• 中国中文核心期刊
  • 中国科学引文数据库核心期刊
  • 中国科技核心期刊
  • 中国高校百佳科技期刊
高级检索

PD-L1疫苗中引入不同免疫原性氨基酸对T细胞亚群分化的影响

陈红梅, 康彦良, 刘利, 姚文兵, 田浤

陈红梅, 康彦良, 刘利, 姚文兵, 田浤. PD-L1疫苗中引入不同免疫原性氨基酸对T细胞亚群分化的影响[J]. 中国药科大学学报, 2020, 51(3): 349-356. DOI: 10.11665/j.issn.1000-5048.20200313
引用本文: 陈红梅, 康彦良, 刘利, 姚文兵, 田浤. PD-L1疫苗中引入不同免疫原性氨基酸对T细胞亚群分化的影响[J]. 中国药科大学学报, 2020, 51(3): 349-356. DOI: 10.11665/j.issn.1000-5048.20200313
CHEN Hongmei, KANG Yanliang, LIU Li, YAO Wenbing, TIAN Hong. Effects of different immunogenic amino acids in PD-L1 vaccine on the differentiation of T cell subsets[J]. Journal of China Pharmaceutical University, 2020, 51(3): 349-356. DOI: 10.11665/j.issn.1000-5048.20200313
Citation: CHEN Hongmei, KANG Yanliang, LIU Li, YAO Wenbing, TIAN Hong. Effects of different immunogenic amino acids in PD-L1 vaccine on the differentiation of T cell subsets[J]. Journal of China Pharmaceutical University, 2020, 51(3): 349-356. DOI: 10.11665/j.issn.1000-5048.20200313

PD-L1疫苗中引入不同免疫原性氨基酸对T细胞亚群分化的影响

基金项目: 国家自然科学基金资助项目(No. 81573222, No. 81673343, No. 91753112)

Effects of different immunogenic amino acids in PD-L1 vaccine on the differentiation of T cell subsets

Funds: This study was supported by the National Natural Science Foundation of China (No. 81973222, No.81673343, No.91753112)
  • 摘要: 为了比较内源性的3-硝基酪氨酸与非天然的4-硝基苯丙氨酸在PD-L1疫苗中的引入对T细胞亚群分化的影响,利用遗传密码扩充技术,将这两种免疫原性氨基酸分别引入到PD-L1疫苗的相同位点,获得具有3-硝基酪氨酸以及4-硝基苯丙氨酸的两种PD-L1突变体。用这两种突变体免疫小鼠,分析对小鼠脾脏T细胞亚群分化的影响。流式细胞术检测结果显示,4-硝基苯丙氨酸在PD-L1疫苗中的引入可促进Th1细胞的极化,同时降低Treg细胞的比例,3-硝基酪氨酸的引入对Th1细胞的极化无影响,同时能显著提高Treg和Th17细胞的比例。二者在PD-L1疫苗中的引入均能促进脾脏CD8+ T细胞的应答,其中含有4-硝基苯丙氨酸的PD-L1突变体应答效果更强。实验结果表明,与内源性的3-硝基酪氨酸在PD-L1疫苗中的引入相比,非天然的4-硝基苯丙氨酸更适合用于肿瘤疫苗的设计。
    Abstract: To compare the effects of endogenous 3-nitrotyrosine and non-natural 4-nitrophenylalanine in PD-L1 vaccine on the differentiation of T cell subsets, two immunogenic amino acids were introduced into the same site of PD-L1 vaccine. Two PD-L1 mutants with 3-nitrotyrosine and 4-nitrophenylalanine were obtained, respectively, using genetic code expansion technology. Mice were immunized with these two mutants, and their effects on the differentiation of T cell subsets in spleen were analyzed. The results of flow cytometry showed that the introduction of 4-nitrophenylalanine in PD-L1 vaccine could promote the polarization of Th1 cells while reducing the proportion of Treg cells; the introduction of 3-nitrotyrosine had no effect on the polarization of Th1 cells, while significantly increasing the proportion of Treg and Th17 cells. The introduction of both into PD-L1 vaccine could promote the response of CD8+ T cells in spleen, and the response of PD-L1 mutant containing 4-nitrophenylalanine was stronger. In summary, the non-natural 4-nitrophenylalanine is more suitable for the design of tumor vaccines as compared with endogenous 3-nitrotyrosine.
  • [1] . Proc Natl Acad Sci U S A, 2008, 105(32): 11276-11280.
    [2] Grünewald J, Hunt GS, Dong L, et al. Mechanistic studies of the immunochemical termination of self-tolerance with unnatural amino acids[J]. Proc Natl Acad Sci U S A, 2009, 106(11): 4337-4342.
    [3] Khan F, Siddiqui AA. Prevalence of anti-3-nitrotyrosine antibodies in the joint synovial fluid of patients with rheumatoid arthritis, osteoarthritis and systemic lupus erythematosus[J]. Clin Chim Acta, 2006, 370(1/2): 100-107.
    [4] Khan F, Ali R. Antibodies against nitric oxide damaged poly L-tyrosine and 3-nitrotyrosine levels in systemic lupus erythematosus[J]. J Biochem Mol Biol, 2006, 39(2): 189-196.
    [5] Thomson L, Christie J, Vadseth C, et al. Identification of immunoglobulins that recognize 3-nitrotyrosine in patients with acute lung injury after major trauma[J]. Am J Respir Cell Mol Biol, 2007, 36(2): 152-157.
    [6] Ohmori H, Kanayama N. Immunogenicity of an inflammation-associated product, tyrosine nitrated self-proteins[J]. Autoimmun Rev, 2005, 4(4): 224-229.
    [7] Hardy LL, Wick DA, Webb JR. Conversion of tyrosine to the inflammation-associated analog 3''''-nitrotyrosine at either TCR- or MHC-contact positions can profoundly affect recognition of the MHC class I-restricted epitope of lymphocytic choriomeningitis virus glycoprotein 33 by CD8 T cells[J]. J Immunol, 2008, 180(9): 5956-5962.
    [8] He Y, Tian H, Dai X, et al. Immunogenicity of HER2 vaccine containing p-nitrophenylalanine[J]. J China Pharm Univ (中国药科大学学报), 2018, 49(3): 369-375.
    [9] Tian H, He Y, Song XD, et al. Nitrated T helper cell epitopes enhance the immunogenicity of HER2 vaccine and induce anti-tumor immunity[J]. Cancer Lett, 2018, 430: 79-87.
    [10] Tian H, Kang YL, Song XD, et al. PDL1-targeted vaccine exhibits potent antitumor activity by simultaneously blocking PD1/PDL1 pathway and activating PDL1-specific immune responses[J]. Cancer Lett, 2020, 476: 170-182.
    [11] Datta J, Fracol M, McMillan MT, et al. Association of depressed anti-HER2 T-helper type 1 response with recurrence in patients with completely treated HER2-positive breast cancer: role for immune monitoring[J]. JAMA Oncol, 2016, 2(2): 242-246.
    [12] Antony PA, Piccirillo CA, Akpinarli A, et al. CD8+ T cell immunity against a tumor/self-antigen is augmented by CD4+ T helper cells and hindered by naturally occurring T regulatory cells[J]. J Immunol, 2005, 174(5): 2591-2601.
    [13] Lakshminrusimha S, Suresh MV, Knight PR, et al. Role of pulmonary artery reactivity and nitric oxide in injury and inflammation following lung contusion[J]. Shock, 2013, 39(3): 278-285.
    [14] Thomson L. 3-Nitrotyrosine modified proteins in atherosclerosis[J]. Dis Markers, 2015, 2015: 1-8.
    [15] Ferreira I, Croca S, Raimondo MG, et al. Nitrated nucleosome levels and neuropsychiatric events in systemic lupus erythematosus; a multi-center retrospective case-control study[J]. Arthritis Res Ther, 2017, 19(1): 287.
    [16] Jin B, Sun T, Yu XH, et al. The effects of TLR activation on T-cell development and differentiation[J]. Clin Dev Immunol, 2012, 2012: 836485.
    [17] Li P, Spolski R, Liao W, et al. Complex interactions of transcription factors in mediating cytokine biology in T cells[J]. Immunol Rev, 2014, 261(1): 141-156.
计量
  • 文章访问数:  214
  • HTML全文浏览量:  3
  • PDF下载量:  523
  • 被引次数: 0
出版历程
  • 收稿日期:  2020-03-22
  • 修回日期:  2020-05-07
  • 刊出日期:  2020-06-24

目录

    /

    返回文章
    返回
    x 关闭 永久关闭