Impaired Antibody-Independent Immune Response of B Cells in Patients With Acute Dengue Infection

Autor: Denis R. St. Laurent, Veasna Duong, Sothy Heng, Tineke Cantaert, Philippe Dussart, Sivlin Ung, Sowath Ly, Sopheak Sorn, Vinit Upasani, Hoa Thi My Vo, Izabela A. Rodenhuis-Zybert, Rithy Choeung
Přispěvatelé: Immunologie [Phnom Penh], Institut Pasteur du Cambodge, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP), University of Groningen [Groningen], University Medical Center Groningen [Groningen] (UMCG), Kantha Bopha Hospitals Foundation, Unité de Virologie / Virology Unit [Phnom Penh], Unité d'Épidémiologie et de Santé Publique [Phnom Penh], TC was funded by the Institute Pasteur International Network and is an HHMI-Wellcome Trust International Research Scholar (208710/Z/17/Z). VU was funded by the Institute Pasteur International Network Calmette and Yersin Ph.D. scholarship., Microbes in Health and Disease (MHD)
Jazyk: angličtina
Rok vydání: 2019
Předmět:
0301 basic medicine
Male
CD32
MESH: Interleukin-10
viruses
B cell subsets
LEVEL
MESH: Dengue
Dengue virus
CD38
medicine.disease_cause
Antibodies
Viral

MESH: Dengue Virus
DISEASE
Dengue fever
Dengue
0302 clinical medicine
immune system diseases
MESH: Child
Immunology and Allergy
Child
MESH: Antigens
CD

Original Research
B-Lymphocytes
biology
PLASMA
virus diseases
hemic and immune systems
3. Good health
Interleukin-10
RECEPTORS
medicine.anatomical_structure
Child
Preschool

Acute Disease
[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
IL-10
MESH: Acute Disease
[SDV.IMM]Life Sciences [q-bio]/Immunology
Female
immunopathogenesis of dengue
Antibody
ARTHRITIS
lcsh:Immunologic diseases. Allergy
Adolescent
Naive B cell
Immunology
chemical and pharmacologic phenomena
VIRUS-INFECTION
DENDRITIC CELLS
regulatory B cells (Bregs)
03 medical and health sciences
Immune system
Antigens
CD

MESH: B-Lymphocytes
medicine
Humans
B cell
MESH: Adolescent
MESH: Humans
dengue virus
plasmacells
IDENTIFICATION
business.industry
Tumor Necrosis Factor-alpha
MESH: Child
Preschool

medicine.disease
MESH: Male
030104 developmental biology
MESH: Tumor Necrosis Factor-alpha
IMMUNOGLOBULIN
biology.protein
lcsh:RC581-607
business
MESH: Female
MESH: Antibodies
Viral

DEPENDENT ENHANCEMENT
030215 immunology
Zdroj: Frontiers in Immunology
Frontiers in Immunology, Frontiers, 2019, 10, pp.2500. ⟨10.3389/fimmu.2019.02500⟩
Frontiers in Immunology, 10:2500. Frontiers Media SA
Frontiers in Immunology, Vol 10 (2019)
ISSN: 1664-3224
DOI: 10.3389/fimmu.2019.02500
Popis: Dengue is a mosquito-borne viral disease caused by dengue virus (DENV). The disease is endemic to more than 100 countries with 390 million dengue infections per year. Humoral immune responses during primary and secondary DENV infections are well-investigated. However, the impact of DENV infection on B cell subsets and their antibody-independent functions are not well-documented. Through this study, we aimed to define the distribution of B cell subsets in the acute phase of DENV infection and characterize the effect of DENV infection on B cell functions such as differentiation into memory and plasma cells and cytokine production. In our cohort of Cambodian children, we observed decreased percentages of CD24(hi)CD38(hi) B cells and CD27(-) naive B cells within the CD19 population and increased percentages of CD27(+)CD38(hi)CD138(+) plasma cells as early as 4 days post appearance of fever in patients with severe dengue compared to patients with mild disease. Lower percentages of CD19(+)CD24(hi)CD38(hi) B cells in DENV-infected patients were associated with decreased concentrations of soluble CD40L in patient plasma and decreased platelet counts in these patients. In addition, CD19(+)CD24(hi)CD38(hi) and CD19(+)CD27(-) B cells from DENV-infected patients did not produce IL-10 or TNF-alpha upon stimulation in vitro, suggesting their contribution to an altered immune response during DENV infection. In addition, CD19(+)CD27(-) naive B cells isolated from dengue patients were refractory to TLR/anti-IgM stimulation in vitro, which correlated to the increased expression of inhibitory Fc gamma receptors (Fc gamma R) CD32 and LILRB1 on CD19(+)CD27(-) naive B cells from DENV-infected patients. Collectively, our results indicate that a defective B cell response in dengue patients may contribute to the pathogenesis of dengue during the early phase of infection.
Databáze: OpenAIRE