A Novel Therapeutic for Invasive Candidiasis
A Novel Therapeutic for Invasive Candidiasis
批准号:
8871683
负责人:
GILL DIAMOND
金额:
$75.0万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-07-01 至 2017-06-30
关键词:
Adverse effectsAntifungal AgentsAntifungal AntibioticsBiological AssayBloodCandidaCandida albicansCandidiasisClinicClinicalClinical ResearchCollaborationsDataDevelopmentDigestionDisseminated candidiasisDoseDose FractionationDrug KineticsDrug resistanceEnsureEnzymesFundingGoalsHealthHepatocyteHost DefenseHourHumanImmuneIn VitroInfectionIntramuscularKidneyKineticsLeadLiverMammalian CellMaximum Tolerated DoseMeasuresMembraneMicrobeMusMycosesNo-Observed-Adverse-Effect LevelOral candidiasisOrganPatientsPeptide HydrolasesPharmaceutical ChemistryPharmaceutical PreparationsPharmacodynamicsPharmacologic SubstancePhasePlasmaPropertyProtein BindingProteinsRattusResearch Project GrantsResistanceResistance developmentSafetySerial PassageSeriesSerumSmall Business Innovation Research GrantStructureStructure-Activity RelationshipTechnologyTestingTherapeuticTissuesToxic effectTreatment Protocolsanimal efficacyantimicrobial drugbasecommercializationcytotoxicityin vivokillingsmembrane activitymimeticsmortalitynovelnovel therapeuticsreceptorresearch studyresistance mechanismresistant strainsubcutaneous
中文摘要
描述(由申请人提供):系统性真菌感染越来越常见,特别是在免疫功能低下的患者中。虽然新的抗真菌药物已经开发出来,但与这些感染相关的死亡率仍然很高,特别是那些由白色念珠菌引起的感染,其他非白色念珠菌(NAS)。这是由于药物的范围有限,严重的副作用,以及耐药性的发展,导致耐药菌株的增加。宿主防御蛋白(hdp)是一种天然存在的广谱抗菌剂,近年来作为治疗性抗生素和抗真菌药物被研究。它们的主要优点是微生物通常不会对这些药物产生耐药性。不幸的是,它们的生产成本很高,而且往往对蛋白酶消化很敏感。我们已经证明了一系列廉价的非肽低聚物和化合物的有效活性,它们在结构和活性上模仿HDPs,在体外和体内对抗与口腔念珠菌病相关的白色念珠菌临床菌株。我们的初步数据表明,几种模拟物在人血清存在下对临床分离的白色念珠菌具有相似的抗真菌活性,其中一种化合物对播散性念珠菌病小鼠非常有效。我们相信这些化合物可以为开发对抗系统性真菌感染的新疗法奠定基础。我们的目标是确定一种安全有效的HDP模拟物作为治疗播散性念珠菌病的发展先导。
英文摘要
DESCRIPTION (provided by applicant): Systemic fungal infections are increasingly common, especially in immune compromised patients. While new antifungal drugs have been developed, there is still a high mortality associated with these infections, especially those due to Candida albicans, other non-albicans species (NAS). This is due to the limited spectrum of the drugs, significant side effects, as well as the development of resistance, leading to an increase in drug-resistant strains. Host defense proteins (HDPs) are naturally occurring, broad-spectrum antimicrobial agents that have been examined recently for their utility as therapeutic antibiotics and antifungals. Chief among their strengths is that microbes do not generally develop resistance to these agents. Unfortunately, they are expensive to produce and are often sensitive to protease digestion. We have demonstrated the potent activity of a series of inexpensive non-peptidic oligomers and compounds that mimic HDPs in both structure and activity against clinical strains of C. albicans associated with oral candidiasis, both in vitro and in vivo. Our preliminary data demonstrate similar antifungal activity for several mimetics against clinical isolates of C. albicans in the presence of human serum and one of these compounds was robustly efficacious in a mouse of disseminated candidiasis. We believe these compounds can form the basis for the development of novel therapies against systemic fungal infections. Our goal is to identify a safe and efficacious HDP mimic(s) as a development lead for treatment of disseminated candidiasis.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1038/s41598-017-04462-6
发表时间:
2017-06-28
期刊:
Scientific reports
影响因子:
4.6
作者:
[Menzel LP, Chowdhury HM, Masso-Silva JA, Ruddick W, Falkovsky K, Vorona R, Malsbary A, Cherabuddi K, Ryan LK, DiFranco KM, Brice DC, Costanzo MJ, Weaver D, Freeman KB, Scott RW, Diamond G]
通讯作者:
Diamond G
DOI:
10.3390/jof4010030
发表时间:
2018-02-27
期刊:
Journal of fungi (Basel, Switzerland)
影响因子:
--
作者:
[Chowdhury MH, Ryan LK, Cherabuddi K, Freeman KB, Weaver DG, Pelletier JC, Scott RW, Diamond G]
通讯作者:
Diamond G
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