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Challenge of the Nasopharynx With Neisseria Lactamica Expressing the Meningococcal Protein Neisseria Adhesin A (NadA) (NadA-Lac4)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03630250
Recruitment Status : Completed
First Posted : August 14, 2018
Last Update Posted : February 27, 2020
Sponsor:
Collaborator:
University Hospital Southampton NHS Foundation Trust
Information provided by (Responsible Party):
University of Southampton

Brief Summary:

This study is part of a research programme that aims to improve ways of protecting people from serious illnesses such as meningitis and sepsis caused by a bacterium called Neisseria meningitidis (N. meningitidis), using a closely related but harmless bacterium called Neisseria lactamica (N. lactamica). Investigators have previously given nose drops containing N. lactamica to over 350 volunteers - this is known as inoculation. In these studies the investigators have shown that they can cause colonisation of many inoculated volunteers (35-60%) with N. lactamica. Colonisation is when bacteria survive on or in a person without causing any illness or disease. N. lactamica specifically colonises the nose and throat. Investigators have also shown that colonisation with N. lactamica results in an immune (antibody) response.

In this study investigators will be using a genetically modified version of N. lactamica which contains a single gene from N. meningitides. It is anticipated that the presence of this gene will change the number of people who are colonised and how long people remain colonised for, as well as causing them to produce an immune response to N. meningitides.

The purpose of this study are to prove that inoculation with this modified N. lactamica does not cause any symptoms or illness, and to analyse the immune response produced in healthy volunteers.


Condition or disease Intervention/treatment Phase
Meningitis, Bacterial Neisseria Infection Biological: N. lactamica Early Phase 1

Detailed Description:
The NadA protein is one of the 4 strongly immunogenic components of the 4CMenB vaccine against serogroup B meningococcal disease (Bexsero) and has been demonstrated to be immunogenic in terms of generating serum bactericidal antibodies against N. meningitides strains that express the cognate NadA. Furthermore, University students vaccinated with Bexsero exhibit moderately reduced acquisition of nasopharyngeal carriage of N. meningitidis over the course of 12 months after vaccination. These studies imply that NadA expression by N. meningitidis may induce systemic and mucosal immunity to NadA during carriage, and that immunity directed against NadA may protect against colonisation by N. meningitidis. A greater understanding of the mucosal immune mechanisms of protection against pathobionts is essential for design of more effective and long lasting vaccines in the future. Then direct way to do this would be experimental human challenge with N. meningitidis but this carries potential hazard. As N. lactamica human challenge has shown to be safe, an alternative technique to investigate mucosal immunity to meningococcal antigens such as NadA will utilise Genetically Modified Organisms (GMOs) such as the one described here. Two strains of genetically modified N. lactamica will be used in this study, both of which have been derived from a beta-D-galactosidase (lacZ)-deficient mutant strain of N. lactamica Y92-1009 (△lacZ). This mutant can be differentiated from wild type bacteria when grown on the chromogenic substrate, X-gal. Both Genetically modified (GM) strains have demonstrated to remain acutely susceptible to killing by normal human serum and retain sensitivity to the front-line antibiotics used clinically to treat meningococcal disease (rifampicin, ciprofloxacin and ceftriaxone). The efficacy of ciprofloxacin to clear N. lactamica carriage is likely to similar as for N. meningitidis, as the organism is extremely sensitive to this antibiotic. Ciprofloxacin has been effective in clearing N. lactamica carriage within 24 hours in 100% of 4 individuals experimentally colonised in an ongoing human challenge study with wild type N. lactamica (unpublished data).

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 35 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Cohort
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Challenge of the Nasopharynx With Neisseria Lactamica Expressing the Meningococcal Protein Neisseria Adhesin A (NadA)
Actual Study Start Date : October 18, 2018
Actual Primary Completion Date : September 1, 2019
Actual Study Completion Date : September 1, 2019


Arm Intervention/treatment
Experimental: Challenge Volunteer - 4BN1

Volunteers will be given a choice of which version of the GM N. lactamica they would like to be given (4BN1 or 4YB2).

On Day 0 Challenge volunteers will be asked to lie on their back, 0.5 mL of fluid containing a carefully measured amount of 4BN1 will be dripped slowly into each nostril. The volunteer will be able to breathe through their mouth during the procedure. Volunteers will be asked to remain lying down for 15 minutes. This will be performed only once.

Volunteers will then be admitted to the NIHR Southampton CRF for 5 days. Challenge volunteers will then be asked to return for follow up visits on Day 7, 10, 14, 28, 56 90 & 92.

A single dose of an antibiotic (Ciprofloxacin) will be administered on day 90 regardless of colonisation with modified N. lactamica 4BN1.

Biological: N. lactamica
Genetically modified N. lactamica

No Intervention: Contact Volunteer
Contact volunteers are those volunteers whose partner/spouse is a Challenge volunteer. Investigators will monitor Contact volunteers to collect information about transmission. A single dose of an antibiotic (Ciprofloxacin) will be administered on Day 90 regardless of colonisation with modified N. lactamica.
Experimental: Challenge Volunteer - 4YB2

Volunteers will be given a choice of which version of the GM N. lactamica they would like to be given (4BN1 or 4YB2).

On Day 0 Challenge volunteers will be asked to lie on their back, 0.5 mL of fluid containing a carefully measured amount of 4YB2 will be dripped slowly into each nostril. The volunteer will be able to breathe through their mouth during the procedure. Volunteers will be asked to remain lying down for 15 minutes. This will be performed only once.

Volunteers will then be admitted to the NIHR Southampton CRF for 5 days. Challenge volunteers will then be asked to return for follow up visits on Day 7, 10, 14, 28, 56 90 & 92.

A single dose of an antibiotic (Ciprofloxacin) will be administered on day 90 regardless of colonisation with modified N. lactamica 4YB2

Biological: N. lactamica
Genetically modified N. lactamica




Primary Outcome Measures :
  1. Establish the effect of the nasal inoculation of healthy volunteers with a genetically modified strain of Neisseria lactamica expressing NadA by measuring respiratory rate. [ Time Frame: Up to volunteer visit Day 4 ]
    Volunteers are admitted to the NIHR Southampton CRF and closely observed by trained medical members for any potential effects. Respiratory rate (breaths per minute) will be measured and compared with baseline measurements. A consistent increase in respiratory rate could indicate ill health and potential disease. A study doctor will review each participant twice a day for the duration of the inpatient stay.

  2. Establish the effect of the nasal inoculation of healthy volunteers with a genetically modified strain of Neisseria lactamica expressing NadA by measuring body temperature. [ Time Frame: Up to volunteer visit Day 4 ]
    Volunteers are admitted to the NIHR Southampton CRF and closely observed by trained medical members for any potential effects. Body temperature (degrees Celsius) will be measured and compared with baseline measurements. A constant increase in body temperature could indicate ill health and potential disease. A study doctor will review each participant twice a day for the duration of the inpatient stay.

  3. Establish the effect of the nasal inoculation of healthy volunteers with a genetically modified strain of Neisseria lactamica expressing NadA by measuring heart rate. [ Time Frame: Up to volunteer visit Day 4 ]
    Volunteers are admitted to the NIHR Southampton CRF and closely observed by trained medical members for any potential effects. Heart rate (beats per minute) will be measured and compared with baseline measurements. An increase in heart rate could indicate ill health and potential disease. A study doctor will review each participant twice a day for the duration of the inpatient stay.

  4. Establish the effect of the nasal inoculation of healthy volunteers with a genetically modified strain of Neisseria lactamica expressing NadA by measuring blood pressure. [ Time Frame: Up to volunteer visit Day 4 ]
    Volunteers are admitted to the NIHR Southampton CRF and closely observed by trained medical members for any potential effects. Blood pressure (mmHg) will be measured and compared with baseline measurements. An increase in blood pressure could indicate ill health and potential disease. A study doctor will review each participant twice a day for the duration of the inpatient stay.


Secondary Outcome Measures :
  1. To measure the NadA specific immunity in healthy volunteers following nasal inoculation with Neisseria lactamica expressing NadA [ Time Frame: Up to volunteer visit Day 92 ]
    Colonisation by Neisseria lactamica has previously shown to elicit a mucosal antibody response. Saliva samples will be collected from volunteers and antibody levels (µg/mL) specific to NadA pre and post inoculation will be measured to confirm if there is an increase. Those volunteers successfully colonised are hypothesised to show an increase in antibody production.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

The challenge volunteer must satisfy all the following inclusion criteria to be eligible for the study:

  • Healthy adults aged 18 to 45 years inclusive on the day of enrolment
  • Fully conversant in the English language
  • Able and willing (in the investigator's opinion) to comply with all study requirements
  • Provide written informed consent to participate in the trial
  • Provide written agreement to abide by infection control guidelines including agreement to abstain from intimate contact with any individual other than one declared and consented bedroom contact during the study period
  • Provide written consent to allow the study team to discuss the volunteer's medical history with the General Practitioner
  • Written informed contact volunteer consent provided by any bedroom contact
  • Agreement to be admitted to Southampton NIHR-CRF for 4.5 days following inoculation
  • For females only, willingness to practice continuous effective contraception (see below) during the study and a negative pregnancy test on the day(s) of screening and inoculation
  • Able to correctly answer all questions in the pre-consent and infection control questionnaires
  • Agreement to take antibiotic eradication therapy according to the study protocol
  • TOPS registration completed and no conflict found

Exclusion Criteria:

The challenge volunteer may not enter the study if any of the following criteria apply:

  • Current active smokers defined as having smoked a cigarette or cigar in the last four weeks
  • N. lactamica or N. meningitidis detected on throat swab or nasal wash taken at screening or at the pre-challenge visit
  • Individuals who have a current infection at the time of inoculation
  • Individuals who have been involved in other clinical trials involving receipt of an investigational product over the last 12 weeks or if there is planned use of an investigational product during the study period
  • Individuals who have previously been involved in clinical trials investigating meningococcal vaccines or experimental challenge with N. lactamica
  • Individuals who have received one or more doses of the meningococcus B vaccine Bexsero
  • Use of systemic antibiotics within the period 30 days prior to the challenge
  • Any confirmed or suspected immunosuppressive or immune-deficient state, including HIV infection; malignancy, asplenia; recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (topical steroids are allowed)
  • Use of immunoglobulins or blood products within 3 months prior to enrolment.
  • History of allergic disease or reactions likely to be exacerbated by any component of the inoculum
  • Contraindications to the use of ciprofloxacin, specifically a history of epilepsy, prolonged QT interval, hypersensitivity to quinolones or a history of tendon disorders related to quinolone use
  • Contraindications to the use of ceftriaxone, specifically hypersensitivity to any cephalosporins
  • Any clinically significant abnormal finding on clinical examination or screening investigations. In the event of abnormal test results, confirmatory repeat tests will be requested.
  • Any other significant disease, disorder, or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data, for example recent surgery to the nasopharynx
  • Occupational, household or intimate contact with immunosuppressed persons, specifically HIV infection with a CD4 count <200 cells/mm3; asplenia; any malignancy, recurrent, severe infections and chronic (more than 14 days) immunosuppressant medication within the past 6 months (topical steroids are allowed)
  • Occupational or household contact with children under 5 years or an older child with a tendency to co-sleep with the volunteer
  • Pregnancy, lactation or intention to become pregnant during the study
  • Inability of the study team to contact the volunteer's GP to confirm medical history and safety to participate

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03630250


Locations
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United Kingdom
NIHR Southampton Clinical Research Facility
Southampton, United Kingdom
Sponsors and Collaborators
University of Southampton
University Hospital Southampton NHS Foundation Trust
Investigators
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Principal Investigator: Robert C Read University of Southampton
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: University of Southampton
ClinicalTrials.gov Identifier: NCT03630250    
Other Study ID Numbers: NadA-Lac4
First Posted: August 14, 2018    Key Record Dates
Last Update Posted: February 27, 2020
Last Verified: February 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University of Southampton:
meningitis
GMO
Additional relevant MeSH terms:
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Meningococcal Infections
Meningitis, Bacterial
Meningitis
Central Nervous System Diseases
Nervous System Diseases
Neisseriaceae Infections
Gram-Negative Bacterial Infections
Bacterial Infections
Central Nervous System Bacterial Infections
Central Nervous System Infections