Innate Immune Responses and Rapid Control of Inflammation in African Green Monkeys Treated or Not with Interferon-Alpha during Primary SIVagm Infection
MESH: Antiviral Agents
MESH: Inflammation
[SDV.IMM] Life Sciences [q-bio]/Immunology
QH301-705.5
[SDV]Life Sciences [q-bio]
T-Lymphocytes
MESH: Simian Immunodeficiency Virus
Simian Acquired Immunodeficiency Syndrome
Lymphocyte Activation
[SDV.IMM.II]Life Sciences [q-bio]/Immunology/Innate immunity
Antiviral Agents
03 medical and health sciences
0302 clinical medicine
[SDV.MHEP.MI]Life Sciences [q-bio]/Human health and pathology/Infectious diseases
Chlorocebus aethiops
Animals
MESH: Animals
Biology (General)
MESH: Lymphocyte Activation
[SDV.IMM.II] Life Sciences [q-bio]/Immunology/Innate immunity
[SDV.MP.VIR] Life Sciences [q-bio]/Microbiology and Parasitology/Virology
Inflammation
MESH: Cytokines
Interferon-alpha
[SDV.IMM.IMM]Life Sciences [q-bio]/Immunology/Immunotherapy
RC581-607
MESH: Cercopithecus aethiops
MESH: Gene Expression Regulation
Immunity, Innate
3. Good health
[SDV] Life Sciences [q-bio]
MESH: T-Lymphocytes
Gene Expression Regulation
[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/Virology
[SDV.MHEP.MI] Life Sciences [q-bio]/Human health and pathology/Infectious diseases
[SDV.IMM]Life Sciences [q-bio]/Immunology
Cytokines
MESH: Immunity, Innate
Simian Immunodeficiency Virus
[SDV.IMM.IMM] Life Sciences [q-bio]/Immunology/Immunotherapy
MESH: Simian Acquired Immunodeficiency Syndrome
MESH: Interferon-alpha
Immunologic diseases. Allergy
Research Article
DOI:
10.1371/journal.ppat.1004241
Publication Date:
2014-07-03T18:13:21Z
AUTHORS (14)
ABSTRACT
Chronic immune activation (IA) is considered as the driving force of CD4+ T cell depletion and AIDS. Fundamental clues in mechanisms that regulate IA could lie natural hosts SIV, such African green monkeys (AGMs). Here we investigated role innate cells IFN-α control AGMs. AGMs displayed significant NK upon SIVagm infection, which was correlated with levels IFN-α. Moreover, detected cytotoxic lymph nodes during early acute phase infection. Both plasmacytoid myeloid dendritic (pDC mDC) homing receptors were increased, but maturation mDCs, particular CD16+ more important than pDCs. Monitoring 15 cytokines showed those, are known to be increased HIV-1/SIVmac pathogenic infections, IL-15, IFN-α, MCP-1 CXCL10/IP-10, significantly well. In contrast, generally induced later stage IL-6, IL-18 TNF-α, less or not suggesting an IA. We then treated daily high doses from day 9 24 post-infection. No impact observed on profiles pDCs cells. There also no major difference interferon-stimulated gene (ISG) expression sign disease progression. Thus, even after administration still able IA, showing independent levels. This suggests sustained ISG HIV/SIVmac infections involves non-IFN-α products.
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