25 research outputs found

    From \u27Wonderful Americans\u27 to the AHCA: Contrasting Trump\u27s Nomination Acceptance Address and his Administration\u27s Actions on GLBTQ Health

    Get PDF
    Donald Trump\u27s 2016 Nomination Acceptance Address at the Republican National Convention explicitly mentioned GLBTQ people as Trump promised to “protect our LGBTQ citizens” and called GLBTQ people “wonderful Americans.” However, since Trump\u27s inauguration, he has appointed anti-GLBTQ leaders, proposed cuts to HIV research, and offered his support for a ban on transgender recruits to the military. This article begins with a close reading of Trump\u27s speech, showing how Trump expresses ostensible support for GLBTQ Americans, only to capitalize on the deaths of queer and trans people of color at the Pulse Nightclub in Orlando mere weeks before the convention by pitting GLBTQ people against “Islamic terrorism.” The second half of the article then examines the effects of Trump\u27s appointments and policy priorities on GLBTQ people and their families. The contrast between Trump\u27s speech and his presidency reveals that Trump values the deaths, but not the lives, of GLBTQ people

    31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016) : part two

    Get PDF
    Background The immunological escape of tumors represents one of the main ob- stacles to the treatment of malignancies. The blockade of PD-1 or CTLA-4 receptors represented a milestone in the history of immunotherapy. However, immune checkpoint inhibitors seem to be effective in specific cohorts of patients. It has been proposed that their efficacy relies on the presence of an immunological response. Thus, we hypothesized that disruption of the PD-L1/PD-1 axis would synergize with our oncolytic vaccine platform PeptiCRAd. Methods We used murine B16OVA in vivo tumor models and flow cytometry analysis to investigate the immunological background. Results First, we found that high-burden B16OVA tumors were refractory to combination immunotherapy. However, with a more aggressive schedule, tumors with a lower burden were more susceptible to the combination of PeptiCRAd and PD-L1 blockade. The therapy signifi- cantly increased the median survival of mice (Fig. 7). Interestingly, the reduced growth of contralaterally injected B16F10 cells sug- gested the presence of a long lasting immunological memory also against non-targeted antigens. Concerning the functional state of tumor infiltrating lymphocytes (TILs), we found that all the immune therapies would enhance the percentage of activated (PD-1pos TIM- 3neg) T lymphocytes and reduce the amount of exhausted (PD-1pos TIM-3pos) cells compared to placebo. As expected, we found that PeptiCRAd monotherapy could increase the number of antigen spe- cific CD8+ T cells compared to other treatments. However, only the combination with PD-L1 blockade could significantly increase the ra- tio between activated and exhausted pentamer positive cells (p= 0.0058), suggesting that by disrupting the PD-1/PD-L1 axis we could decrease the amount of dysfunctional antigen specific T cells. We ob- served that the anatomical location deeply influenced the state of CD4+ and CD8+ T lymphocytes. In fact, TIM-3 expression was in- creased by 2 fold on TILs compared to splenic and lymphoid T cells. In the CD8+ compartment, the expression of PD-1 on the surface seemed to be restricted to the tumor micro-environment, while CD4 + T cells had a high expression of PD-1 also in lymphoid organs. Interestingly, we found that the levels of PD-1 were significantly higher on CD8+ T cells than on CD4+ T cells into the tumor micro- environment (p < 0.0001). Conclusions In conclusion, we demonstrated that the efficacy of immune check- point inhibitors might be strongly enhanced by their combination with cancer vaccines. PeptiCRAd was able to increase the number of antigen-specific T cells and PD-L1 blockade prevented their exhaus- tion, resulting in long-lasting immunological memory and increased median survival

    Return to Teamsterville: A reconsideration and dialogue on ethnography and critique

    No full text
    As the places of monuments are reconsidered today in light of social justice concerns, the authors revisit a “monument” of language and social interaction (LSI) research. Philipsen’s foundational work published nearly 50 years ago, “Speaking ‘Like a Man’ in Teamsterville,” thus becomes a starting point for dialogue among four scholars with diverse views on the critical voice in ethnography of communication research. When read today, the homophobic speech of Teamstervillers is shocking. Also surprising by present standards is that such speech passes unremarked and does not figure in the analysis. In the present essay, the authors—an LSI scholar, discourse studies scholar, critical rhetorical scholar, and an LSI doctoral student—review early debates on the critical voice, relate individual narratives of their experiences in either reading “Teamsterville” again after a long hiatus or encountering the work for the first time, and then conduct a joint dialogue on the question: What is the ethnographer’s obligation when harmful and oppressive speech is observed? Though their views remain diverse, the authors advocate for a disciplinary consensus: that the present moment calls for renewed discussion—and, even if differently practiced, affirmation—of the critical voice in the ethnography of communication
    corecore