Phougat Neetu, Khatri Savita, Singh Anu, Dangi Mrridula, Kumar Manish, Dabur Rajesh, Chhillar Anil Kumar
Centre for Biotechnology, Maharshi Dayanand University, Rohtak, Haryana-124001, India.
Comb Chem High Throughput Screen. 2014 Jan;17(1):53-67. doi: 10.2174/13862073113166660065.
Therapeutic options for many infections are extremely limited and at crisis point. We run the risk of entering a second pre-antibiotic era. There had been no miracle drug for the patients infected by resistant microbial pathogens. Most of the very few new drugs under development have problems with their toxicity, or pharmacokinetics and pharmacodynamics. We are already decades behind in the discovery, characterization and development of new antimicrobials. In that scenario, we could not imagine surviving without newer and effective antimicrobial agents. Bacteria have been the champions of evolution and are still evolving continuously, where they pose serious challenges for humans. Along with the crisis of evolving resistance, the condition is made worst by the meager drug pipeline for new antimicrobials. Despite ongoing efforts only 2 new antibiotics (Telavancin in 2009 and Ceftaroline fosamil in 2010) have been approved since 2009 pipeline status report of Infectious Disease Society of America (IDSA). Recent approval of new combination based antiviral drugs such as Stribild (combination of four drugs for HIV treatment) and Menhibrix (combination vaccine to prevent meningococcal disease and Haemophilus influenzae type b in children) proves that combination therapy is still the most promising approach to combat the ever evolving pathogens. Combination therapy involves the drug repurposing and regrouping of the existing antimicrobial agents to provide a synergistic approach for management of infectious diseases. This review article is an effort to highlight the challenges in new drug development and potential of combination drug therapy to deal with them.
许多感染的治疗选择极其有限,已处于危机时刻。我们面临进入第二个抗生素前时代的风险。对于感染耐药微生物病原体的患者来说,一直没有神奇的药物。目前正在研发的极少数新药大多存在毒性、药代动力学和药效学方面的问题。在新抗菌药物的发现、特性描述和研发方面,我们已经落后了几十年。在这种情况下,我们无法想象没有更新、更有效的抗菌药物该如何生存。细菌一直是进化的佼佼者,并且仍在不断进化,这给人类带来了严峻挑战。随着耐药性不断演变的危机,新抗菌药物研发渠道匮乏使情况变得更糟。自美国传染病学会(IDSA)2009年发布药物研发进展报告以来,尽管一直在努力,但仅批准了2种新抗生素(2009年的特拉万星和2010年的头孢洛林酯)。最近批准的基于新组合的抗病毒药物,如用于治疗HIV的四药组合药物Stribild和用于预防儿童脑膜炎球菌病和b型流感嗜血杆菌的联合疫苗Menhibrix,证明联合治疗仍然是对抗不断演变的病原体最有前景的方法。联合治疗涉及对现有抗菌药物进行重新利用和重新组合,以提供一种协同方法来管理传染病。这篇综述文章旨在强调新药研发中的挑战以及联合药物治疗应对这些挑战的潜力。