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
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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