Candida albicans Infection Affords Protection against Reinfection via Functional Reprogramming of Monocytes

Autor: Bart Jan Kullberg, Evangelos J. Giamarellos-Bourboulis, Daniela C. Ifrim, Liesbeth Jacobs, Jessica Quintin, Leo A. B. Joosten, Mihai G. Netea, Cisca Wijmenga, Hendrik G. Stunnenberg, Jos W. M. van der Meer, Sadia Saeed, Joost H.A. Martens, Ramnik J. Xavier, Colin Logie, Trees Jansen
Přispěvatelé: Radboud University Medical Center [Nijmegen], Radboud university [Nijmegen], National and Kapodistrian University of Athens (NKUA), Jena University Hospital [Jena], University Medical Center Groningen [Groningen] (UMCG), Massachusetts General Hospital [Boston], Broad Institute of MIT and Harvard (BROAD INSTITUTE), Harvard Medical School [Boston] (HMS)-Massachusetts Institute of Technology (MIT)-Massachusetts General Hospital [Boston], Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Cancer Research
POLARIZATION
Genetics and epigenetic pathways of disease [NCMLS 6]
[SDV]Life Sciences [q-bio]
MESH: Monocytes
[SDV.IMM.II]Life Sciences [q-bio]/Immunology/Innate immunity
Monocytes
ACTIVATION
Mice
NATURAL-KILLER-CELLS
0302 clinical medicine
Candida albicans
IMMUNE-RESPONSE
MESH: Animals
TRANSCRIPTION
EPIGENETIC REGULATION
Cells
Cultured

[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/Mycology
0303 health sciences
MESH: Cytokines
IMMUNOSUPPRESSION
Candidiasis
Health aging / healthy living Pathogenesis and modulation of inflammation [IGMD 5]
Corpus albicans
MESH: Candidiasis
CROHNS-DISEASE
3. Good health
Pathogenesis and modulation of inflammation [N4i 1]
medicine.anatomical_structure
[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology
030220 oncology & carcinogenesis
Cytokines
[SDV.IMM]Life Sciences [q-bio]/Immunology
Female
Reprogramming
MESH: Cells
Cultured

Biology
Invasive mycoses and compromised host Infection and autoimmunity [N4i 2]
Microbiology
DENDRITIC CELLS
Article
03 medical and health sciences
Immune system
Immunity
MESH: Mice
Inbred C57BL

Virology
Immunology and Microbiology(all)
medicine
Animals
Humans
Lectins
C-Type

MESH: Mice
Molecular Biology
B cell
030304 developmental biology
Innate immune system
MESH: Humans
Monocyte
MESH: Candida albicans
MEMORY
Pathogenesis and modulation of inflammation Infection and autoimmunity [N4i 1]
biology.organism_classification
Mice
Inbred C57BL

Proto-Oncogene Proteins c-raf
Immunology
MESH: Proto-Oncogene Proteins c-raf
Parasitology
MESH: Female
MESH: Lectins
C-Type
Zdroj: Cell Host & Microbe, 12, 2, pp. 223-232
Cell Host and Microbe
Cell Host and Microbe, Elsevier, 2012, 12 (2), pp.223-232. ⟨10.1016/j.chom.2012.06.006⟩
Cell Host & Microbe, 12, 223-232
Cell Host & Microbe, 12(2), 223-232. CELL PRESS
ISSN: 1934-6069
1931-3128
DOI: 10.1016/j.chom.2012.06.006
Popis: Item does not contain fulltext Immunological memory in vertebrates is often exclusively attributed to T and B cell function. Recently it was proposed that the enhanced and sustained innate immune responses following initial infectious exposure may also afford protection against reinfection. Testing this concept of "trained immunity," we show that mice lacking functional T and B lymphocytes are protected against reinfection with Candida albicans in a monocyte-dependent manner. C. albicans and fungal cell wall beta-glucans induced functional reprogramming of monocytes, leading to enhanced cytokine production in vivo and in vitro. The training required the beta-glucan receptor dectin-1 and the noncanonical Raf-1 pathway. Monocyte training by beta-glucans was associated with stable changes in histone trimethylation at H3K4, which suggests the involvement of epigenetic mechanisms in this phenomenon. The functional reprogramming of monocytes, reminiscent of similar NK cell properties, supports the concept of "trained immunity" and may be employed for the design of improved vaccination strategies.
Databáze: OpenAIRE