Saunders Kevin O, Pegu Amarendra, Georgiev Ivelin S, Zeng Ming, Joyce M Gordon, Yang Zhi-Yong, Ko Sung-Youl, Chen Xuejun, Schmidt Stephen D, Haase Ashley T, Todd John-Paul, Bao Saran, Kwong Peter D, Rao Srinivas S, Mascola John R, Nabel Gary J
Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Department of Microbiology, University of Minnesota, Minneapolis, Minnesota, USA.
J Virol. 2015 Jun;89(11):5895-903. doi: 10.1128/JVI.00210-15. Epub 2015 Mar 18.
Pathogen-specific neutralizing antibodies protect against many viral infections and can potentially prevent human immunodeficiency virus (HIV) transmission in humans. However, neutralizing antibodies have so far only been shown to protect nonhuman primates (NHP) against lentiviral infection when given shortly before challenge. Thus, the clinical utility and feasibility of passive antibody transfer to confer long-term protection against HIV-1 are still debated. Here, we investigate the potential of a broadly neutralizing HIV-1 antibody to provide long-term protection in a NHP model of HIV-1 infection. A human antibody was simianized to avoid immune rejection and used to sustain therapeutic levels for ∼5 months. Two months after the final antibody administration, animals were completely protected against viral challenge. These findings demonstrate the feasibility and potential of long-term passive antibody for protection against HIV-1 in humans and provide a model to test antibody therapies for other diseases in NHP.
Antibodies against HIV are potential drugs that may be able to prevent HIV infection in humans. However, the long-term protective capacity of antibodies against HIV has not been assessed. Here, we repetitively administered a macaque version of a human anti-HIV antibody to monkeys, after which the antibody persisted in the blood for >5 months. Moreover, the antibody could be sustained at protective levels for 108 days, conferring protection 52 days after the last dose in a monkey model of HIV infection. Thus, passive antibody transfer can provide durable protection against infection by viruses that cause AIDS in primates.
病原体特异性中和抗体可预防多种病毒感染,并有可能预防人类免疫缺陷病毒(HIV)在人类中的传播。然而,到目前为止,中和抗体仅在攻击前不久给予时才显示能保护非人灵长类动物(NHP)免受慢病毒感染。因此,被动抗体转移以提供针对HIV-1的长期保护的临床实用性和可行性仍存在争议。在此,我们研究一种广泛中和HIV-1的抗体在HIV-1感染的NHP模型中提供长期保护的潜力。一种人源抗体被猿猴化以避免免疫排斥,并用于维持约5个月的治疗水平。在最后一次抗体给药后两个月,动物完全受到保护免受病毒攻击。这些发现证明了长期被动抗体在人类中预防HIV-1的可行性和潜力,并提供了一个在NHP中测试针对其他疾病的抗体疗法的模型。
抗HIV抗体是可能能够预防人类HIV感染的潜在药物。然而,抗HIV抗体的长期保护能力尚未得到评估。在此,我们向猴子重复给药人源抗HIV抗体的猕猴版本,之后该抗体在血液中持续存在超过5个月。此外,该抗体可在保护水平维持108天,在HIV感染的猴子模型中最后一剂后52天提供保护。因此,被动抗体转移可提供针对灵长类动物中导致艾滋病的病毒感染的持久保护。