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本文引用的文献

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The case for pathogen-specific therapy.病原体特异性疗法的情况。
Expert Opin Pharmacother. 2009 Aug;10(11):1699-703. doi: 10.1517/14656560903066837.
2
Progress on the development of therapeutics against West Nile virus.抗西尼罗河病毒疗法的研发进展
Antiviral Res. 2009 Sep;83(3):214-27. doi: 10.1016/j.antiviral.2009.05.006. Epub 2009 Jun 6.
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Human monoclonal antibodies in single chain fragment variable format with potent neutralization activity against influenza virus H5N1.具有针对H5N1流感病毒的高效中和活性的单链可变片段形式的人源单克隆抗体。
Antiviral Res. 2009 Sep;83(3):238-44. doi: 10.1016/j.antiviral.2009.05.005. Epub 2009 May 27.
4
Combination therapy using chimeric monoclonal antibodies protects mice from lethal H5N1 infection and prevents formation of escape mutants.使用嵌合单克隆抗体的联合疗法可保护小鼠免受致命的H5N1感染,并防止逃逸突变体的形成。
PLoS One. 2009 May 22;4(5):e5672. doi: 10.1371/journal.pone.0005672.
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Cross-subtype neutralization sensitivity despite monoclonal antibody resistance among early subtype A, C, and D envelope variants of human immunodeficiency virus type 1.1型人类免疫缺陷病毒早期A、C和D亚型包膜变体中尽管存在单克隆抗体耐药性但仍具有交叉亚型中和敏感性
J Virol. 2009 Aug;83(15):7783-8. doi: 10.1128/JVI.00673-09. Epub 2009 May 27.
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Therapeutic antibodies: successes, limitations and hopes for the future.治疗性抗体:成功、局限与未来展望
Br J Pharmacol. 2009 May;157(2):220-33. doi: 10.1111/j.1476-5381.2009.00190.x.
7
Broadly neutralizing anti-HIV-1 antibodies disrupt a hinge-related function of gp41 at the membrane interface.广泛中和抗HIV-1抗体在膜界面破坏gp41的铰链相关功能。
Proc Natl Acad Sci U S A. 2009 Jun 2;106(22):9057-62. doi: 10.1073/pnas.0901474106. Epub 2009 May 19.
8
Utilization of immunoglobulin G Fc receptors by human immunodeficiency virus type 1: a specific role for antibodies against the membrane-proximal external region of gp41.1型人类免疫缺陷病毒对免疫球蛋白G Fc受体的利用:针对gp41膜近端外部区域抗体的特定作用。
J Virol. 2009 Aug;83(15):7397-410. doi: 10.1128/JVI.00656-09. Epub 2009 May 20.
9
Treatment of Clostridium difficile-associated disease.艰难梭菌相关性疾病的治疗
Gastroenterology. 2009 May;136(6):1899-912. doi: 10.1053/j.gastro.2008.12.070. Epub 2009 May 7.
10
Broadly neutralizing human anti-HIV antibody 2G12 is effective in protection against mucosal SHIV challenge even at low serum neutralizing titers.广泛中和性人类抗HIV抗体2G12即使在血清中和效价较低时,也能有效保护机体免受黏膜猴-人免疫缺陷病毒攻击。
PLoS Pathog. 2009 May;5(5):e1000433. doi: 10.1371/journal.ppat.1000433. Epub 2009 May 15.

基于单克隆抗体的微生物疾病治疗方法。

Monoclonal antibody-based therapies for microbial diseases.

机构信息

Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Vaccine. 2009 Dec 30;27 Suppl 6:G38-46. doi: 10.1016/j.vaccine.2009.09.105.

DOI:10.1016/j.vaccine.2009.09.105
PMID:20006139
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2810317/
Abstract

The monoclonal antibody (mAb) revolution that currently provides many new options for the treatment of neoplastic and inflammatory diseases has largely bypassed the field of infectious diseases. Only one mAb is licensed for use against an infectious disease, although there are many in various stages of development. This situation is peculiar given that serum therapy was one of the first effective treatments for microbial diseases and that specific antibodies have numerous antimicrobial properties. The underdevelopment and underutilization of mAb therapies for microbial diseases has various complex explanations that include the current availability of antimicrobial drugs, small markets, high costs and microbial antigenic variation. However, there are signs that the climate for mAb therapeutics in infectious diseases is changing given increasing antibiotic drug resistance, the emergence of new pathogenic microbes for which no therapy is available, and development of mAb cocktail formulations. Currently, the major hurdle for the widespread introduction of mAb therapies for microbial diseases is economic, given the high costs of immunoglobulin preparations and relatively small markets. Despite these obstacles there are numerous opportunities for mAb development against microbial diseases and the development of radioimmunotherapy provides new options for enhancing the magic bullet. Hence, there is cautious optimism that the years ahead will see more mAbs in clinical use against microbial diseases.

摘要

单克隆抗体(mAb)的革命为治疗肿瘤和炎症性疾病提供了许多新的选择,但在传染病领域却基本没有涉及。尽管有许多 mAb 处于不同的开发阶段,但只有一种获得了用于传染病治疗的许可。鉴于血清疗法是治疗微生物疾病的首批有效疗法之一,并且特定抗体具有许多抗菌特性,这种情况很特殊。造成针对微生物疾病的 mAb 疗法发展和利用不足的原因有很多,包括目前抗菌药物的可用性、市场规模较小、成本高以及微生物抗原变异等。然而,鉴于抗生素药物耐药性不断增加、出现了尚无治疗方法的新致病性微生物,以及 mAb 鸡尾酒制剂的开发,mAb 在传染病治疗方面的应用前景正在发生变化。目前,鉴于免疫球蛋白制剂成本高,市场相对较小,针对微生物疾病广泛引入 mAb 疗法的主要障碍是经济方面的。尽管存在这些障碍,但针对微生物疾病开发 mAb 仍有许多机会,放射性免疫疗法为增强“神奇子弹”提供了新的选择。因此,人们谨慎乐观地认为,未来几年将有更多的 mAb 用于治疗微生物疾病。