Rust Lauren N, Ricciardi Michael J, Lutz Savannah S, Yusova Sofiya, Louw Johan J, Yrizarry-Medina Aaron, Biswas Sreya, Fischer Miranda, Barber-Axthelm Aaron, Zilverberg Gavin, Bailey Lauren, Swanson Tonya, Tonelli Rachael, McElfresh G W, Rosen Brandon C, Voigt Thomas B, Panayiotou Christakis, Mauter Jack T, Ghosh Noor, Meanor Jenna, Godoy Giovana, Axthelm Michael, Smedley Jeremy, Slifka Mark K, Kallas Esper G, Webb Gabriela, Zweig Robert, Labriola Caralyn S, Bimber Benjamin N, Sacha Jonah B, Watkins David I, Burwitz Benjamin J
Oregon National Primate Research Center (ONPRC), Oregon Health and Science University, Beaverton, Oregon, USA.
Mabloc LLC, Washington DC, USA.
JCI Insight. 2025 Jul 15;10(16). doi: 10.1172/jci.insight.191665. eCollection 2025 Aug 22.
Yellow fever virus (YFV) infection is fatal in 5%-10% of the 200,000 yearly cases. There is currently no available antiviral treatment. We showed previously that administration of 50 mg/kg of a YFV-specific neutralizing monoclonal antibody (nmAb) at 2 days postinfection (dpi), prior to the onset of severe disease, protected YFV-infected rhesus macaques from death. To further explore the clinical applicability of our nmAb MBL-YFV-01, we treated rhesus macaques with a lower dose (10 mg/kg) of this nmAb prophylactically or therapeutically at 3.5 dpi. We show that a single prophylactic or therapeutic i.v. dose of our nmAb protects rhesus macaques from death following challenge. A comprehensive analysis of 167 inflammatory cytokine and chemokines revealed that protection was associated with significantly reduced expression of 125 of these markers, including type I IFN, IL-6, and CCL2. This study further expands the potential clinical use of our YFV-specific nmAb, which could be used during an outbreak for immediate prophylactic immunity or for patients with measurable serum viremia.
黄热病病毒(YFV)感染在每年20万例病例中有5%-10%是致命的。目前尚无可用的抗病毒治疗方法。我们之前表明,在感染后2天(dpi)、严重疾病发作之前给予50mg/kg的YFV特异性中和单克隆抗体(nmAb),可保护感染YFV的恒河猴免于死亡。为了进一步探索我们的nmAb MBL-YFV-01的临床适用性,我们在3.5 dpi时用较低剂量(10mg/kg)的这种nmAb对恒河猴进行预防性或治疗性治疗。我们发现,单次静脉注射预防性或治疗性剂量的nmAb可保护恒河猴在受到攻击后免于死亡。对167种炎性细胞因子和趋化因子的综合分析表明,保护作用与这些标志物中125种的表达显著降低有关,包括I型干扰素、IL-6和CCL2。这项研究进一步扩大了我们的YFV特异性nmAb的潜在临床应用范围,该nmAb可在疫情爆发期间用于立即获得预防性免疫或用于有可测量血清病毒血症的患者。