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关于替恩依的花费，详见：“Generic HIV drugs will widen US treatment net，” Nature （August 15，2012）.
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关于HIV患者与年长者的神经生理学，详见：“Pathways to neurodegeneration：effects of HIV and aging on resting-state functional connectivity，” Neurology （2013）；“Where does HIV hide？A focus on the central nervous system，” Current opinion in HIV and AIDS （2013）.
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关于HIV对于神经的侵入状况，详见：“HIV-associated neurocognitive disorder：pathogenesis and therapeutic opportunities，” Journal of Neuroimmune Pharmacology 5（2010）.
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HIV阳性患者在发达国家的平均寿命近年来有跃升趋势，详见：“Life expectancy of individuals on combination antiretroviral therapy in high-income countries：a collaborative analysis of 14 cohort studies，” Lancet 372（2008）；“Potential gains in life expectancy from reducing heart disease，cancer，Alzheimer’s disease，kidney disease or HIV/AIDS as major causes of death in the USA，” Public Health （2013）.
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早期即开始进行抗病毒治疗的患者，其平均寿命的延长状况，详见：“Projected life expectancy of people with HIV according to timing of diagnosis，” AIDS 26（2012）.
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25 兑现承诺
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《以毒攻毒》是由考夫曼执导的一部短片，由红灯出品。详见：http：//focusforwardfilms.com/films/72/fire-with-fire.
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关于费城儿童医院所进行的CART-19临床试验的更多细节，详见他们官方网站上的内容：http：//www.chop.edu/service/oncology/pediatric-cancer-research/t-cell-therapy.html；http：//www.chop.edu/system/galleries/download/pdfs/articles/oncology/summit-grupp -cart19.pdf.
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关于艾米莉·怀特海德的更多故事，详见她的网站。在网站中，她母亲卡里·怀特海德已将其经验用编年方式列出（http：//emilywhitehead.com），并收录于：“In Girl’s Last Hope，Altered Immune Cells Beat Leukemia，” New York Times （December 9，2012）.
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关于朱恩的背景信息，援引自个人访谈内容。
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关于骨髓移植与冷战的信息，引自：“Atomic Medicine：the Cold War Origins of Origins of Biological Research，” History Today 59（2009）.
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所有关于莱文的背景信息，援引自个人访谈。
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朱恩和莱文合著了一篇文章，讲述其CCR5基因疗法的操作方法：“Blocking HIV’s attack，” Scientific American 306（2012）.
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莱文和朱恩注意到的一篇关于树突状细胞的论文：“Antiviral effect and ex vivo CD4+ T cell proliferation in HIV-positive patients as a result of CD28 co-stimulation，” Science 272（1996）.
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关于兰菲尔的背景信息，援引自个人访谈。
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关于锌指核酸酶（ZFN）的开发与应用，可进一步参见：“Zinc finger nucleases：custom-designed molecular scissors for genome engineering of plant and mammalian cells，” Nucleic Acids Research 33（2005）.
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关于SIV、HIV，可进一步参见：“Where the wild things are：pathogenesis of SIV infection in African nonhuman primate hosts” HIV\AIDS Reports 7（2010）以及“Natural SIV hosts：showing AIDS the door，” Science 335（2012）.
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关于SIV已经演化超过32000年的证据，详见：“Islander biogeography reveals the deep history of SIV，” Science 329（2010）.
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关于SIV感染，发病猴与不发病猴的模型比较，详见：“AIDS pathogenesis：a tale of two monkeys，” Journal of Medical Primatology 37（2008）.
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关于人类与黑鼠B6之间基因型的相似度，详见：“Of Mice and Men：Striking Similarities at the DNA Level Could Aid Research，” San Francisco Chronicle （December 5，2002）.
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关于小鼠和人类之间基因表现的比较，详见：“Genomic responses in mouse models poorly mimic human inflammatory diseases，” Proceedings of the National Academy of Sciences of the United States of America 110（Feb 2013）.
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人源化小鼠的HIV感染模型文献回顾，详见：“Humanized mouse models of HIV infection，” AIDS Reviews 13（3）：135-148（2011）.
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部分研究者并不相信人源化小鼠可提供任何有价值的治疗模型。该意见详见：“The mouse is out of the bag：insights and perspectives on HIV-1-infected humanized mouse models，” Experimental Biology and Medicine 236（2011）.
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朱恩在以毒攻毒的人源化小鼠上给予锌指核酸酶的试验结果，详见：“Establishment of HIV-1 resistance in CD4+ T cells by genome editing using zinc-finger nucleases，” Nature Biotechnology 26（2008）.
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朱恩在HIV阳性志愿者中进行的CCR5 ZFN临床试验的结果，发表于：“HAART treatment interruption following adoptive transfer of zinc finger nuclease（ZFN）modified autologous CD4+ T-cells（SB-728-T）to HIV-infected subjects demonstrates durable engraftment and suppression of viral load，” Abstract #165，18th Conference on Retroviruses and Opportunistic Infections，Boston，MA（2011）；“Induction of acquired CCR5 deficiency with zinc finger nuclease-modified autologous CD4 T cells（SB-728-T）correlates with increases in CD4 count and effects on viral load in HIV-infected subjects，” Abstract #155，19th Conference on Retroviruses and Opportunistic Infections，Seattle，WA（2012）.
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