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AASLD2020[855]ANTI-PD-1的管理时间对 增加AAV-HBV中的HBV特异性免疫 [复制链接]

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发表于 2020-11-1 09:49 |只看该作者 |倒序浏览 |打印
855
TIMING OF ADMINISTRATION OF ANTI-PD-1 IS IMPORTANT TO
INCREASE HBV-SPECIFIC IMMUNE RESPONSES IN AAV-HBV
MICE
Ben De Clerck1, Dorien De Pooter1, Wim Pierson2, Koen
Dockx2, Claire Evans3, Helen Horton4 and Ellen Van Gulck1,
(1)Infectious Diseases and Vaccines, J&J, (2)Charles River
Laboratories, (3)Ichor Medical Systems Inc, (4)Was Employed
By Janssen at the Time of the Study but Is No Longer Part of
the Company
Background: In chronic HBV-infected individuals,
HBV-specific immune responses are dysfunctional and
programmed cell death receptor (PD-1) is upregulated on
T-cells in periphery and liver The AAV-HBV infected mice
model was used to evaluate whether a therapeutic vaccine
can increase HBV-specific Immune responses and what
the best timing is to administer anti-PD-1 to enhance the
immunogenicity Methods: Male C57Bl/6JrJ mice, 6-8 weeks
old are infected with AAV-HBV for 28 days when chronicity
is reached All mice were vaccinated by electroporation
with pDF core and pDFpol on day 28 and on day 49 after
infection Anti-mouse PD-1 (10mg/kg) was administered on
the same time of vaccination, 1 day after the vaccination,
together with the last vaccination, 1 day after last vaccination
or 1 week after last vaccination Control mice were treated
with corresponding isotype antibody Mice were euthanized
2 weeks after last vaccination, splenocytes and intrahepatic
lymphocytes (IHL) were isolated and used in assays to
evaluate immune responses Viral parameters and ALT levels
are followed during the treatment procedure Results: Mice
treated with the therapeutic vaccine induced both splenic and
intrahepatic functional T-cells, although more than 10% of
the IHL express PD-1 on their CD8 T-cells The proliferation
capacity of intrahepatic T-cells was significantly enhanced
when anti-PD-1 was administered 1 week after the second
vaccination No effect on viral parameters could be detected
No other treatment regimens induced a significant effect
on functionality of T-cells Conclusion: Herein it is showed
that administration of anti-PD-1 one week after therapeutic
vaccination can improve the functionality of intrahepatic
lymphocytes in AAV-HBV infected mice To see an effect on
viral parameters this vaccination strategy should be combined
with agents lowering HBV s-antigen.

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发表于 2020-11-1 09:50 |只看该作者
855
ANTI-PD-1的管理时间对
增加AAV-HBV中的HBV特异性免疫反应
老鼠
Ben De Clerck1,Dorien De Pooter1,Wim Pierson2,科恩
Dockx2,Claire Evans3,Helen Horton4和Ellen Van Gulck1,
(1)强生公司传染病和疫苗,(2)查尔斯河
实验室,(3)艾科医疗系统公司,(4)从业人员
Janssen在研究期间,但已不再是该研究的一部分
公司
背景:在慢性HBV感染者中,
HBV特异性免疫反应异常
程序性细胞死亡受体(PD-1)上调
外周和肝脏中的T细胞AAV-HBV感染的小鼠
模型用于评估治疗性疫苗是否
可以增加特定于HBV的免疫反应以及
最佳时机是施用抗PD-1来增强
免疫原性方法:雄性C57Bl / 6JrJ小鼠,6-8周
慢性时,老年人被AAV-HBV感染28天
达到所有小鼠通过电穿孔接种疫苗
在第28天和之后的第49天使用pDF core和pDFpol
感染给予抗小鼠PD-1(10mg / kg)
接种同一天,接种后1天,
最后一次疫苗接种,最后一次疫苗接种后1天
或最后一次疫苗接种后1周
带有相应的同种型抗体的小鼠被安乐死
上次疫苗接种后2周,脾细胞和肝内
分离出淋巴细胞(IHL)并用于检测
评估免疫反应病毒参数和ALT水平
在治疗过程中被跟踪结果:小鼠
用治疗性疫苗诱导的脾脏和
肝内功能性T细胞,尽管超过10%
IHL在其CD8 T细胞上表达PD-1
肝内T细胞的能力明显增强
第二次注射1周后给予抗PD-1
疫苗接种对病毒参数没有影响
没有其他治疗方案能产生明显的作用
结论:在此显示
治疗后一周服用抗PD-1
接种疫苗可以改善肝内功能
感染AAV-HBV的小鼠体内的淋巴细胞
病毒参数应结合此疫苗接种策略
降低HBV S抗原的药物。
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