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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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2011年，米利曼医学指数评估了朱恩团队在自体移植上，给予CCR5锌指核酸的花费，为363800美元。因此这也使得自体移植的花费，较终身抗病毒疗程的花费节省了将近30万美元。详见：http：//publications. milliman.com/research/health-rr/pdfs/2011-us-organ-tissue. pdf.
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26 有个孩子被治愈了，那又如何
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一名染上HIV的儿童被治愈的报道，详见：“Functional HIV cure after very early ART of an infected infant，” Abstract #48LB，20th Conference on Retroviruses and Opportunistic Infections，Atlanta，GA（2013）.
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关于布卢和瓦格纳的谈话内容，详见：“Revolutionary treatment begins，” University of Minnestota News （April 24，2013）.
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布朗打给布卢的电话内容，详见：“Babies could be key to HIV cure，” Washington Blade （Aplril 26，2013）.
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关于马戈利斯的背景信息，引述自个人访谈。
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关于组蛋白去乙酰酶抑制剂（HDACi）在癌症治疗上的历史，与伏立诺他作为第一种由FDA核准的药剂等，详见：“Histone deacetylase（HDAC）inhibitors in recent clinical trials for cancer therapy，” Clinical Epigenetics 1（Dec 2010）.
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马戈利斯对HDACi的一种——丙戊酸进行的调查，详见：“Coaxing HIV-1 from resting CD4 T cells：histone deacetylase inhibition allows latent viral expression，” AIDS 18（May 21，2004），and “Depletion of latent HIV-1 infection in vivo：a proof-of-concept study，” Lancet 366（Aug 13，2005）.
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马戈利斯测试伏立诺他的数据，详见：“Expression of latent HIV induced by the potent HDAC inhibitor suberoylanilide hydroxamic acid，” AIDS Research and Human Retroviruses 25（Feb 2009）.
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马戈利斯撰写了一篇关于HDACi的精彩文献回顾，详见：“Histone deacetylase inhibitors HIV latency，” Current Opinion in HIV and AIDS 6（2011）.
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马戈利斯为大众所做的演讲内容，详见：“Administration of vorinostat disrupts HIV-1 latency in patients on ART，” Abstract #157LB，19th Conference on Retroviruses and Opportunistic Infections，Seattle，WA（2012）.
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莱温将其对伏立诺他的试验数据与分析结果，分享于：“HIV latency and eradication：clinical perspectives，” Abstract #106，19th Conference on Retroviruses and Opportunistic Infections，Seattle，WA（2012）.
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“这是有史以来，我们首度证明有方法可以专门针对潜伏病毒，这是迈向治愈HIV感染的第一步。”此话引述自莱温，收录于：“Drug helps purge hidden HIV virus，UNC study shows” from the University of North Carolina School of Medicine（March 8，2012）.
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27 锌指一弹
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以我学位论文的研究结果为基础，坎农与我合著了一篇论文：“Zinc finger nuclease-mediated CCR5 knockout hematopoietic stem cell transplantation controls HIV-1 in vivo，” Nature Biotechnology 28（Aug 2010）.
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坎农的背景信息，援引自个人访谈。
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加州再生医学研究所为“梦之队”提供了资助，此事详见：http：//www.cirm.ca.gov/our-funding/awards/ziinc-finger-nuclease-based-stem-cell-therapy-aids.
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坎农所说的“这方法能奏效，就像是‘根本理所当然嘛’！这是最稀松平常的事情。我那时还没心理准备，看到其他人对这些结果叹为观止”。摘录自：“Locking Out HIV，” CIRM Annual Report （2011）.
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关于亨里奇与库里茨克斯的背景信息，援引自个人访谈。
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亨里奇第一篇关于波士顿病人的结果，详见：“Long-term reduction in peripheral blood HIV-1 reservoirs following reduced-intensity conditioning allogeneic stem cell transplantation in two HIV-positive individuals，” Abstract THAA0101，XIX International AIDS Conference，Washington，DC（2012）.
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