Characterization of the cell-mediated immune response to Takeda's live-attenuated tetravalent dengue vaccine in adolescents participating in a phase 2 randomized controlled trial conducted in a dengue-endemic setting. Issue 8 (16th February 2022)
- Record Type:
- Journal Article
- Title:
- Characterization of the cell-mediated immune response to Takeda's live-attenuated tetravalent dengue vaccine in adolescents participating in a phase 2 randomized controlled trial conducted in a dengue-endemic setting. Issue 8 (16th February 2022)
- Main Title:
- Characterization of the cell-mediated immune response to Takeda's live-attenuated tetravalent dengue vaccine in adolescents participating in a phase 2 randomized controlled trial conducted in a dengue-endemic setting
- Authors:
- Tricou, Vianney
Gottardo, Raphael
Egan, Michael A.
Clement, Frédéric
Leroux-Roels, Geert
Sáez-Llorens, Xavier
Borkowski, Astrid
Wallace, Derek
Dean, Hansi J. - Abstract:
- Highlights: We characterized the T-cell responses elicited by TAK-003 against DENV non-structural proteins. Observed CD4+ and CD8+ T-cell responses were cross-reactive and multi-functional. Responses were observed irrespective of pre-vaccination DENV neutralizing antibodies. CD8+ responses were of greater magnitude than the CD4+ responses. Abstract: Background: As robust dengue-specific CD4+ and CD8+ T cell responses are essential for protective immunity, we assessed cell-mediated immune (CMI) responses to a DENV-2-based dengue tetravalent vaccine candidate (TAK-003) in adolescents living in Panama, a dengue-endemic country. Methods: Peripheral blood mononuclear cells were collected from a subset of 67 participants ≥ 10 years old included in a phase 2 clinical trial of TAK-003 (Clinicaltrials.gov: NCT02302066). Following stimulation with dengue peptides, the frequency, magnitude, and cross-reactivity of the CD8+ and CD4+ T cell IFN-γ, TNF-α and IL-2 responses were assessed by flow cytometry. Results: Intracellular cytokine staining identified NS1, NS3, and NS5 as the most common non-structural (NS) targets of the CD4+ T-cell response (IFN-γ+); NS3 and NS5 were the main NS targets of the CD8+ T cell response (IFN-γ+). Both CD4+ and CD8+ T-cell responses were multi-functional (IFN-γ + TNF-α + IL-2+) and cross-reactive against DENV-1, -3, and -4 serotypes. Similar responses were seen in all CMI assessments irrespective of participant baseline status for dengue neutralizingHighlights: We characterized the T-cell responses elicited by TAK-003 against DENV non-structural proteins. Observed CD4+ and CD8+ T-cell responses were cross-reactive and multi-functional. Responses were observed irrespective of pre-vaccination DENV neutralizing antibodies. CD8+ responses were of greater magnitude than the CD4+ responses. Abstract: Background: As robust dengue-specific CD4+ and CD8+ T cell responses are essential for protective immunity, we assessed cell-mediated immune (CMI) responses to a DENV-2-based dengue tetravalent vaccine candidate (TAK-003) in adolescents living in Panama, a dengue-endemic country. Methods: Peripheral blood mononuclear cells were collected from a subset of 67 participants ≥ 10 years old included in a phase 2 clinical trial of TAK-003 (Clinicaltrials.gov: NCT02302066). Following stimulation with dengue peptides, the frequency, magnitude, and cross-reactivity of the CD8+ and CD4+ T cell IFN-γ, TNF-α and IL-2 responses were assessed by flow cytometry. Results: Intracellular cytokine staining identified NS1, NS3, and NS5 as the most common non-structural (NS) targets of the CD4+ T-cell response (IFN-γ+); NS3 and NS5 were the main NS targets of the CD8+ T cell response (IFN-γ+). Both CD4+ and CD8+ T-cell responses were multi-functional (IFN-γ + TNF-α + IL-2+) and cross-reactive against DENV-1, -3, and -4 serotypes. Similar responses were seen in all CMI assessments irrespective of participant baseline status for dengue neutralizing antibodies and T cells. Conclusions: TAK-003 elicited cross-reactive, multi-functional CD4+ and CD8+ T-cell responses, irrespective of dengue pre-exposure. … (more)
- Is Part Of:
- Vaccine. Volume 40:Issue 8(2022)
- Journal:
- Vaccine
- Issue:
- Volume 40:Issue 8(2022)
- Issue Display:
- Volume 40, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 40
- Issue:
- 8
- Issue Sort Value:
- 2022-0040-0008-0000
- Page Start:
- 1143
- Page End:
- 1151
- Publication Date:
- 2022-02-16
- Subjects:
- Dengue vaccine -- Cell-mediated immunity -- Cytokine -- Seronegative -- Cross-reactive
Vaccines -- Periodicals
615.372 - Journal URLs:
- http://www.sciencedirect.com/science/journal/0264410X ↗
http://www.clinicalkey.com/dura/browse/journalIssue/0264410X ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/0264410X ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.vaccine.2022.01.016 ↗
- Languages:
- English
- ISSNs:
- 0264-410X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9138.628000
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British Library HMNTS - ELD Digital store - Ingest File:
- 20690.xml