CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES >
Research progress of immune regulation protein B7 family on immune regulation during Schistosoma japonicum infection
Received date: 2022-05-11
Revised date: 2022-06-13
Online published: 2022-12-26
Supported by
National Natural Science Foundation of China(82172295);National Natural Science Foundation of China(81871677)
Schistosomiasis japonica is one of the most serious zoonotic diseases in the world. After schistosome infection, Th1 cells secrete interferon-γ (IFN-γ), tumour necrosis factor-α (TNF-α), and CD8+ T cells exert cellular immunity at the early stage. Th2 cells secrete a large amount of interleukin-4 (IL-4), interleukin-13 (IL-13) and interleukin-12 (IL-12), and the function of Th1 cells is inhibited in the later stage, thus prompting the host to produce an adaptive immune response dominated by humoral immunity. The B7 family is a secondary signal of T cell activation and plays a crucial role in regulating T cell immune responses. Further studies demonstrate that B7 family contains B7-1, B7-2, B7 homologue1 (B7-H1), B7 dendritic cell molecule (B7-DC), B7-H2, B7-H3, B7-H4, B7-H5, B7-H6 and B7-H7, which have costimulatory or coinhibitory effects on T cells. Some of them play an important role in immune regulation in schistosomiasis and the research progress of the B7 family in the immune regulation during schistosome infection is summarised in this paper.
Key words: Schistosoma japonicum; B7 family; Immune regulation
CHEN Guo , ZHU Dan-dan , DUAN Yi-nong . Research progress of immune regulation protein B7 family on immune regulation during Schistosoma japonicum infection[J]. CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES, 2022 , 40(6) : 774 -779 . DOI: 10.12140/j.issn.1000-7423.2022.06.013
| [1] | Hong Y, Fu Z, Cao X, et al. Changes in microRNA expression in response to Schistosoma japonicum infection[J]. Parasite Immunol, 2017, 39(2): e12416. |
| [2] | Chen QL, Zhang JQ, Zheng T, et al. The role of microRNAs in the pathogenesis, grading and treatment of hepatic fibrosis in schistosomiasis[J]. Parasit Vectors, 2019, 12(1): 611. |
| [3] | Sica GL, Choi IH, Zhu GF, et al. B7-H4, a molecule of the B7 family, negatively regulates T cell immunity[J]. Immunity, 2003, 18(6): 849-861. |
| [4] | Zhou S, Jin X, Li YL, et al. Blockade of PD-1 signaling enhances Th2 cell responses and aggravates liver immunopathology in mice with schistosomiasis japonica[J]. PLoS Negl Trop Dis, 2016, 10(10): e0005094. |
| [5] | McRae KM, Stear MJ, Good B, et al. The host immune response to gastrointestinal nematode infection in sheep[J]. Parasite Immunol, 2015, 37(12): 605-613. |
| [6] | Li QT, Qiu MJ, Yang SL, et al. Alpha-fetoprotein regulates the expression of immune-related proteins through the NF-κB (P65) pathway in hepatocellular carcinoma cells[J]. J Oncol, 2020, 2020: 9327512. |
| [7] | MacGregor HL, Ohashi PS. Molecular pathways: evaluating the potential for B7-H4 as an immunoregulatory target[J]. Clin Cancer Res, 2017, 23(12): 2934-2941. |
| [8] | Ahangar NK, Hemmat N, Khalaj-Kondori M, et al. The regulatory cross-talk between microRNAs and novel members of the B7 family in human diseases: a scoping review[J]. Int J Mol Sci, 2021, 22(5): 2652. |
| [9] | Zhu HF, Li Y. Small-molecule targets in tumor immunotherapy[J]. Nat Prod Bioprospect, 2018, 8(4): 297-301. |
| [10] | Wikenheiser DJ, Stumhofer JS. ICOS co-stimulation: friend or foe?[J]. Front Immunol, 2016, 7: 304. |
| [11] | Mach P, K?ninger A, Reisch B, et al. Soluble PD-L1 and B7-H4 serum levels during the course of physiological pregnancy[J]. Am J Reprod Immunol, 2022, 87(3): e13519. |
| [12] | Janakiram M, Chinai JM, Fineberg S, et al. Expression, clinical significance, and receptor identification of the newest B7 family member HHLA2 protein[J]. Clin Cancer Res, 2015, 21(10): 2359-2366. |
| [13] | Esensten JH, Helou YA, Chopra G, et al. CD28 costimulation: From mechanism to therapy[J]. Immunity, 2016, 44(5): 973-988. |
| [14] | Linsley PS, Brady W, Grosmaire L, et al. Binding of the B cell activation antigen B7 to CD28 costimulates T cell proliferation and interleukin 2 mRNA accumulation[J]. J Exp Med, 1991, 173(3): 721-730. |
| [15] | Hosseini A, Gharibi T, Marofi F, et al. CTLA-4: from mechanism to autoimmune therapy[J]. Int Immunopharmacol, 2020, 80: 106221. |
| [16] | Linsley PS, Brady W, Urnes M, et al. CTLA-4 is a second receptor for the B cell activation antigen B7[J]. J Exp Med, 1991, 174(3): 561-569. |
| [17] | Kraehenbuehl L, Weng CH, Eghbali S, et al. Enhancing immunotherapy in cancer by targeting emerging immunomodulatory pathways[J]. Nat Rev Clin Oncol, 2022, 19(1): 37-50. |
| [18] | Tian F, Xia CM, Luo W, et al. Effects of B7 costimulatory molecules on Th1/Th2 cytokine expression levels in the mice infected with Schistosoma japonicum[J]. J Trop Med, 2003, 3(2): 139-141, 206. (in Chinese) |
| (田芳, 夏超明, 骆伟, 等. 协同刺激分子B7-1/2对日本血吸虫感染小鼠Th1/Th2细胞因子表达水平的影响[J]. 热带医学杂志, 2003, 3(2): 139-141, 206.) | |
| [19] | Reiser H, Stadecker MJ. Costimulatory B7 molecules in the pathogenesis of infectious and autoimmune diseases[J]. N Engl J Med, 1996, 335(18): 1369-1377. |
| [20] | Subramanian G, Kazura JW, Pearlman E, et al. B7-2 requirement for helminth-induced granuloma formation and CD4 type 2 T helper cell cytokine expression[J]. J Immunol, 1997, 158(12): 5914-5920. |
| [21] | Simpson TR, Quezada SA, Allison JP. Regulation of CD4 T cell activation and effector function by inducible costimulator (ICOS)[J]. Curr Opin Immunol, 2010, 22(3): 326-332. |
| [22] | Nurieva RI, Duong J, Kishikawa H, et al. Transcriptional regulation of Th2 differentiation by inducible costimulator[J]. Immunity, 2003, 18(6): 801-811. |
| [23] | Yang Q, Qu JL, Jin CX, et al. Schistosoma japonicum infection promotes the response of Tfh cells through down-regulation of caspase-3-mediating apoptosis[J]. Front Immunol, 2019, 10: 2154. |
| [24] | Wang B, Liang S, Wang Y, et al. Th17 down-regulation is involved in reduced progression of schistosomiasis fibrosis in ICOSL KO mice[J]. PLoS Negl Trop Dis, 2015, 9(1): e0003434. |
| [25] | Chen XJ, Yang XW, Li Y, et al. Follicular helper T cells promote liver pathology in mice during Schistosoma japonicum infection[J]. PLoS Pathog, 2014, 10(5): e1004097. |
| [26] | Zhan TZ, Ma HH, Zhang TT, et al. Relation between ICOS signaling and Th9 cell polarization in mice infected with Schistosoma japonicum[J]. Chin J Schisto Control, 2018, 30(4): 436-439. (in Chinese) |
| (战廷正, 马会会, 张婷婷, 等. ICOS信号与日本血吸虫感染小鼠Th9细胞极化的关系[J]. 中国血吸虫病防治杂志, 2018, 30(4): 436-439.) | |
| [27] | Mak TW, Shahinian A, Yoshinaga SK, et al. Costimulation through the inducible costimulator ligand is essential for both T helper and B cell functions in T cell-dependent B cell responses[J]. Nat Immunol, 2003, 4(8): 765-772. |
| [28] | Heizmann B, Kastner P, Chan SS. The Ikaros family in lymphocyte development[J]. Curr Opin Immunol, 2018, 51: 14-23. |
| [29] | Wang Y, Cai R, Wang B, et al. Effects of Schistosoma japonicum infection on the CD28/CD86 signaling pathway and Th1/Th2 polarization in ICOS transgenic mice[J]. J Chin Med Univ, 2013, 42(6): 493-500. (in Chinese) |
| (王瑜, 蔡茹, 王波, 等. ICOS转基因小鼠感染日本血吸虫对CD28/CD86表达及Th1/Th2极化的影响[J]. 中国医科大学学报, 2013, 42(6): 493-500.) | |
| [30] | van der Vlugt LEPM, Obieglo K, Ozir-Fazalalikhan A, et al. Schistosome-induced pulmonary B cells inhibit allergic airway inflammation and display a reduced Th2-driving function[J]. Int J Parasitol, 2017, 47(9): 545-554. |
| [31] | Xu L, Qian X, Jin J, et al. Sex bias in generation and functional phenotypes of peripheral T follicular helper cells in schistosomiasis japonica[J]. Chin J Schisto Control, 2016, 28(2): 167-171. (in Chinese) |
| (许磊, 钱香, 金姣, 等. 性别对日本血吸虫感染过程中滤泡辅助性T细胞比例和活性影响的初步分析[J]. 中国血吸虫病防治杂志, 2016, 28(2): 167-171.) | |
| [32] | Zhang YM, Jiang YY, Wang YJ, et al. Higher frequency of circulating PD-1highCXCR5+CD4+ Tfh cells in patients with chronic schistosomiasis[J]. Int J Biol Sci, 2015, 11(9): 1049-1055. |
| [33] | Xie SH, Wei HX, Peng AP, et al. Ikzf2 regulates the development of ICOS+ Th cells to mediate immune response in the spleen of S. japonicum-infected C57BL/6 mice[J]. Front Immunol, 2021, 12: 687919. |
| [34] | Xia CM, Pu XK, Gong W, et al. Immune response and immunopathology in inducible costimulatory molecule(ICOS) transgenic mice infected with Schistosoma japonicum[J]. Chin J Parasitol Parasit Dis, 2006, 24(5): 349-352. (in Chinese) |
| 夏超明, 濮翔科, 龚唯, 等. 日本血吸虫感染可诱导共刺激分子(ICOS)转基因小鼠的免疫应答及其病理反应[J]. 中国寄生虫学与寄生虫病杂志, 2006, 24(5): 349-352.) | |
| [35] | Wang YY, Lin C, Cao Y, et al. Up-regulation of interleukin-21 contributes to liver pathology of schistosomiasis by driving GC immune responses and activating HSCs in mice[J]. Sci Rep, 2017, 7(1): 16682. |
| [36] | Delmas D, Hermetet F, Aires V. PD-1/PD-L1 checkpoints and resveratrol: a controversial new way for a therapeutic strategy[J]. Cancers (Basel), 2021, 13(18): 4509. |
| [37] | Sharpe AH, Pauken KE. The diverse functions of the PD1 inhibitory pathway[J]. Nat Rev Immunol, 2018, 18(3): 153-167. |
| [38] | Smith P, Walsh CM, Mangan NE, et al. Schistosoma mansoni worms induce anergy of T cells via selective up-regulation of programmed death ligand 1 on macrophages[J]. J Immunol, 2004, 173(2): 1240-1248. |
| [39] | Zhang YM, Wu YL, Liu H, et al. Granulocytic myeloid-derived suppressor cells inhibit T follicular helper cells during experimental Schistosoma japonicum infection[J]. Parasites Vectors, 2021, 14(1): 497. |
| [40] | Gao YN, Chen L, Hou M, et al. TLR2 directing PD-L2 expression inhibit T cells response in Schistosoma japonicum infection[J]. PLoS One, 2013, 8(12): e82480. |
| [41] | Khan AR, Hams E, Floudas A, et al. PD-L1hi B cells are critical regulators of humoral immunity[J]. Nat Commun, 2015, 6: 5997. |
| [42] | Zhang Y, Morgan R, Chen C, et al. Mammary-tumor-educated B cells acquire LAP/TGF-β and PD-L1 expression and suppress anti-tumor immune responses[J]. Int Immunol, 2016, 28(9): 423-433. |
| [43] | Xiao JL, Guan F, Sun L, et al. B cells induced by Schistosoma japonicum infection display diverse regulatory phenotypes and modulate CD4+ T cell response[J]. Parasit Vectors, 2020, 13(1): 147. |
| [44] | Feng RR, Chen Y, Liu Y, et al. The role of B7-H3 in tumors and its potential in clinical application[J]. Int Immunopharmacol, 2021, 101: 108153. |
| [45] | Nagai S, Azuma M. The CD28-B7 family of co-signaling molecules[J]. Adv Exp Med Biol, 2019, 1189: 25-51. |
| [46] | Ueno T, Yeung MY, McGrath M, et al. Intact B7-H3 signaling promotes allograft prolongation through preferential suppression of Th1 effector responses[J]. Eur J Immunol, 2012, 42(9): 2343-2353. |
| [47] | Liu F, Zhang T, Zou ST, et al. B7-H3 promotes cell migration and invasion through the Jak2/Stat3/MMP9 signaling pathway in colorectal cancer[J]. Mol Med Rep, 2015, 12(4): 5455-5460. |
| [48] | Li YC, Guo GN, Song J, et al. B7-H3 promotes the migration and invasion of human bladder cancer cells via the PI3K/Akt/STAT3 signaling pathway[J]. J Cancer, 2017, 8(5): 816-824. |
| [49] | Li SX, Zhang GB, Sun HH, et al. Establishment of a sandwich ELISA for testing serum SB7-H3 and detection of SB7-H3 levels in liver disease[J]. Chin J Cell Mol Immunol, 2012, 28(1): 84-86, 90. (in Chinese) |
| (李淑湘, 张光波, 孙海洪, 等. 人可溶性B7-H3酶联试剂盒的研制及在肝病患者血清中水平的检测[J]. 细胞与分子免疫学杂志, 2012, 28(1): 84-86, 90.) |
/
| 〈 |
|
〉 |