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两种不同剂量的白细胞介素-15 超激动剂复合物(ALT-803)在原位膀胱癌小鼠模型中的疗效。

Effectiveness of two different dose administration regimens of an IL-15 superagonist complex (ALT-803) in an orthotopic bladder cancer mouse model.

机构信息

Translational and Clinical Research Program, University of Hawaii Cancer Center, 701 Ilalo Street Suite 353, Honolulu, HI, 96813, USA.

Department of Molecular Biosciences and Bioengineering, University of Hawaii at Manoa, Honolulu, HI, USA.

出版信息

J Transl Med. 2019 Jan 17;17(1):29. doi: 10.1186/s12967-019-1778-6.

Abstract

BACKGROUND

We set out to determine if the administration of subcutaneous (SQ) ALT-803 was non-inferior to standard intravesical BCG treatment in a carcinogen induced mouse (C57BL/6J) bladder cancer model.

METHODS

Using this well-established carcinogen induced mouse model, we studied the effects of various dosing schemas of ALT-803 (SQ alone, SQ with intravesical BCG, intravesical alone, intravesical with intravesical BCG) compared to intravesical BCG alone (positive control) and PBS (negative control). The non-inferiority margin for the difference in bladder weight, as a surrogate for tumor mass, was defined as 7%.

RESULTS

All treatment groups (i.e., ALT-803 SQ alone, ALT-803 SQ with intravesical BCG, ALT-803 intravesical alone, ALT-803 intravesical with intravesical BCG and intravesical BCG alone) demonstrated a significant reduction in tumor burden as evident by bladder weights and H&E stain (p < 0.005). Non-inferiority tests between the intravesical BCG alone group and the additional treatment groups showed that SQ ALT-803 alone (p = 0.04) and BCG plus SQ ALT-803 (p = 0.009) were non-inferior to intravesical BCG alone. In this model, we did not see an appreciable infiltration of CD4 T, CD8 T or CD161/KLRB1 natural killer (NK) cells in the bladder/tumor. When assessing peripheral blood mononuclear cells, SQ ALT-803 alone resulted in a robust induction of CD8 T cells (p < 0.01), NKG2D NK cells (p < 0.005) and CD3/NKG2D NKT cells (p < 0.005) compared to other groups, while in splenic tissue, SQ ALT-803 alone resulted in a robust induction of CD3/NKG2D NKT cells (p < 0.005) compared to other groups.

CONCLUSION

Subcutaneous ALT-803 treatment alone or in combination with intravesical BCG was well tolerated and was not inferior to intravesical BCG alone. CD8 T, NKG2D NK and CD3/NKG2D NKT cell induction along with induction of key cytokines remain steadfast mechanisms behind ALT-803. The enhanced therapeutic index seen with BCG and ALT-803, administered SQ or intravesically, provides a powerful justification for the further development of these regimens.

摘要

背景

我们旨在确定在致癌物诱导的小鼠(C57BL/6J)膀胱癌模型中,皮下(SQ)ALT-803 给药是否不劣于标准膀胱内卡介苗(BCG)治疗。

方法

使用这种成熟的致癌物诱导的小鼠模型,我们研究了各种 ALT-803 给药方案(单独 SQ、SQ 联合膀胱内 BCG、单独膀胱内、膀胱内联合膀胱内 BCG)与单独膀胱内 BCG(阳性对照)和 PBS(阴性对照)相比的效果。作为肿瘤质量替代物的膀胱重量差异的非劣效性边界定义为 7%。

结果

所有治疗组(即,单独 SQ 的 ALT-803、SQ 联合膀胱内 BCG 的 ALT-803、单独膀胱内的 ALT-803、膀胱内联合膀胱内 BCG 的 ALT-803 和单独膀胱内 BCG)均显示肿瘤负担显著减轻,表现在膀胱重量和 H&E 染色上(p<0.005)。膀胱内 BCG 单独组与其他治疗组之间的非劣效性检验表明,单独 SQ 的 ALT-803(p=0.04)和 BCG 加 SQ 的 ALT-803(p=0.009)与膀胱内 BCG 单独治疗相当。在该模型中,我们未观察到 CD4 T、CD8 T 或 CD161/KLRB1 自然杀伤(NK)细胞在膀胱/肿瘤中的明显浸润。当评估外周血单核细胞时,单独 SQ 的 ALT-803 导致 CD8 T 细胞(p<0.01)、NKG2D NK 细胞(p<0.005)和 CD3/NKG2D NKT 细胞(p<0.005)的强烈诱导,而在脾组织中,单独 SQ 的 ALT-803 导致 CD3/NKG2D NKT 细胞(p<0.005)的强烈诱导与其他组相比。

结论

单独皮下 ALT-803 治疗或与膀胱内 BCG 联合治疗耐受良好,且不劣于单独膀胱内 BCG。CD8 T、NKG2D NK 和 CD3/NKG2D NKT 细胞的诱导以及关键细胞因子的诱导仍然是 ALT-803 的坚定机制。BCG 和 ALT-803 联合应用,无论是皮下给药还是膀胱内给药,其治疗指数均有所提高,这为进一步开发这些方案提供了有力依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dc1/6337786/8e0dca9731ee/12967_2019_1778_Fig1_HTML.jpg

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