Global health perspectives on antibacterial drug discovery and the preclinical pipeline

被引:0
|
作者
Theuretzbacher, Ursula [1 ]
Jumde, Ravindra P. [2 ]
Hennessy, Alan [2 ]
Cohn, Jennifer [2 ]
Piddock, Laura J. V. [2 ]
机构
[1] Ctr Antiinfect Agents, Vienna, Austria
[2] Global Antibiot Res & Dev Partnership, Geneva, Switzerland
关键词
ANTIMICROBIAL RESISTANCE; STAPHYLOCOCCUS-AUREUS; ANTIBIOTIC-RESISTANCE; INHIBITORS; CHALLENGES; BINDING; MECHANISMS; ANTIBODIES; INNOVATION; BACTERIA;
D O I
10.1038/s41579-025-01167-w
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Antibacterial resistance is a global challenge that requires a coordinated international response. The current clinical pipeline largely consists of derivatives of established antibiotic classes, whereas the discovery and preclinical pipeline is diverse and innovative including new direct-acting agents with no cross-resistance with existing antibiotics. These novel compounds target pathways such as lipoprotein synthesis, lipopolysaccharide biosynthesis and transport, outer membrane assembly, peptidoglycan biosynthesis, fatty acid biosynthesis and isoprenoid biosynthesis. If these agents can be developed into safe, effective and affordable drugs, they could address a broad range of infections worldwide, benefiting large patient populations without geographical limitations. However, strategies such as indirect-acting or pathogen-specific treatments are likely to benefit small patient groups, primarily in high-income countries that have advanced health-care systems and diagnostic infrastructure. Although encouraging, the discovery and preclinical pipeline remains insufficiently robust to offset the high attrition rates typical of early-stage drug innovation and to meet global health needs.
引用
收藏
页数:17
相关论文
共 50 条
  • [31] Preclinical models for drug discovery for metastatic disease
    Wakefield, Lalage
    Agarwal, Seema
    Tanner, Kandice
    CELL, 2023, 186 (08) : 1792 - 1813
  • [32] Mitigating risk in academic preclinical drug discovery
    Dahlin, Jayme L.
    Inglese, James
    Walters, Michael A.
    NATURE REVIEWS DRUG DISCOVERY, 2015, 14 (04) : 279 - 294
  • [33] Mitigating risk in academic preclinical drug discovery
    Jayme L. Dahlin
    James Inglese
    Michael A. Walters
    Nature Reviews Drug Discovery, 2015, 14 : 279 - 294
  • [34] Preclinical drug discovery research and training at Vanderbilt
    Lindsley, Craig W.
    Weaver, David
    Jones, Carrie
    Marnett, Larry
    Conn, P. Jeffrey
    ACS CHEMICAL BIOLOGY, 2007, 2 (01) : 17 - 20
  • [35] Hot topic: Preclinical Profiling in Drug Discovery
    Wienkers, Larry C.
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2010, 13 (02) : 88 - 89
  • [36] The importance of preclinical models for cholangiocarcinoma drug discovery
    Krendl, Felix J.
    Primavesi, Florian
    Oberhuber, Rupert
    Neureiter, Daniel
    Ocker, Matthias
    Bekric, Dino
    Kiesslich, Tobias
    Mayr, Christian
    EXPERT OPINION ON DRUG DISCOVERY, 2025, 20 (02) : 205 - 216
  • [37] Enhancing preclinical drug discovery with artificial intelligence
    Vijayan, R. S. K.
    Kihlberg, Jan
    Cross, Jason B.
    Poongavanam, Vasanthanathan
    DRUG DISCOVERY TODAY, 2022, 27 (04) : 967 - 984
  • [38] Tackling reproducibility in academic preclinical drug discovery
    Frye, Stephen V.
    Arkin, Michelle R.
    Arrowsmith, Cheryl H.
    Conn, P. Jeffrey
    Glicksman, Marcie A.
    Hull-Ryde, Emily A.
    Slusher, Barbara S.
    NATURE REVIEWS DRUG DISCOVERY, 2015, 14 (11) : 733 - 734
  • [39] The Role of Permeation Assays in Preclinical Drug Discovery
    Mertlikova-Kaiserova, Helena
    CHEMICKE LISTY, 2023, 117 (12): : 739 - 746
  • [40] Tackling reproducibility in academic preclinical drug discovery
    Stephen V. Frye
    Michelle R. Arkin
    Cheryl H. Arrowsmith
    P. Jeffrey Conn
    Marcie A. Glicksman
    Emily A. Hull-Ryde
    Barbara S. Slusher
    Nature Reviews Drug Discovery, 2015, 14 : 733 - 734