Medicines for Malaria Venture, Geneva, Switzerland.
Chiba-Nishi General Hospital, Chiba, Japan.
PLoS Negl Trop Dis. 2020 Jan 30;14(1):e0007860. doi: 10.1371/journal.pntd.0007860. eCollection 2020 Jan.
In the past two decades there has been a significant expansion in the number of new therapeutic monoclonal antibodies (mAbs) that are approved by regulators. The discovery of these new medicines has been driven primarily by new approaches in inflammatory diseases and oncology, especially in immuno-oncology. Other recent successes have included new antibodies for use in viral diseases, including HIV. The perception of very high costs associated with mAbs has led to the assumption that they play no role in prophylaxis for diseases of poverty. However, improvements in antibody-expression yields and manufacturing processes indicate this is a cost-effective option for providing protection from many types of infection that should be revisited. Recent technology developments also indicate that several months of protection could be achieved with a single dose. Moreover, new methods in B cell sorting now enable the systematic identification of high-quality antibodies from humanized mice, or patients. This Review discusses the potential for passive immunization against schistosomiasis, fungal infections, dengue, and other neglected diseases.
在过去的二十年中,监管机构批准的新型治疗性单克隆抗体(mAb)数量显著增加。这些新药的发现主要是由炎症性疾病和肿瘤学领域的新方法驱动的,尤其是免疫肿瘤学。其他最近的成功案例包括用于病毒疾病的新型抗体,包括 HIV。人们认为 mAb 成本非常高,因此认为它们在预防贫困疾病方面没有作用。然而,抗体表达产量和制造工艺的改进表明,这是一种从许多类型的感染中提供保护的具有成本效益的选择,应该重新考虑。最近的技术发展还表明,单次给药即可实现数月的保护。此外,B 细胞分选的新方法现在可以从人源化小鼠或患者中系统地鉴定高质量的抗体。这篇综述讨论了针对血吸虫病、真菌感染、登革热和其他被忽视疾病的被动免疫的潜力。