scholarly journals The epidemiological consequences of immune priming

2012 ◽  
Vol 279 (1746) ◽  
pp. 4505-4512 ◽  
Author(s):  
Hannah J. Tidbury ◽  
Alex Best ◽  
Mike Boots
Keyword(s):  
Immune Response ◽  
Population Dynamics ◽  
Population Level ◽  
Low Doses ◽  
Population Stability ◽  
Invertebrate Immunity ◽  
Invertebrate Host ◽  
Immune Priming ◽  
Pathogen Persistence ◽  
Full Immunity

Exposure to low doses of pathogens that do not result in the host becoming infectious may ‘prime’ the immune response and increase protection to subsequent challenge. There is increasing evidence that such immune priming is a widespread and important feature of invertebrate host–pathogen interactions. Immune priming clearly has implications for individual hosts but will also have population-level implications. We present a susceptible–primed–infectious model—in contrast to the classic susceptible–infectious–recovered framework—to investigate the impacts of immune priming on pathogen persistence and population stability. We describe impacts of immune priming on the epidemiology of the disease in both constant and seasonal environments. A key result is that immune priming may act to destabilize population dynamics. In particular, when the proportion of individuals becoming primed rather than infected is high, but this priming does not confer full immunity, the population may be strongly destabilized through the generation of limit cycles. We discuss the implications of our model both in the context of invertebrate immunity and more widely.

scholarly journals Chemotactic Responses of Jurkat Cells in Microfluidic Flow-Free Gradient Chambers

Micromachines ◽  
2020 ◽  
Vol 11 (4) ◽  
pp. 384 ◽  
Author(s):  
Utku M. Sonmez ◽  
Adam Wood ◽  
Kyle Justus ◽  
Weijian Jiang ◽  
Fatima Syed-Picard ◽  
...  
Keyword(s):  
Immune Response ◽  
Cancer Progression ◽  
Soft Lithography ◽  
Cell Movement ◽  
Population Level ◽  
Jurkat Cells ◽  
Dependent Manner ◽  
Diverse Range ◽  
Microfluidic Flow ◽  
Cell Motion

Gradients of soluble molecules coordinate cellular communication in a diverse range of multicellular systems. Chemokine-driven chemotaxis is a key orchestrator of cell movement during organ development, immune response and cancer progression. Chemotaxis assays capable of examining cell responses to different chemokines in the context of various extracellular matrices will be crucial to characterize directed cell motion in conditions which mimic whole tissue conditions. Here, a microfluidic device which can generate different chemokine patterns in flow-free gradient chambers while controlling surface extracellular matrix (ECM) to study chemotaxis either at the population level or at the single cell level with high resolution imaging is presented. The device is produced by combining additive manufacturing (AM) and soft lithography. Generation of concentration gradients in the device were simulated and experimentally validated. Then, stable gradients were applied to modulate chemotaxis and chemokinetic response of Jurkat cells as a model for T lymphocyte motility. Live imaging of the gradient chambers allowed to track and quantify Jurkat cell migration patterns. Using this system, it has been found that the strength of the chemotactic response of Jurkat cells to CXCL12 gradient was reduced by increasing surface fibronectin in a dose-dependent manner. The chemotaxis of the Jurkat cells was also found to be governed not only by the CXCL12 gradient but also by the average CXCL12 concentration. Distinct migratory behaviors in response to chemokine gradients in different contexts may be physiologically relevant for shaping the host immune response and may serve to optimize the targeting and accumulation of immune cells to the inflammation site. Our approach demonstrates the feasibility of using a flow-free gradient chamber for evaluating cross-regulation of cell motility by multiple factors in different biologic processes.

scholarly journals Immune Control of Herpesvirus Infection in Molluscs

Pathogens ◽  
2020 ◽  
Vol 9 (8) ◽  
pp. 618
Author(s):  
Jacinta R Agius ◽  
Serge Corbeil ◽  
Karla J Helbig
Keyword(s):  
Immune Response ◽  
Adaptive Immune System ◽  
Herpesvirus Infection ◽  
Viable Option ◽  
Important Species ◽  
Immune Priming ◽  
Adaptive Immune ◽  
Preventative Strategy ◽  
Herpesvirus 1 ◽  
Ostreid Herpesvirus 1

Molluscan herpesviruses that are capable of infecting economically important species of abalone and oysters have caused significant losses in production due to the high mortality rate of infected animals. Current methods in preventing and controlling herpesviruses in the aquacultural industry are based around biosecurity measures which are impractical and do not contain the virus as farms source their water from oceans. Due to the lack of an adaptive immune system in molluscs, vaccine related therapies are not a viable option; therefore, a novel preventative strategy known as immune priming was recently explored. Immune priming has been shown to provide direct protection in oysters from Ostreid herpesvirus-1, as well as to their progeny through trans-generational immune priming. The mechanisms of these processes are not completely understood, however advancements in the characterisation of the oyster immune response has assisted in formulating potential hypotheses. Limited literature has explored the immune response of abalone infected with Haliotid herpesvirus as well as the potential for immune priming in these species, therefore, more research is required in this area to determine whether this is a practical solution for control of molluscan herpesviruses in an aquaculture setting.

scholarly journals Proteolytic Remodeling of Perineuronal Nets: Effects on Synaptic Plasticity and Neuronal Population Dynamics

2018 ◽  
Vol 2018 ◽  
pp. 1-13 ◽  
Author(s):  
P. Lorenzo Bozzelli ◽  
Seham Alaiyed ◽  
Eunyoung Kim ◽  
Sonia Villapol ◽  
Katherine Conant
Keyword(s):  
Population Dynamics ◽  
Synaptic Plasticity ◽  
Synaptic Input ◽  
Neuronal Plasticity ◽  
Population Level ◽  
Gamma Oscillations ◽  
Brain Regions ◽  
Neuronal Population ◽  
Perineuronal Nets ◽  
Perineuronal Net

The perineuronal net (PNN) represents a lattice-like structure that is prominently expressed along the soma and proximal dendrites of parvalbumin- (PV-) positive interneurons in varied brain regions including the cortex and hippocampus. It is thus apposed to sites at which PV neurons receive synaptic input. Emerging evidence suggests that changes in PNN integrity may affect glutamatergic input to PV interneurons, a population that is critical for the expression of synchronous neuronal population discharges that occur with gamma oscillations and sharp-wave ripples. The present review is focused on the composition of PNNs, posttranslation modulation of PNN components by sulfation and proteolysis, PNN alterations in disease, and potential effects of PNN remodeling on neuronal plasticity at the single-cell and population level.

TLR2-mediated innate immune priming boosts lung anti-viral immunity

2020 ◽  
pp. 2001584
Author(s):  
Jason Girkin ◽  
Su-Ling Loo ◽  
Camille Esneau ◽  
Steven Maltby ◽  
Francesca Mercuri ◽  
...  
Keyword(s):  
Gene Expression ◽  
Immune Response ◽  
Innate Immunity ◽  
Viral Load ◽  
Epithelial Cell ◽  
Epithelial Cells ◽  
Immune Cell ◽  
Innate Immune ◽  
Immune Priming ◽  
Tlr2 Activation

Research questionAssessment of whether TLR2 activation boosts the innate immune response to rhinovirus infection, as a treatment strategy for virus-induced respiratory diseases.MethodsWe employed treatment with a novel TLR2 agonist (INNA-X) prior to rhinovirus infection in mice, and INNA-X treatment in differentiated human bronchial epithelial cells derived from asthmatic-donors. We assessed viral load, immune cell recruitment, cytokines, type I and III IFN production, as well as the lung tissue and epithelial cell immune transcriptome.ResultsWe show in vivo, that a single INNA-X treatment induced innate immune priming characterised by low-level IFN-λ, Fas ligand, chemokine expression and airway lymphocyte recruitment. Treatment 7-days before infection significantly reduced lung viral load, increased IFN-β/λ expression and inhibited neutrophilic inflammation. Corticosteroid treatment enhanced the anti-inflammatory effects of INNA-X. Treatment 1-day before infection increased expression of 190 lung tissue immune genes. This tissue gene expression signature was absent with INNA-X treatment 7-days before infection, suggesting an alternate mechanism, potentially via establishment of immune cell-mediated mucosal innate immunity. In vitro, INNA-X treatment induced a priming response defined by upregulated IFN-λ, chemokine and anti-microbial gene expression that preceded an accelerated response to infection enriched for NF-κB-regulated genes and reduced viral loads, even in epithelial cells derived from asthmatic donors with intrinsic delayed anti-viral immune response.ConclusionAirway epithelial cell TLR2 activation induces prolonged innate immune priming, defined by early NF-κB activation, IFN-λ expression and lymphocyte recruitment. This response enhanced anti-viral innate immunity and reduced virus-induced airway inflammation.

scholarly journals Neonatal treatment with low doses of anti-idiotypic antibody leads to the expression of a silent clone.

1981 ◽  
Vol 153 (4) ◽  
pp. 1004-1008 ◽  
Author(s):  
J Hiernaux ◽  
C Bona ◽  
P J Baker
Keyword(s):  
Immune Response ◽  
Low Doses ◽  
Newborn Mice ◽  
Myeloma Protein ◽  
Neonatal Treatment ◽  
Beta 2 ◽  
Idiotypic Antibody

BALB/c mice immunized with bacterial levan (BL) produce an immune response that fails to generate antibody expressing the idiotype (Id) of the beta (2 leads to 6) fructosan-binding myeloma protein ABPC 48 (A48). Pretreatment of newborn BALB/c mice (at 1 d of age) with 0.01-10 microgram of affinity purified BALB/c anti-A48 Id antibody followed by immunization with BL 1-2 mo later produces an anti-BL response that expresses the A48 Id. This shows that A48 Id+ anti-BL clones belong to a normally silent fraction of the anti-BL repertoire. The activation of A48 Id+ anti-BL clones anti-A48 Id antibody is specific because the pretreatment of newborn mice with anti-MOPC 384 Id antibody, followed by immunization with BL, does not lead to its activation. Moreover, pretreatment of mice with anti-A48 Id antibody does not alter the MOPC 460 Id+ component of the anti-TNP response. It is also important to note that the activation of the A48 Id+ clone in pretreated mice requires subsequent immunization with BL.

scholarly journals The consequences of polyandry for population viability, extinction risk and conservation

2013 ◽  
Vol 368 (1613) ◽  
pp. 20120053 ◽  
Author(s):  
Luke Holman ◽  
Hanna Kokko
Keyword(s):  
Population Dynamics ◽  
Extinction Risk ◽  
Population Level ◽  
Female Fitness ◽  
Male Care ◽  
Negative Effect ◽  
Adverse Environmental Conditions ◽  
The Cost ◽  
Cost Of Sex ◽  
Population Fitness

Polyandry, by elevating sexual conflict and selecting for reduced male care relative to monandry, may exacerbate the cost of sex and thereby seriously impact population fitness. On the other hand, polyandry has a number of possible population-level benefits over monandry, such as increased sexual selection leading to faster adaptation and a reduced mutation load. Here, we review existing information on how female fitness evolves under polyandry and how this influences population dynamics. In balance, it is far from clear whether polyandry has a net positive or negative effect on female fitness, but we also stress that its effects on individuals may not have visible demographic consequences. In populations that produce many more offspring than can possibly survive and breed, offspring gained or lost as a result of polyandry may not affect population size. Such ecological ‘masking’ of changes in population fitness could hide a response that only manifests under adverse environmental conditions (e.g. anthropogenic change). Surprisingly few studies have attempted to link mating system variation to population dynamics, and in general we urge researchers to consider the ecological consequences of evolutionary processes.

scholarly journals From global to local scale: where is the best for conservation purpose?

2020 ◽  
Vol 30 (1) ◽  
pp. 183-200
Author(s):  
Elena Sulis ◽  
Gianluigi Bacchetta ◽  
Donatella Cogoni ◽  
Giuseppe Fenu
Keyword(s):  
Population Dynamics ◽  
Local Level ◽  
Demographic Data ◽  
Conservation Status ◽  
Population Level ◽  
Local Scale ◽  
Local Analysis ◽  
Vital Rates ◽  
Spanish Populations ◽  
Local Trend

AbstractDemographic analysis of plant populations represents an essential conservation tool allowing to identify the population trends both at global and at the local level. In this study, the population dynamics of Helianthemum caput-felis (Cistaceae) was investigated at the local level by monitoring six populations distributed in Sardinia, Balearic Islands and Ibero-Levantine coast (Alicante). Demographic data for each population were analysed by performing Integral Projection Models (IPMs). Our results showed that, although the local trend of the main basic demographic functions was similar, vital rates and demographic dynamics varied among populations indicating high variability. In fact, asymptotic growth rate in Spanish populations widely varied both between years and populations (some populations growth, decline or strongly decline), while Sardinian populations showed greater equilibrium or a slight increase. Also, the typical pattern of a long-lived species was not supported by the results at the local scale. These results indicated that different populations of the same species can present extremely different population dynamics and support the belief that, for conservation needs, local studies are more informative than global ones: the conservation status of H. caput-felis could notably vary at a small spatial scale and, accordingly, the conservation efforts must be planned at the population level and supported by local analysis.

Modulation of embryonic development due to mating with immunised males

2017 ◽  
Vol 29 (3) ◽  
pp. 565 ◽  
Author(s):  
Ludmila A. Gerlinskaya ◽  
Svetlana O. Maslennikova ◽  
Margaret V. Anisimova ◽  
Nataly A. Feofanova ◽  
Evgenii L. Zavjalov ◽  
...  
Keyword(s):  
Population Level ◽  
Paternal Effects ◽  
Adaptation Mechanism ◽  
Immune Priming ◽  
Gm Csf ◽  
In Utero Environment ◽  
Macrophage Colony Stimulating Factor ◽  
Macrophage Colony ◽  
Stimulation Of

The modification of pre- and postnatal development conferred by immunogenic stimulation of mothers provides a population-level adaptation mechanism for non-genetic transfer of maternal experiences to progeny. However little is known about the transmission of paternal immune experiences to offspring. Here, we show that immune priming of males 3–9 days before mating affects the growth and humoral environment of developing embryos of outbred (ICR) and inbred (C57BL and BALB/c) mice. Antigenic stimulation of fathers caused a significant increase in embryonic bodyweight as measured on Day 16 of pregnancy and altered other gestation parameters, such as feto–placental ratio. Pregnant females mated with immunised males were also characterised by changes in humoral conditions as shown by measurements of blood and amniotic progesterone, testosterone and granulocyte–macrophage colony-stimulating factor (GM-CSF) cytokine concentrations. These results emphasise the role of paternal effects of immune priming on the in utero environment and fetal growth.

Expression and Immune Response to Islet Antigens following Treatment with Low Doses of Streptozotocin in H-2dMice

1997 ◽  
Vol 10 (1) ◽  
pp. 17-25 ◽  
Author(s):  
Kevan C. Herold ◽  
Elizabeth Baumann ◽  
Vaiva Vezys ◽  
Frank Buckingham
Keyword(s):  
Immune Response ◽  
Low Doses
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