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    <title>DSpace Collection:</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9073</link>
    <description />
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      <rdf:Seq>
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/9214" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/9213" />
        <rdf:li rdf:resource="http://localhost:8080/xmlui/handle/123456789/9211" />
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    </items>
    <dc:date>2026-04-09T00:49:20Z</dc:date>
  </channel>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/9214">
    <title>Interplay of host and viral factors in inflammatory pathway mediated cytokine storm during RNA virus infection</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9214</link>
    <description>Title: Interplay of host and viral factors in inflammatory pathway mediated cytokine storm during RNA virus infection
Authors: Chaudhary, Riya; Meher, Aparna; Krishnamoorthy, Pandikannan; Kumar, Himanshu
Abstract: RNA viruses always have been a serious concern for human health by causing several outbreaks, often pandemics.&#xD;
The excessive mortality and deaths associated with the outbreaks caused by these viruses were due to the&#xD;
excessive induction of pro-inflammatory cytokines leading to cytokine storm. Cytokines are important for cell-tocell&#xD;
communication to maintain cell homeostasis. Disturbances of this homeostasis can lead to intricate chain&#xD;
reactions resulting in a massive release of cytokines. This could lead to a severe self-reinforcement of several&#xD;
feedback processes, which could eventually cause systemic harm, multiple organ failure, or death. Multiple&#xD;
inflammation-associated pathways were involved in the cytokine production and its regulation. Different RNA&#xD;
viruses induce these pathways through the interplay with their viral factors and host proteins and miRNAs&#xD;
regulating these pathways. This review will discuss the interplay of host proteins and miRNAs that can play an&#xD;
important role in the regulation of cytokine storm and the possible therapeutic potential of these molecules for&#xD;
the treatment and the challenges associated with the clinical translation</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/9213">
    <title>Nanoparticles cellular uptake, trafficking, activation, toxicity and in vitro evaluation</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9213</link>
    <description>Title: Nanoparticles cellular uptake, trafficking, activation, toxicity and in vitro evaluation
Authors: Toscano, Fernanda; Torres-Arias, Marbel
Abstract: Nanoparticles (NPs) physicochemical properties, such as size, shape, surface chemistry, charge, etc., play a critical role in biological systems interactions, which&#xD;
include NPs’ cellular uptake, trafficking, activation, and toxicity. Although nano-bio interactions are multifaceted and complex, their assessment is essential for&#xD;
future therapeutic and diagnostic use since being carriers that deliver specific molecules (i.e., active pharmaceutical ingredients and imaging agents) in intracellular&#xD;
sites. The journey of NPs begins by reaching the plasma membrane and entering the cell mainly through endocytosis. After vesicles pinch off the cell membrane, the&#xD;
intracellular trafficking is mediated by a network of cellular endosomes which direct NPs to the different cellular components. Otherwise, NPs or their contents are&#xD;
released into the cytoplasm. In both cases, NPs can pass undetected or be recognized by the cell leading to a pro or anti-inflammatory response. Indeed, the cell&#xD;
response mostly depends on cell type and NPs physicochemical properties. The principal mechanism by which NPs activate the cell response is RONS production.&#xD;
Other mechanism includes signaling pathways modulation related to metabolic and enzymatic reactions, cell transduction, and immune modulation. Hence, the&#xD;
underlying mechanisms of cellular and subcellular interactions in vitro should be performed to provide insights into NPs’ effect. This information helps us to improve&#xD;
their synthesis and design to maximize the clinical benefits while minimizing side effects. Most in vitro tests to evaluate NPs’ effect in cells were developed focusing on&#xD;
cell dysfunctions, cytotoxicity, genotoxicity, immunogenicity, and cell death.</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/9211">
    <title>The efficacy, safety, and immunogenicity of plague vaccines: A systematic literature review</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9211</link>
    <description>Title: The efficacy, safety, and immunogenicity of plague vaccines: A systematic literature review
Authors: Hartley, Louise; Harold, Sydney; Hawe, Emma
Abstract: Plague remains endemic in many parts of the world, and despite efforts, no preventative vaccine is available. We&#xD;
performed a systemic review of available randomised controlled trials (RCTs) of live, attenuated, or killed plague&#xD;
vaccines vs. placebo, no intervention, or other plague vaccine to evaluate their efficacy, safety, and immunogenicity.&#xD;
Data sources included MEDLINE, Embase, and the Cochrane Library; clinical trial registers; and&#xD;
reference lists of included studies. Primary outcomes were efficacy, safety, and immunogenicity. Risk of bias was&#xD;
assessed using the Cochrane Collaborations tool. Only 2 RCTs, both on subunit vaccines, were included out of the&#xD;
75 screened articles. The 2 trials included 240 participants with a follow-up of 3 months and 60 participants with&#xD;
a follow-up of 13 months, respectively. Safety evidence was limited, but both vaccines were well tolerated, with&#xD;
only mild to moderate adverse events. Both vaccines were immunogenic in a dose-dependent manner. However,&#xD;
given the limited data identified in this systematic review, we are unable to quantify the efficacy of vaccines to&#xD;
prevent plague, as well as their long-term safety and immunogenicity. More trials of plague vaccines are needed&#xD;
to generate additional evidence of their long-term effects.</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://localhost:8080/xmlui/handle/123456789/9210">
    <title>Functional role of the TGF-β signaling in the Drosophila immune response</title>
    <link>http://localhost:8080/xmlui/handle/123456789/9210</link>
    <description>Title: Functional role of the TGF-β signaling in the Drosophila immune response
Authors: Bastin, Ashley; Eleftherianos, Ioannis
Abstract: TGF-β signaling pathways are present in diverse animal species, which indicates their evolutionary importance in&#xD;
modulating several conserved biological processes and maintaining host homeostasis by adjusting the activity of&#xD;
innate immune mechanisms. Drosophila melanogaster utilizes two related but separable cascades of the canonical&#xD;
TGF-β signaling pathway: The Bone Morphogenetic Protein and Activin branches. Recent studies have produced&#xD;
significant information on the immune role of TGF-β signaling in the fruit fly model during response against&#xD;
certain bacterial pathogens. Results from further investigations have generated novel insights into the role of&#xD;
Drosophila TGF-β signaling molecules as immune regulators opposing infection against nematode parasites and&#xD;
their mutualistic bacterial partners. This knowledge has revealed a previously unknown layer of the host innate&#xD;
immune system. Here we summarize these recent breakthroughs focusing on the participation of TGF-β signaling&#xD;
factors in various Drosophila immune processes in relation to infection with potent bacteria and nematode&#xD;
parasites. The presented information provides important clues indicating directions for future research into the&#xD;
design of novel strategies for the effective control of infectious diseases caused by bacterial pathogens and&#xD;
parasitic nematodes.</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
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