocytes
Influenza A/Belgium/4217/2015 (H3N2)Frequency of T Cells in Respiratory Tract by Flow CytometryInfected4.36 % of CD8+ lymphocytes
Secondary

Viral Load

Nasal wash viral load by quantitative polymerase chain reaction (qPCR) (Area under curve)

Time frame: 28 days

Population: For the H1N1 arm, one participant was excluded from analysis as they had RSV co-infection.

ArmMeasureGroupValue (MEDIAN)
RSV A Memphis 37Viral LoadInfected18.24 log10 copies*days/mL
RSV A Memphis 37Viral LoadUninfected0 log10 copies*days/mL
Influenza A/California/04/2009-like (H1N1)Viral LoadInfected5.85 log10 copies*days/mL
Influenza A/California/04/2009-like (H1N1)Viral LoadUninfected0 log10 copies*days/mL
Influenza A/Belgium/4217/2015 (H3N2)Viral LoadInfected26.40 log10 copies*days/mL
Influenza A/Belgium/4217/2015 (H3N2)Viral LoadUninfected0 log10 copies*days/mL

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026