Department of Companion Animals and Horses, Division of Equine Surgery, Research Group Oncology, University of Veterinary Medicine, Vienna, Austria.
BlueSky Immunotherapies, Vienna, Austria.
PLoS One. 2021 Nov 19;16(11):e0260155. doi: 10.1371/journal.pone.0260155. eCollection 2021.
Bovine papillomaviruses types 1 and 2 (BPV1, BPV2) commonly induce skin tumours termed sarcoids in horses and other equids. Sarcoids seriously compromise the health and welfare of affected individuals due to their propensity to resist treatment and reoccur in a more severe form. We have developed influenza (Flu) A and B virus vectors that harbour a truncated NS1 gene (iNS) assuring interferon induction and co-express shuffled BPV1 E6 and E7 antigens for sarcoid immunotherapy. In a safety trial involving 12 healthy horses, intradermal administration of iNSA/E6E7equ and iNSB/E6E7equ was well tolerated, with the only transient side effect being mild fever in four horses. Repeated screening of secretions and faeces by RT-PCR and plaque assay revealed no virus shedding, thus also confirming biological safety. In a patient trial involving 29 horses bearing BPV1-induced single or multiple sarcoids, at least one lesion per horse was intratumourally injected and then boosted with iNSA/E6E7equ and/or iNSB/E6E7equ. The treatment induced a systemic antitumour response as reflected by the synchronous regression of injected and non-injected lesions. Irrespective of vaccination schemes, complete tumour regression was achieved in 10/29 horses. In 10/29 horses, regression is still ongoing (May 2021). Intriguingly, scrapings collected from former tumour sites in two patients tested negative by BPV1 PCR. Nine severely affected individuals with a history of unsuccessful therapeutic attempts did not (6/29) or only transiently (3/29) respond to the treatment. INSA/E6E7equ and iNSB/E6E7equ proved safe and effective in significantly reducing the tumour burden even in severe cases.
牛乳头瘤病毒 1 型和 2 型(BPV1、BPV2)通常会导致马和其他马科动物的皮肤肿瘤,称为肉瘤。由于肉瘤具有抵抗治疗和以更严重形式复发的倾向,因此严重影响了受影响个体的健康和福利。我们开发了携带截断 NS1 基因(iNS)的流感(Flu)A 和 B 病毒载体,以确保干扰素诱导,并共同表达 shuffl 的 BPV1 E6 和 E7 抗原用于肉瘤免疫治疗。在一项涉及 12 匹健康马的安全性试验中,iNSA/E6E7equ 和 iNSB/E6E7equ 的皮内给药耐受性良好,唯一的短暂副作用是四匹马轻度发热。通过 RT-PCR 和噬斑分析对分泌物和粪便进行重复筛查,未发现病毒脱落,从而也确认了生物安全性。在一项涉及 29 匹患有 BPV1 诱导的单发或多发肉瘤的患者试验中,每匹马的至少一个病变部位被肿瘤内注射,然后用 iNSA/E6E7equ 和/或 iNSB/E6E7equ 进行加强。治疗诱导了全身性抗肿瘤反应,反映在注射和未注射病变的同步消退。无论接种方案如何,29 匹马中有 10 匹马完全消退。在 29 匹马中,仍在继续消退(2021 年 5 月)。有趣的是,两名患者的来自先前肿瘤部位的刮取物经 BPV1 PCR 检测呈阴性。9 名曾接受过不成功治疗尝试的严重受影响个体未(29/6)或仅短暂(29/3)对治疗产生反应。INSA/E6E7equ 和 iNSB/E6E7equ 被证明是安全有效的,即使在严重情况下,也能显著降低肿瘤负担。