Ignite Creation Date:
2025-12-25 @ 4:05 AM
Ignite Modification Date:
2025-12-30 @ 5:45 AM
Study NCT ID:
NCT01707602
Status:
COMPLETED
Last Update Posted:
2013-08-05
First Post:
2012-10-12
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Routes of Immunization and Flu Immune Responses
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D007251', 'term': 'Influenza, Human'}], 'ancestors': [{'id': 'D012141', 'term': 'Respiratory Tract Infections'}, {'id': 'D007239', 'term': 'Infections'}, {'id': 'D009976', 'term': 'Orthomyxoviridae Infections'}, {'id': 'D012327', 'term': 'RNA Virus Infections'}, {'id': 'D014777', 'term': 'Virus Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C478242', 'term': 'vaxigrip'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 60}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2012-10'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2013-07', 'completionDateStruct': {'date': '2013-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2013-08-02', 'studyFirstSubmitDate': '2012-10-12', 'studyFirstSubmitQcDate': '2012-10-15', 'lastUpdatePostDateStruct': {'date': '2013-08-05', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2012-10-16', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2012-12', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'CD8 T cell responses', 'timeFrame': '21 days', 'description': 'CD8 T cell responses against the specific vaccine strain will be measured at baseline and day 21 after vaccination by flow cytometry. Secretion of cytokines measured by intracellular staining will be compared between TC, ID and IM routes of vaccination.'}], 'secondaryOutcomes': [{'measure': 'Safety', 'timeFrame': '5 months', 'description': 'Safety will be assessed at each visit by recording clinical local and systemic tolerance including reporting of adverse events. Frequency and severity of local and systemic adverse events following vaccination will be compared between TC, ID and IM vaccination groups.'}, {'measure': 'Haemagglutination Inhibition', 'timeFrame': '5 months', 'description': 'Haemagglutination Inhibition and microneutralization assays will be performed at day0, day 21 and month 5 after vaccination to define the humoral response against a vaccine-homologous virus that meets or exceeds the EMEA (CHMP) guidance targets for influenza vaccine seroconversion rate (SCR), seroprotection rate (SPR), and geometric mean fold rise (GMFR).'}, {'measure': 'CD4 T cell responses', 'timeFrame': '21 days', 'description': 'CD4 T cell responses against the specific vaccine strain will be measured at baseline and day 21 by intracellular staining and flow cytometry. Effector CD4 T cell responses will be compared between TC, ID and IM vaccination groups.'}, {'measure': 'Memory CD8 and CD4 T cell responses', 'timeFrame': '5 months', 'description': 'Memory CD8 and CD4 T cell responses against the specific vaccine strain will be assessed by flow cytometry 5 month after vaccination by TC, ID and IM routes.'}, {'measure': 'Inflammation', 'timeFrame': '1 day', 'description': 'Inflammation and systemic innate immune response will be assessed on day 1 after vaccination (compared with the basal inflammatory status) by studying the transcriptional profile of blood cells (microarrays) and inflammatory cytokines dosage in the serum.'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['Intradermal', 'transcutaneous', 'influenza', 'routes of vaccination', 'T cell responses', 'humoral responses', 'skin', 'clinical trial', 'Novel application of influenza vaccine', 'Transcutaneous vaccination(hair follicular targeting)', 'Intradermal vaccination(micro-needle)'], 'conditions': ['Influenza']}, 'referencesModule': {'references': [{'pmid': '20303671', 'type': 'BACKGROUND', 'citation': 'Combadiere B, Siberil S, Duffy D. Keeping the memory of influenza viruses. Pathol Biol (Paris). 2010 Apr;58(2):e79-86. doi: 10.1016/j.patbio.2010.01.010. Epub 2010 Mar 19.'}, {'pmid': '593371', 'type': 'BACKGROUND', 'citation': 'McMichael AJ, Ting A, Zweerink HJ, Askonas BA. HLA restriction of cell-mediated lysis of influenza virus-infected human cells. Nature. 1977 Dec 8;270(5637):524-6. doi: 10.1038/270524a0. No abstract available.'}, {'pmid': '20520820', 'type': 'BACKGROUND', 'citation': 'Combadiere B, Vogt A, Mahe B, Costagliola D, Hadam S, Bonduelle O, Sterry W, Staszewski S, Schaefer H, van der Werf S, Katlama C, Autran B, Blume-Peytavi U. Preferential amplification of CD8 effector-T cells after transcutaneous application of an inactivated influenza vaccine: a randomized phase I trial. PLoS One. 2010 May 26;5(5):e10818. doi: 10.1371/journal.pone.0010818.'}, {'pmid': '21817854', 'type': 'BACKGROUND', 'citation': 'Combadiere B, Liard C. Transcutaneous and intradermal vaccination. Hum Vaccin. 2011 Aug;7(8):811-27. doi: 10.4161/hv.7.8.16274. Epub 2011 Aug 1.'}, {'pmid': '18486285', 'type': 'BACKGROUND', 'citation': 'Lambert PH, Laurent PE. Intradermal vaccine delivery: will new delivery systems transform vaccine administration? Vaccine. 2008 Jun 19;26(26):3197-208. doi: 10.1016/j.vaccine.2008.03.095. Epub 2008 Apr 22.'}, {'pmid': '16614727', 'type': 'BACKGROUND', 'citation': 'Vogt A, Combadiere B, Hadam S, Stieler KM, Lademann J, Schaefer H, Autran B, Sterry W, Blume-Peytavi U. 40 nm, but not 750 or 1,500 nm, nanoparticles enter epidermal CD1a+ cells after transcutaneous application on human skin. J Invest Dermatol. 2006 Jun;126(6):1316-22. doi: 10.1038/sj.jid.5700226.'}, {'pmid': '18209043', 'type': 'BACKGROUND', 'citation': 'Vogt A, Mahe B, Costagliola D, Bonduelle O, Hadam S, Schaefer G, Schaefer H, Katlama C, Sterry W, Autran B, Blume-Peytavi U, Combadiere B. Transcutaneous anti-influenza vaccination promotes both CD4 and CD8 T cell immune responses in humans. J Immunol. 2008 Feb 1;180(3):1482-9. doi: 10.4049/jimmunol.180.3.1482.'}, {'pmid': '19052565', 'type': 'BACKGROUND', 'citation': 'Mahe B, Vogt A, Liard C, Duffy D, Abadie V, Bonduelle O, Boissonnas A, Sterry W, Verrier B, Blume-Peytavi U, Combadiere B. Nanoparticle-based targeting of vaccine compounds to skin antigen-presenting cells by hair follicles and their transport in mice. J Invest Dermatol. 2009 May;129(5):1156-64. doi: 10.1038/jid.2008.356. Epub 2008 Dec 4.'}, {'pmid': '21554912', 'type': 'BACKGROUND', 'citation': 'Liard C, Munier S, Arias M, Joulin-Giet A, Bonduelle O, Duffy D, Shattock RJ, Verrier B, Combadiere B. Targeting of HIV-p24 particle-based vaccine into differential skin layers induces distinct arms of the immune responses. Vaccine. 2011 Aug 26;29(37):6379-91. doi: 10.1016/j.vaccine.2011.04.080. Epub 2011 May 7.'}, {'pmid': '22170490', 'type': 'BACKGROUND', 'citation': 'Liard C, Munier S, Joulin-Giet A, Bonduelle O, Hadam S, Duffy D, Vogt A, Verrier B, Combadiere B. Intradermal immunization triggers epidermal Langerhans cell mobilization required for CD8 T-cell immune responses. J Invest Dermatol. 2012 Mar;132(3 Pt 1):615-25. doi: 10.1038/jid.2011.346. Epub 2011 Dec 15.'}, {'pmid': '30843873', 'type': 'DERIVED', 'citation': 'Goncalves E, Bonduelle O, Soria A, Loulergue P, Rousseau A, Cachanado M, Bonnabau H, Thiebaut R, Tchitchek N, Behillil S, van der Werf S, Vogt A, Simon T, Launay O, Combadiere B. Innate gene signature distinguishes humoral versus cytotoxic responses to influenza vaccination. J Clin Invest. 2019 Mar 7;129(5):1960-1971. doi: 10.1172/JCI125372. Print 2019 May 1.'}]}, 'descriptionModule': {'briefSummary': 'The project aims to evaluate the impact of skin routes of immunization (transcutaneous and intradermal vs intramuscular) on cellular and humoral responses to seasonal influenza vaccination in adults (18-45 years old).', 'detailedDescription': 'New approaches addressing intradermal (ID) and transcutaneous (TC) routes of immunization have been developed over the past few years and have brought novel insight in quality and efficacy of the immune response. Indeed, compared to the muscular tissue widely used for vaccination, the skin is particularly rich in antigen presenting cells. Our recent works show that penetration of vaccine compounds into the hair follicular ducts surrounded by Langerhans cells induces potent cellular immunity in contrast to the intra-muscular immunization. Our results also suggest that differential targeting of epidermal Langerhans cells (by TC route) or dermal dendritic cells (by ID route) could modulate the intensity and quality of the immune response to vaccine.\n\nThe aim of this study is to evaluate the immune response to a seasonal influenza vaccine when administrated byTC (hair follicular targeting needle-free method), ID (micro-needle injection) and IM (conventional intramuscular injection) routes of immunization. Along with our previous pre-clinical and clinical studies, here we hypothesize that differential targeting of epidermis or dermis antigen-presenting cells will have a differential impact on the cellular and humoral immune responses to Influenza vaccine.\n\nObjectives:\n\nWe will conduct a phase I/II clinical trials on 60 healthy volunteers to compare TC and ID routes of immunization to the conventional intramuscular (IM) vaccination. The impact of these routes on cellular and humoral immune responses to seasonal influenza vaccine will be assessed at baseline, day 21 (effector phase) and month 5 (memory phase) after vaccination.\n\nOutcomes:\n\nUsing the seasonal Influenza vaccine as an example of conventional vaccine, this study will evaluate and compare the efficacy ofTC, ID and IMroutes of immunization to induce cellular responses at day 21 and memory responses at month 5 phases. The generation and maintenance of Flu specific and neutralizing antibodies will be measured by Haemagglutination Inhibition and microneutralization assays.Moreover, safety and tolerance to each vaccination methods will be evaluated as well as inflammation and innate immune response induced at day 1 after vaccination.\n\nAddressing innovative skin routes of immunization, this study represents an essential step to move forward in the development of new vaccination strategies. These results will have an important impact on the amelioration of vaccine efficacy and less invasive method of immunization.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '45 Years', 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Healthy volunteers, age between 18 and 45 years,\n* BMI between 21 - 26,\n* Phototype I to IV,\n* Subjects able to receive vaccine administration by any of the three administration routes,\n* Signature of the written informed consent,\n* Affiliated to a health social security system,\n\nExclusion Criteria:\n\n* Known pregnancy or positive urine pregnancy test for women of child-bearing age,\n* Known infection with HIV or/and HCV or/and HBV (AgHBs+),\n* Known or suspected immune dysfunction that is caused by a medical condition, or any other Cause,\n* Use, within the past 3 months, of any topical and systemic treatment that would interfere with assessment and/or investigational treatment (anti-inflammatory drugs, immunosuppressors or any immune modulator agent),\n* Use of any topical treatment on the injection site within the last four weeks,\n* Excessive terminal hair growth on the two investigational skin areas used for the transcutaneous mode of vaccination,\n* Phototype V-VI,\n* Any allergy or hypersensibility to one of the components of the Investigational Product,\n* Medical history of allergy or hypersensitization to any ingredient of colorant used in the transcutaneous mode of administration,\n* Administration of a live vaccine(≤ 28 days) or inactivated (≤ 14 days) or planned vaccination within 3months of inclusion (D0),\n* Medical history of skin cancer,\n* Any acute skin affection which may interfere with the trial assessment on the injection site,\n* Any acute or chronic infectious which may interfere with the trial assessment four weeks prior to enrolment,\n* Prevision of UV sessions or sun exposure 6 weeks prior to the study or during the study period,\n* Febrile illness(at least 37.5°Cmeasuredorally), any acute infectious event within one week prior to enrolment,\n* Flu confirmed by the presence of fever≥38.5°Cassociated with respiratory symptoms\n* History of GuillainBarre syndrome or brachial neuritis following a previous vaccination.\n* Participation in an other biomedical research during the study period or period of exclusion when inclusion\n* Subject being in the exclusion period of a previous clinical trial,'}, 'identificationModule': {'nctId': 'NCT01707602', 'acronym': 'FLUWAY', 'briefTitle': 'Routes of Immunization and Flu Immune Responses', 'organization': {'class': 'OTHER', 'fullName': 'Assistance Publique - Hôpitaux de Paris'}, 'officialTitle': 'Impact of Immunization Routes on the Immune Response to Influenza Vaccine', 'orgStudyIdInfo': {'id': 'P120201'}, 'secondaryIdInfos': [{'id': '2012-001967-55', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Arm A', 'description': 'Type Vaccine Name: INTANZA® 15 T Description : transcutaneous vaccination', 'interventionNames': ['Biological: INTANZA® 15 T']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Arm B', 'description': 'Type: Vaccine Name: INTANZA® 15ug Description : intradermal vaccination', 'interventionNames': ['Biological: INTANZA® 15']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Arm C', 'description': 'Type : Vaccine Name: Vaxigrip® Description :Intramuscular vaccination', 'interventionNames': ['Biological: Vaxigrip®']}], 'interventions': [{'name': 'INTANZA® 15', 'type': 'BIOLOGICAL', 'description': 'intradermal vaccination', 'armGroupLabels': ['Arm B']}, {'name': 'Vaxigrip®', 'type': 'BIOLOGICAL', 'description': 'Intramuscular vaccination', 'armGroupLabels': ['Arm C']}, {'name': 'INTANZA® 15 T', 'type': 'BIOLOGICAL', 'description': 'transcutaneous vaccination', 'armGroupLabels': ['Arm A']}]}, 'contactsLocationsModule': {'locations': [{'zip': '75679', 'city': 'Paris', 'country': 'France', 'facility': 'GH Cochin - Broca - Hôtel-Dieu CIC BT505', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}], 'overallOfficials': [{'name': 'Odile LAUNAY, M.D. Ph. D', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Assistance Publique - Hôpitaux de Paris'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Assistance Publique - Hôpitaux de Paris', 'class': 'OTHER'}, 'collaborators': [{'name': 'Institut National de la Santé Et de la Recherche Médicale, France', 'class': 'OTHER_GOV'}], 'responsibleParty': {'type': 'SPONSOR'}}}}