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Increased adaptive immune responses and proper feedback regulation protect against clinical dengue
- Source :
- Science Translational Medicine, Science Translational Medicine, American Association for the Advancement of Science, 2017, 9 (405), pp.eaal5088. ⟨10.1126/scitranslmed.aal5088⟩, Science Translational Medicine, 2017, 9 (405), pp.eaal5088. ⟨10.1126/scitranslmed.aal5088⟩, Science Translational Medicine, American Association for the Advancement of Science, 2017, 9 (405), 〈10.1126/scitranslmed.aal5088〉
- Publication Year :
- 2017
- Publisher :
- HAL CCSD, 2017.
-
Abstract
- International audience; Clinical symptoms of dengue virus (DENV) infection, the most prevalent arthropod-borne viral disease, range from classical mild dengue fever to severe, life-threatening dengue shock syndrome. However, most DENV infections cause few or no symptoms. Asymptomatic DENV-infected patients provide a unique opportunity to decipher the host immune responses leading to virus elimination without negative impact on an individual's health. We used an integrated approach of transcriptional profiling and immunological analysis to compare a Cambodian population of strictly asymptomatic viremic individuals with clinical dengue patients. Whereas inflammatory pathways and innate immune response pathways were similar between asymptomatic individuals and clinical dengue patients, expression of proteins related to antigen presentation and subsequent T cell and B cell activation pathways was differentially regulated, independent of viral load and previous DENV infection history. Feedback mechanisms controlled the immune response in asymptomatic viremic individuals, as demonstrated by increased activation of T cell apoptosis-related pathways and FcγRIIB (Fcγ receptor IIB) signaling associated with decreased anti-DENV-specific antibody concentrations. Together, our data illustrate that symptom-free DENV infection in children is associated with increased activation of the adaptive immune compartment and proper control mechanisms, leading to elimination of viral infection without excessive immune activation, with implications for novel vaccine development strategies.
- Subjects :
- 0301 basic medicine
MESH: Inflammation
Transcription, Genetic
MESH: Feedback, Physiological
T-Lymphocytes
viruses
Apoptosis
MESH: Dengue
Adaptive Immunity
Dengue virus
Antibodies, Viral
Lymphocyte Activation
medicine.disease_cause
Dengue fever
Dengue
0302 clinical medicine
[STAT.ML]Statistics [stat]/Machine Learning [stat.ML]
MESH: Demography
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
MESH: Child
[ SDV.IMM ] Life Sciences [q-bio]/Immunology
Child
MESH: Treatment Outcome
Feedback, Physiological
Antigen Presentation
education.field_of_study
MESH: Cytokines
MESH: Plasma Cells
Cell Differentiation
General Medicine
Viral Load
MESH: Gene Expression Regulation
3. Good health
[ SDV.MHEP.MI ] Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Treatment Outcome
medicine.anatomical_structure
[SDV.IMM.IA]Life Sciences [q-bio]/Immunology/Adaptive immunology
Acute Disease
Cytokines
MESH: Acute Disease
MESH: Immunity, Innate
medicine.symptom
MESH: Viral Load
Viral load
MESH: Cell Differentiation
T cell
Plasma Cells
030231 tropical medicine
Population
Asymptomatic
03 medical and health sciences
Immune system
medicine
Humans
Viremia
MESH: Viremia
Quantitative Biology - Populations and Evolution
education
MESH: Lymphocyte Activation
Demography
Inflammation
Innate immune system
MESH: Humans
[ SDV ] Life Sciences [q-bio]
business.industry
MESH: Transcription, Genetic
MESH: Apoptosis
Populations and Evolution (q-bio.PE)
biochemical phenomena, metabolism, and nutrition
medicine.disease
Immunity, Innate
030104 developmental biology
MESH: T-Lymphocytes
Gene Expression Regulation
FOS: Biological sciences
Immunology
MESH: Antigen Presentation
business
MESH: Adaptive Immunity
MESH: Antibodies, Viral
Subjects
Details
- Language :
- English
- ISSN :
- 19466234 and 19466242
- Database :
- OpenAIRE
- Journal :
- Science Translational Medicine, Science Translational Medicine, American Association for the Advancement of Science, 2017, 9 (405), pp.eaal5088. ⟨10.1126/scitranslmed.aal5088⟩, Science Translational Medicine, 2017, 9 (405), pp.eaal5088. ⟨10.1126/scitranslmed.aal5088⟩, Science Translational Medicine, American Association for the Advancement of Science, 2017, 9 (405), 〈10.1126/scitranslmed.aal5088〉
- Accession number :
- edsair.doi.dedup.....904c1432a4d502f69cdbd45e5d6851f5