81 research outputs found

    An in vitro model to assess the immunosuppressive effect of tick saliva on the mobilization of inflammatory monocyte-derived cells

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    Tick-borne pathogens cause potent infections. These pathogens benefit from molecules contained in tick saliva that have evolved to modulate host innate and adaptive immune responses. This is called "saliva-activated transmission" and enables tick-borne pathogens to evade host immune responses. Ticks feed on their host for relatively long periods; thus, mechanisms counteracting the inflammation-driven recruitment and activation of innate effector cells at the bite site, are an effective strategy to escape the immune response. Here, we developed an original in vitro model to evaluate and to characterize the immunomodulatory effects of tick saliva that prevent the establishment of a local inflammatory immune response. This model mimics the tick bite and enables the assessment of the effect of saliva on the inflammatory-associated dynamic recruitment of cells from the mononuclear phagocyte system. Using this model, we were able to recapitulate the dual effect of tick saliva on the mobilization of inflammatory monocyte-derived cells, i.e. (i) impaired recruitment of monocytes from the blood to the bite wound; and (ii) poor mobilization of monocyte-derived cells from the skin to the draining lymph node. This simple tool reconstitutes the effect of tick saliva in vivo, which we characterized in the mouse, and should enable the identification of important factors facilitating pathogen infection. Furthermore, this model may be applied to the characterization of any pathogen-derived immunosuppressive molecule affecting the establishment of the inflammatory immune response

    Barrier Tissue Macrophages: Functional Adaptation to Environmental Challenges

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    Macrophages are found throughout the body, where they have crucial roles in tissue development, homeostasis and remodeling, as well as being sentinels of the innate immune system that can contribute to protective immunity and inflammation. Barrier tissues, such as the intestine, lung, skin and liver, are exposed constantly to the outside world, which places special demands on resident cell populations such as macrophages. Here we review the mounting evidence that although macrophages in different barrier tissues may be derived from distinct progenitors, their highly specific properties are shaped by the local environment, which allows them to adapt precisely to the needs of their anatomical niche. We discuss the properties of macrophages in steady-state barrier tissues, outline the factors that shape their differentiation and behavior and describe how macrophages change during protective immunity and inflammation

    Microneedle delivery of autoantigen for immunotherapy in type 1 diabetes

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    Antigen specific immunotherapy mediated via the sustained generation of regulatory T cells arguably represents the ideal therapeutic approach to preventing beta cell destruction in type 1 diabetes. However, there is a need to enhance the efficacy of this approach to achieve disease modification in man. Previous studies suggest that prolonged expression of self-antigen in skin in a non-inflammatory context is beneficial for tolerance induction. We therefore sought to develop a dry-coated microneedle (MN) delivery system and combine it with topical steroid to minimise local inflammation and promote prolonged antigen presentation in the skin. Here we show that a combination of surface-modified MNs coated with appropriate solvent systems can deliver therapeutically relevant quantities of peptide to mouse and human skin even with hydrophobic peptides. Compared to conventional “wet” intradermal (ID) administration, “dry” peptide delivered via MNs was retained for longer in the skin and whilst topical hydration of the skin with vehicle or steroid accelerated loss of ID-delivered peptide from the skin, MN delivery of peptide was unaffected. Furthermore, MN delivery resulted in enhanced presentation of antigen to T cells in skin draining lymph nodes (LNs) both 3 and 10 days after administration. Repeated administration of islet antigen peptide via MN was effective at reducing antigen-specific T cell proliferation in the pancreatic LN, although topical steroid therapy did not enhance this. Taken together, these data show auto-antigenic peptide delivery into skin using coated MNs results in prolonged retention and enhanced antigen presentation compared to conventional ID delivery and this approach may have potential in individuals identified as being at a high risk of developing type 1 diabetes and other autoimmune diseases

    The nuclear matter modification at intermediate energies. Nonnucleon targets and suppression of the resonances production at nucleus

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    A new hypothesis of hadron interactions with the nuclear matter is discussed. It is supposed that the well-known particles and resonances as well as nucleons may serve as a target in the nucleus. The experimental data on CC, dC, CTa, pC interactions at 4.2 GeV/c/nucleon were used for testing the hypothesis. A certain suppression of the DELTA(1232)P sub 3 sub 3 , N(1440)P sub 1 sub 1 isobars and rho-mesons production is observed in these interactions, compared to nucleon-nucleon interactions. It may be caused by formation of the so-called dense 'resonance matter' in the nucleus. Special experiments with multiple rising statistics are required to examine the hypothesi

    The nuclear matter modification at intermediate energies

    No full text
    A new hypothesis on hadron interactions with nuclear matter is discussed. It is supposed that the well-known particles and resonances as well as nucleons might serve as a target in the nucleus. The experimental data on CC, dC, CTa, pC interactions at 4.2 GeV/c/nucleon are used for the testing of the hypothesis. A certain suppression of production of the DELTA(1232) P sub 3 sub 3 , (1440) P sub 1 sub 1 isobars and rho mesons is observed in these interactions, compared to the nucleon-nucleon interactions. It may be caused by the formation of the so-called dense 'resonance matter' in the nucleus. Special experiments with multiple rising statistics are required to examine the hypothesi
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