380 research outputs found

    Women, Westernization and the Origins of Modern Vietnamese Theatre

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    Modern spoken theatre emerged in Vietnam in the context of intellectual and social upheaval in the 1920s and 1930s. Plays in this period focused on the status of women, the effects of Westernization and the emergence of Vietnamese nationalism. In Nam Xuong\u27s 1930 play, Ong Tay An-nam, women became conduits through which men expressed their Westernized or nationalist identities

    Women in the Frontlines of Revolution in Myanmar

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    Women in Myanmar have played a vital role in the pro-democracy movement since the 2021 coup. They have taken on combat roles and have been involved in non-lethal resistance efforts, such as mobilizing and organizing the local population and fundraising. However, despite their critical roles and contributions, they lack proportionate representation in leadership positions within the pro-democracy National Unity Government (NUG), National Unity Consultative Council (NUCC), and People Defense Forces (PDF). This has resulted in non-lethal efforts receiving very few resources and provisions. Additionally, the lack of representation in leadership positions has led to discrimination and sexual assault for women soldiers on the frontlines. It is crucial for the NUG and resistance coalition forces to harness the power of these women influencers and leaders by using a coherent Strategic Communication strategy and providing the resources and support they need to continue their efforts. Furthermore, it is important for the NUG, NUCC, and PDFs to address the issue of discrimination and sexual assault against women soldiers and ensure that women have equal representation in leadership positions. The participation and leadership of women in the pro-democracy movement can greatly contribute to the resiliency of the people and the sustained rejection of the military junta.https://digital-commons.usnwc.edu/wps/1029/thumbnail.jp

    Call for Papers, Issue 5/2024

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    IL-22 mediates goblet cell hyperplasia and worm expulsion in intestinal helminth infection.

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    Type 2 immune responses are essential in protection against intestinal helminth infections. In this study we show that IL-22, a cytokine important in defence against bacterial infections in the intestinal tract, is also a critical mediator of anti-helminth immunity. After infection with Nippostrongylus brasiliensis, a rodent hookworm, IL-22-deficient mice showed impaired worm expulsion despite normal levels of type 2 cytokine production. The impaired worm expulsion correlated with reduced goblet cell hyperplasia and reduced expression of goblet cell markers. We further confirmed our findings in a second nematode model, the murine whipworm Trichuris muris. T.muris infected IL-22-deficient mice had a similar phenotype to that seen in N.brasiliensis infection, with impaired worm expulsion and reduced goblet cell hyperplasia. Ex vivo and in vitro analysis demonstrated that IL-22 is able to directly induce the expression of several goblet cell markers, including mucins. Taken together, our findings reveal that IL-22 plays an important role in goblet cell activation, and thus, a key role in anti-helminth immunity

    Cationic Amino Acid Transporter-2 Regulates Immunity by Modulating Arginase Activity

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    Cationic amino acid transporters (CAT) are important regulators of NOS2 and ARG1 activity because they regulate L-arginine availability. However, their role in the development of Th1/Th2 effector functions following infection has not been investigated. Here we dissect the function of CAT2 by studying two infectious disease models characterized by the development of polarized Th1 or Th2-type responses. We show that CAT2βˆ’/βˆ’ mice are significantly more susceptible to the Th1-inducing pathogen Toxoplasma gondii. Although T. gondii infected CAT2βˆ’/βˆ’ mice developed stronger IFN-Ξ³ responses, nitric oxide (NO) production was significantly impaired, which contributed to their enhanced susceptibility. In contrast, CAT2βˆ’/βˆ’ mice infected with the Th2-inducing pathogen Schistosoma mansoni displayed no change in susceptibility to infection, although they succumbed to schistosomiasis at an accelerated rate. Granuloma formation and fibrosis, pathological features regulated by Th2 cytokines, were also exacerbated even though their Th2 response was reduced. Finally, while IL-13 blockade was highly efficacious in wild-type mice, the development of fibrosis in CAT2βˆ’/βˆ’ mice was largely IL-13-independent. Instead, the exacerbated pathology was associated with increased arginase activity in fibroblasts and alternatively activated macrophages, both in vitro and in vivo. Thus, by controlling NOS2 and arginase activity, CAT2 functions as a potent regulator of immunity

    IL-10R Blockade during Chronic Schistosomiasis Mansoni Results in the Loss of B Cells from the Liver and the Development of Severe Pulmonary Disease

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    In schistosomiasis patients, parasite eggs trapped in hepatic sinusoids become foci for CD4+ T cell-orchestrated granulomatous cellular infiltrates. Since the immune response is unable to clear the infection, the liver is subjected to ongoing cycles of focal inflammation and healing that lead to vascular obstruction and tissue fibrosis. This is mitigated by regulatory mechanisms that develop over time and which minimize the inflammatory response to newly deposited eggs. Exploring changes in the hepatic inflammatory infiltrate over time in infected mice, we found an accumulation of schistosome egg antigen-specific IgG1-secreting plasma cells during chronic infection. This population was significantly diminished by blockade of the receptor for IL-10, a cytokine implicated in plasma cell development. Strikingly, IL-10R blockade precipitated the development of portal hypertension and the accumulation of parasite eggs in the lungs and heart. This did not reflect more aggressive Th2 cell responsiveness, increased hepatic fibrosis, or the emergence of Th1 or Th17 responses. Rather, a role for antibody in the prevention of severe disease was suggested by the finding that pulmonary involvement was also apparent in mice unable to secrete class switched antibody. A major effect of anti-IL-10R treatment was the loss of a myeloid population that stained positively for surface IgG1, and which exhibited characteristics of regulatory/anti-inflammatory macrophages. This finding suggests that antibody may promote protective effects within the liver through local interactions with macrophages. In summary, our data describe a role for IL-10-dependent B cell responses in the regulation of tissue damage during a chronic helminth infection
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