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AdCD40L 基因治疗对自发性犬恶性黑色素瘤的治疗效果和免疫刺激作用。

Treatment efficacy and immune stimulation by AdCD40L gene therapy of spontaneous canine malignant melanoma.

机构信息

University Animal Hospital, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.

出版信息

J Immunother. 2013 Jul-Aug;36(6):350-8. doi: 10.1097/CJI.0b013e31829d8a1b.

Abstract

Malignant melanoma is a serious disease in both humans and dogs, and the high metastatic potential results in poor prognosis for many patients. Its similarities with human melanoma make spontaneous canine melanoma an excellent model for comparative studies of novel therapies and tumor biology. We report a pilot study of local adenovector CD40L (AdCD40L) immunogene treatment in 19 cases of canine melanoma (14 oral, 4 cutaneous, and 1 conjunctival). Three patients were World Health Organization stage I, 2 were stage II, 10 stage III, and 4 stage IV. One to 6 intratumoral injections of AdCD40L were given every 7 days, followed by cytoreductive surgery in 9 cases and only immunotherapy in 10 cases. Tumor tissue was infiltrated with T and B lymphocytes after treatment, suggesting immune stimulation. The best overall response included 5 complete responses, 8 partial responses, and 4 stable and 2 progressive disease statuses according to the World Health Organization response criteria. Median survival was 160 days (range, 20-1141 d), with 3 dogs still alive at submission. Our results suggest that local AdCD40L therapy is safe and could have beneficial effects in dogs, supporting further treatment development. Clinical translation to human patients is in progress.

摘要

恶性黑色素瘤是人类和犬类的一种严重疾病,其高转移性导致许多患者预后不良。犬自发性黑色素瘤与人类黑色素瘤具有相似性,使其成为新型治疗方法和肿瘤生物学比较研究的理想模型。我们报告了一项初步研究,即局部腺病毒 CD40L(AdCD40L)免疫基因治疗 19 例犬黑色素瘤(14 例口腔、4 例皮肤和 1 例结膜)的情况。其中 3 例为世界卫生组织(WHO)I 期,2 例为 II 期,10 例为 III 期,4 例为 IV 期。每 7 天进行 1 至 6 次瘤内注射 AdCD40L,然后在 9 例病例中进行细胞减灭性手术,在 10 例病例中仅进行免疫治疗。治疗后肿瘤组织中浸润了 T 和 B 淋巴细胞,表明免疫刺激。根据 WHO 反应标准,最佳总反应包括 5 例完全缓解、8 例部分缓解和 4 例稳定和 2 例进展疾病状态。中位生存时间为 160 天(范围 20-1141 天),提交时仍有 3 只狗存活。我们的结果表明,局部 AdCD40L 治疗是安全的,并且可能对犬类产生有益效果,支持进一步的治疗开发。临床转化为人类患者正在进行中。

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