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Intratumoral injection of the seasonal flu shot converts immunologically cold tumors to hot and serves as an immunotherapy for cancer.
瘤内注射季节性流感疫苗可将免疫冷肿瘤转化为热肿瘤,并作为癌症的免疫治疗。
- 影响因子:8.58
- DOI:10.1073/pnas.1904022116
- 作者列表:"Newman JH","Chesson CB","Herzog NL","Bommareddy PK","Aspromonte SM","Pepe R","Estupinian R","Aboelatta MM","Buddhadev S","Tarabichi S","Lee M","Li S","Medina DJ","Giurini EF","Gupta KH","Guevara-Aleman G","Rossi M","Nowicki C","Abed A","Goldufsky JW","Broucek JR","Redondo RE","Rotter D","Jhawar SR","Wang SJ","Kohlhapp FJ","Kaufman HL","Thomas PG","Gupta V","Kuzel TM","Reiser J","Paras J","Kane MP","Singer EA","Malhotra J","Denzin LK","Sant'Angelo DB","Rabson AB","Lee LY","Lasfar A","Langenfeld J","Schenkel JM","Fidler MJ","Ruiz ES","Marzo AL","Rudra JS","Silk AW","Zloza A
- 发表时间:2020-01-14
Abstract
:Reprogramming the tumor microenvironment to increase immune-mediated responses is currently of intense interest. Patients with immune-infiltrated "hot" tumors demonstrate higher treatment response rates and improved survival. However, only the minority of tumors are hot, and a limited proportion of patients benefit from immunotherapies. Innovative approaches that make tumors hot can have immediate impact particularly if they repurpose drugs with additional cancer-unrelated benefits. The seasonal influenza vaccine is recommended for all persons over 6 mo without prohibitive contraindications, including most cancer patients. Here, we report that unadjuvanted seasonal influenza vaccination via intratumoral, but not intramuscular, injection converts "cold" tumors to hot, generates systemic CD8+ T cell-mediated antitumor immunity, and sensitizes resistant tumors to checkpoint blockade. Importantly, intratumoral vaccination also provides protection against subsequent active influenza virus lung infection. Surprisingly, a squalene-based adjuvanted vaccine maintains intratumoral regulatory B cells and fails to improve antitumor responses, even while protecting against active influenza virus lung infection. Adjuvant removal, B cell depletion, or IL-10 blockade recovers its antitumor effectiveness. Our findings propose that antipathogen vaccines may be utilized for both infection prevention and repurposing as a cancer immunotherapy.
摘要
: 重新编程肿瘤微环境以增加免疫介导的反应是目前非常感兴趣的。免疫浸润 “热” 肿瘤患者表现出更高的治疗反应率和改善的生存率。然而,只有少数肿瘤是热门的,有限比例的患者受益于免疫治疗。使肿瘤发热的创新方法可以产生立竿见影的影响,特别是如果它们重新利用具有额外癌症无关益处的药物。季节性流感疫苗推荐给所有 6 个月以上没有禁忌症的人,包括大多数癌症患者。在这里,我们repor t t ha t unadjuvan t ed季节性流感疫苗t离子via在t ra t瘤,bu t no t在t瘤,injec t ion conver t s "cold" t umors t o ho t,genies t es sys t emic CD8 + T cell-media t ed an t i t umor immuni t y,和森西t化轻瘫t a t t umors t o checkpoin t封锁。重要的是,瘤内接种也提供了保护,防止随后的活动性流感病毒肺部感染。令人惊讶的是,一种基于角鲨烯的佐剂疫苗维持瘤内调节性b细胞,即使在防止活动性流感病毒肺部感染的同时,也不能改善抗肿瘤反应。佐剂去除,b细胞耗竭,或IL-10 阻断恢复其抗肿瘤效力。我们的研究结果提出,抗病原体疫苗可用于感染预防和癌症免疫治疗的再利用。
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METHODS::Blue rubber bleb naevus syndrome (BRBNS) is an extremely rare venous malformation that often manifests as multiple haemangioma-like lesions in the skin and gastrointestinal tract. The drug sirolimus plays a key role in the signalling pathway of angiogenesis and subsequent development of BRBNS and its use has been described in several case reports. We present a case series of four patients with BRBNS who exhibited good treatment response to sirolimus. All four patients were administered oral sirolimus at doses of 1.0-1.5 mg/m2 /day with a target drug level of 5-10 ng/mL and median treatment duration of 20 months. All patients had a reduction in the size of the lesions and a normalization of coagulopathy with tolerable drug adverse reactions at follow-up. Sirolimus may be effective and safe in paediatric patients with BRBNS. Further prospective studies are suggested to evaluate the long-term effectiveness of this drug.
METHODS:BACKGROUND:Human papillomavirus (HPV) infections are associated with common dermatologic and nondermatologic diseases. Although HPV vaccines are well established as preventive measures for genital warts and cervical neoplasia, their use as therapeutic agents deserves greater attention. OBJECTIVE:To evaluate the use of HPV vaccine(s) as a treatment modality for cutaneous and/or mucosal disease. METHODS:A primary literature search using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines was conducted in January 2019 by using the PubMed and Cochrane databases. RESULTS:A total of 63 articles with 4439 patients were included. The majority of patients with cutaneous warts, recurrent respiratory papillomatosis, and squamous and basal cell carcinomas were successfully treated with HPV vaccination. Preliminary data on patients with pre-existing anogenital warts, cervical intraepithelial neoplasia, anal intraepithelial neoplasia, and vulvar intraepithelial neoplasia is promising. LIMITATIONS:This review was limited by the lack of controls, patients' previous HPV vaccination status, and publication bias. CONCLUSION:The commercially available three-dose, quadrivalent HPV vaccine is a potential therapeutic option for the treatment of cutaneous warts, recurrent respiratory papillomatosis, and squamous and basal cell carcinomas. Noncommercially available HPV vaccines demonstrate therapeutic response for treating anogenital warts, cervical intraepithelial neoplasia, anal intraepithelial neoplasia, and vulvar intraepithelial neoplasia. The vaccine's efficacy as an adjunct therapy for HPV-associated cutaneous and/or mucosal disease warrants further exploration.
METHODS::Our understanding of melanoma precursors and progression to melanoma has developed as a result of advances in the field of molecular diagnostics. We now better understand the potential for genetic heterogeneity within a single lesion. Combined tumors can pose a diagnostic challenge when deciding the line between benign and malignant, which in turn has direct implications for patient management. Primary cilia (PC) are ubiquitous sensory organelles that have essential functions in cellular proliferation, differentiation, and development. The ciliation index (percentage of ciliated melanocytes) has been shown to reliably differentiate melanoma, which fail to ciliate, from melanocytic nevi, which retain PC. We therefore analyzed the potential for using the ciliation index to differentiate benign and malignant components in combined melanocytic lesions. We collected patient samples (n = 10) of unequivocal combined lesions with both melanoma and associated nevus components. Melanocytes were highlighted with SOX10 and costained with gamma-Tubulin and acetylated alpha-Tubulin to highlight the basal body and cilium, respectively. The number of melanocytes retaining cilia under high-power microscopy was examined. The melanoma component had average of 4% ciliation (SD: 7%), whereas the associated nevus component was significantly higher with 59% ciliation (SD: 17%). These data show that PC may be a reliable means of distinguishing benign from malignant components within a single tumor. The ciliation index may be a helpful tool in distinguishing challenging cases of combined lesions of melanoma in situ with a dermal nevus component from invasive melanoma, thus promoting improved staging and clinical management.
皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。