HIV preferentially infects HIV-specific CD4+ T cells

HIV infection is associated with the progressive loss of CD4(+) T cells through their destruction or decreased production. A central, yet unresolved issue of HIV disease is the mechanism for this loss, and in particular whether HIV-specific CD4(+) T cells are preferentially affected. Here we show that HIV-specific memory CD4(+) T cells in infected individuals contain more HIV viral DNA than other memory CD4(+) T cells, at all stages of HIV disease. Additionally, following viral rebound during interruption of antiretroviral therapy, the frequency of HIV viral DNA in the HIV-specific pool of memory CD4(+) T cells increases to a greater extent than in memory CD4(+) T cells of other specificities. These findings show that HIV-specific CD4(+) T cells are preferentially infected by HIV in vivo. This provides a potential mechanism to explain the loss of HIV-specific CD4(+) T-cell responses, and consequently the loss of immunological control of HIV replication. Furthermore, the phenomenon of HIV specifically infecting the very cells that respond to it adds a cautionary note to the practice of structured therapy interruption.     

Systemic Research Practices Towards the Development of an Eco-Community in Vietnam: some Joint Post-Facto Reflections

In this article we discuss how an interdisciplinary research team partnered with a variety of stakeholders concerned with and/or affected by the impacts of climate change in the Red River Delta of Vietnam. The research, undertaken from 2016 to 2018, drew upon a wide range of methods to investigate systemically these impacts – with a view to the research inputting into the development of (more) sustainable ways of living. The research solicited various accounts of the experience of climate change in the community, set up learning processes in community meetings, and created an interface with government officials positioned at commune, district, provincial, and national levels. The intention was to offer support towards developing a learning process (broadly defined as including learnings/systemic inquiry across organizational levels of the society) to pursue options for sustainable living. The article offers our post-facto reflections which render more explicit (to ourselves and for the benefit of audiences) how the research team, with Hoang as lead researcher, facilitated the inquiry process towards developing a synthesis which underscored the assets for resilience to climate change and supported interventions to strengthen such (defined) assets.

     

本溪地区BIF中玄武质围岩的高场强元素特征

辽宁本溪地区条带状铁矿(BIF)与其玄武质火山围岩之间的时空关联非常密切.对于玄武质火山围岩高场强元素(HFSE)的研究表明:wNb/wTa比值(7.00~19.93)表现出明显的分异,而wZr/wHf比值(33.46~38.28)则变化不大;从弓长岭到南芬、歪头山样品的wNb/wTa比值变化具有明显的循序性.这种高场强元素的迁移和分异特征反映出俯冲作用与盆地演化之间的关联.研究区玄武质火山围岩(wNb/wYb)N比值大于1(1.21~18.45,平均2.72),这进一步表明,其形成的构造背景为陆内弧后盆地提供了有利于BIF形成的条件.     

基于热压块的不锈钢粉尘还原实验

为了从不锈钢粉尘中回收利用Fe,Cr和Ni等,对不锈钢粉尘热压块制备及其自还原过程进行了研究.在热压温度为200℃,热压压力为35 MPa条件下,抗压强度达到900 N/个以上.高温条件下,煤热解产生的挥发分可参与不锈钢粉尘还原反应,当还原温度为1 400,1 450℃时,挥发分还原作用率达到0.4.据XRD分析和热力学计算,自还原过程中含铬物质的物相转变顺序为Fe Cr2O4,Cr2O3,Cr7C3,[Cr]Fe-Cr-Ni-C.当还原温度为1 450℃,烟煤中固定碳与粉尘中可去除氧的物质量的比(xc/xo)为0.72时,不锈钢粉尘热压块不能完全还原;当xc/xo大于0.8,还原20 min时,不锈钢粉尘热压块能完全还原.     

Accelerated vaccination for Ebola virus haemorrhagic fever in non-human primates

Containment of highly lethal Ebola virus outbreaks poses a serious public health challenge. Although an experimental vaccine has successfully protected non-human primates against disease, more than six months was required to complete the immunizations, making it impractical to limit an acute epidemic. Here, we report the development of accelerated vaccination against Ebola virus in non-human primates. The antibody response to immunization with an adenoviral (ADV) vector encoding the Ebola glycoprotein (GP) was induced more rapidly than with DNA priming and ADV boosting, but it was of lower magnitude. To determine whether this earlier immune response could nonetheless protect against disease, cynomolgus macaques were challenged with Ebola virus after vaccination with ADV-GP and nucleoprotein (NP) vectors. Protection was highly effective and correlated with the generation of Ebola-specific CD8(+) T-cell and antibody responses. Even when animals were immunized once with ADV-GP/NP and challenged 28 days later, they remained resistant to challenge with either low or high doses of virus. This accelerated vaccine provides an intervention that may help to limit the epidemic spread of Ebola, and is applicable to other viruses.