临床与实验病理学杂志
臨床與實驗病理學雜誌
림상여실험병이학잡지
CHINESE JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY
2014年
9期
1016-1020,1025
,共6页
吕艺%刘茜%赵敏%陆江阳
呂藝%劉茜%趙敏%陸江暘
려예%류천%조민%륙강양
酵母多糖%脓毒症%树突状细胞%T淋巴细胞%程序性死亡受体配体-1
酵母多糖%膿毒癥%樹突狀細胞%T淋巴細胞%程序性死亡受體配體-1
효모다당%농독증%수돌상세포%T림파세포%정서성사망수체배체-1
zymosan%sepsis%splenic dendritic cell%T lymphocyte%PD-L1
目的:探讨酵母多糖致伤小鼠脓毒症病程发展过程中脾脏耐受性树突状细胞( dendritic cell, DC)的形成对脾脏T淋巴细胞免疫活性的影响,并通过程序性死亡受体-1(programmed death-1,PD-L1)抗体阻断PD-L1/PD-1途径改善耐受性DC对T淋巴细胞活性的抑制作用。方法采用酵母多糖腹腔注射的方法复制小鼠脓毒症模型。用磁珠法分离致伤小鼠脾脏DC和T淋巴细胞,测定脾脏组织中DC上PD-1、PD-L1、PIR-B的表达水平和分泌IL-12、IL-10的能力;检测脾脏T淋巴细胞增殖活性和IL-2的分泌水平。进一步将致伤组小鼠脾脏DC与正常小鼠脾脏T淋巴细胞混合培养,并加入PD-L1抗体,检测T淋巴细胞增殖活性及混合培养上清中IL-2、IL-12和IL-10含量。结果酵母多糖致伤后5天和12天组小鼠脾脏DC上PD-1、PD-L1及PIR-B的表达大幅上调,IL-12p70分泌减少,IL-12p40和IL-10分泌增加;脾脏T淋巴细胞增殖活性降低、IL-2分泌减少。在致伤组DC与正常T淋巴细胞混合培养体系中加入PD-L1抗体可减轻致伤组DC对T淋巴细胞增殖活性和分泌IL-2的抑制作用,并改善DC上IL-12p70、IL-12p40和IL-10的分泌能力。结论酵母多糖诱导小鼠脓毒症的病程晚期,脾脏耐受性DC的形成导致T淋巴细胞活性降低;PD-L1抗体通过干预PD-1/PD-L1途径改善T淋巴细胞和DC的免疫活性。
目的:探討酵母多糖緻傷小鼠膿毒癥病程髮展過程中脾髒耐受性樹突狀細胞( dendritic cell, DC)的形成對脾髒T淋巴細胞免疫活性的影響,併通過程序性死亡受體-1(programmed death-1,PD-L1)抗體阻斷PD-L1/PD-1途徑改善耐受性DC對T淋巴細胞活性的抑製作用。方法採用酵母多糖腹腔註射的方法複製小鼠膿毒癥模型。用磁珠法分離緻傷小鼠脾髒DC和T淋巴細胞,測定脾髒組織中DC上PD-1、PD-L1、PIR-B的錶達水平和分泌IL-12、IL-10的能力;檢測脾髒T淋巴細胞增殖活性和IL-2的分泌水平。進一步將緻傷組小鼠脾髒DC與正常小鼠脾髒T淋巴細胞混閤培養,併加入PD-L1抗體,檢測T淋巴細胞增殖活性及混閤培養上清中IL-2、IL-12和IL-10含量。結果酵母多糖緻傷後5天和12天組小鼠脾髒DC上PD-1、PD-L1及PIR-B的錶達大幅上調,IL-12p70分泌減少,IL-12p40和IL-10分泌增加;脾髒T淋巴細胞增殖活性降低、IL-2分泌減少。在緻傷組DC與正常T淋巴細胞混閤培養體繫中加入PD-L1抗體可減輕緻傷組DC對T淋巴細胞增殖活性和分泌IL-2的抑製作用,併改善DC上IL-12p70、IL-12p40和IL-10的分泌能力。結論酵母多糖誘導小鼠膿毒癥的病程晚期,脾髒耐受性DC的形成導緻T淋巴細胞活性降低;PD-L1抗體通過榦預PD-1/PD-L1途徑改善T淋巴細胞和DC的免疫活性。
목적:탐토효모다당치상소서농독증병정발전과정중비장내수성수돌상세포( dendritic cell, DC)적형성대비장T림파세포면역활성적영향,병통과정서성사망수체-1(programmed death-1,PD-L1)항체조단PD-L1/PD-1도경개선내수성DC대T림파세포활성적억제작용。방법채용효모다당복강주사적방법복제소서농독증모형。용자주법분리치상소서비장DC화T림파세포,측정비장조직중DC상PD-1、PD-L1、PIR-B적표체수평화분비IL-12、IL-10적능력;검측비장T림파세포증식활성화IL-2적분비수평。진일보장치상조소서비장DC여정상소서비장T림파세포혼합배양,병가입PD-L1항체,검측T림파세포증식활성급혼합배양상청중IL-2、IL-12화IL-10함량。결과효모다당치상후5천화12천조소서비장DC상PD-1、PD-L1급PIR-B적표체대폭상조,IL-12p70분비감소,IL-12p40화IL-10분비증가;비장T림파세포증식활성강저、IL-2분비감소。재치상조DC여정상T림파세포혼합배양체계중가입PD-L1항체가감경치상조DC대T림파세포증식활성화분비IL-2적억제작용,병개선DC상IL-12p70、IL-12p40화IL-10적분비능력。결론효모다당유도소서농독증적병정만기,비장내수성DC적형성도치T림파세포활성강저;PD-L1항체통과간예PD-1/PD-L1도경개선T림파세포화DC적면역활성。
Purpose To investigate the effect of tolerogenic dendritic cells ( DC) on T lymphocytes in the spleen during the develop-ment of zymosan-induced sepsis in mice, and to explore whether PD-L1 blockade could alleviate the immunosuppressive effect of tolero-genic DC on T lymphocytes. Methods Mice sepsis model was established by intraperitoneal injection of zymosan. Splenic DC and T lymphocytes were isolated respectively by using anti-CD11c and anti-CD3 magnetic beads. The expressions of PD-L1, PD-1 and PIR-B on splenic DC were measured, and IL-12 and IL-10 secreted from DC were determined. Mitogen-induced T lymphocyte proliferation and IL-2 secretion were assessed. Anti- PD-L1 antibody was added into mixed culture of tolerogenic DCs with normal Tcells. T cell proliferation and IL-2, IL-12 and IL-10 concentrations in the supernatant of mixed culture were determined. Results At 5 days and 12 days after zymosan injection, the expressions of PD-L1, PD-1 and PIR-B on splenic DC increased greatly, secretion of IL-12p70 re-duced and that of IL-12p40 and IL-10 augmented in DC, which were associated with decrease of T cells proliferation and IL-2 secre-tion. Administrating anti-PD-L1 antibody into the mixed culture of tolerogenic DC and Tcell could alleviate the suppression of DC on T lymphocyte proliferation and secretion of IL-2, and ameliorate the ability of DC secreting IL-12 and IL-10 as well. Conclusions At late stage of zymosan-induced sepsis, the formation of splenic tolerogenic DC resulted in immunosuppression of T lymphocytes. Anti-PD-L1 antibody could improve the immunoactivity of DC and T lymphocyte through intervening PD-L1/PD-1 pathway.