中国防痨杂志 ›› 2026, Vol. 48 ›› Issue (9): 1428-1435.doi: 10.19982/j.issn.1000-6621.20250531
赵萌, 阿卜杜萨拉木·阿力木江, 王茜, 张俊, 徐子逸, 廖俊儒, 马创(
)
收稿日期:2025-12-29
出版日期:2026-09-10
发布日期:2026-09-08
通信作者:
马创
E-mail:1516175919@qq.com
基金资助:
Zhao Meng, Abdusalam Alimujiang, Wang Xi, Zhang Jun, Xu Ziyi, Liao Junru, Ma Chuang(
)
Received:2025-12-29
Online:2026-09-10
Published:2026-09-08
Contact:
Ma Chuang
E-mail:1516175919@qq.com
Supported by:摘要:
布鲁氏菌病是由布鲁氏菌侵入机体引起的一种人畜共患的自然疫源性传染病,在全球范围内广泛分布。布鲁氏菌病具有显著的全身侵袭性,可累及多个系统,其中骨关节系统损害是最常见的并发症之一。布鲁氏菌导致骨关节系统损害的具体发病机制仍未完全阐明,并且由于早期临床症状及影像学表现不典型,使得临床诊疗面临重大挑战。多数患者明确诊断时病情已进展至晚期阶段,此时骨组织遭受严重破坏,引起灾难性的功能丧失和生活质量急剧下降。因此为提高临床工作者对布鲁氏菌导致骨关节系统损害的认识及重视程度,作者从布鲁氏菌对成骨、破骨和骨细胞的致病机制入手,对布鲁氏菌导致骨关节系统损害的机制进行综述,以期为该病的研究及治疗提供新的思路和方向。
中图分类号:
赵萌, 阿卜杜萨拉木·阿力木江, 王茜, 张俊, 徐子逸, 廖俊儒, 马创. 布鲁氏菌导致骨组织细胞损害的机制研究进展[J]. 中国防痨杂志, 2026, 48(9): 1428-1435. doi: 10.19982/j.issn.1000-6621.20250531
Zhao Meng, Abdusalam Alimujiang, Wang Xi, Zhang Jun, Xu Ziyi, Liao Junru, Ma Chuang. Research progress on the mechanisms of bone tissue cell damage caused by Brucella[J]. Chinese Journal of Antituberculosis, 2026, 48(9): 1428-1435. doi: 10.19982/j.issn.1000-6621.20250531
| [1] | GŁOwacka P, ŻAkowska D, Naylor K, et al. Brucella-Virulence Factors, Pathogenesis and Treatment[J]. Pol J Microbiol, 2018, 67(2): 151-161. doi:10.21307/pjm-2018-029. |
| [2] | Xiao Y, Li M, Guo X, et al. Inflammatory Mechanism of Brucella Infection in Placental Trophoblast Cells[J]. Int J Mol Sci, 2022, 23(21):13417. doi:10.3390/ijms232113417. |
| [3] | Bialer M G, Sycz G, González F M, et al. Adhesins of Brucella: Their Roles in the Interaction with the Host[J]. Pathogens, 2020, 9(11):942. doi:10.3390/pathogens9110942. |
| [4] | 崔步云. 中国布鲁氏菌病疫情监测与控制[J]. 疾病监测, 2007, 22(10):649-651. doi:10.3784/j.issn.1003-9961.2007.10.001. |
| [5] | Pappas G, Akritidis N, Bosilkovski M, et al. Brucellosis[J]. N Engl J Med, 2005, 352(22):2325-2336. doi:10.1056/NEJMra050570. |
| [6] | Dadar M, Al-Khaza’leh J, Fakhri Y, et al. Human brucellosis and associated risk factors in the Middle East region: A comprehensive systematic review, meta-analysis, and meta-regression[J]. Heliyon, 2024, 10(14):e34324. doi:10.1016/j.heliyon.2024.e34324. |
| [7] | Zhang S S, Zhang Y X, Lio W, et al. Uncertain Time Series Analysis for the Confirmed Case of Brucellosis in China[J]. Symmetry, 2024, 16(9):1160. doi:10.3390/sym16091160. |
| [8] |
Yanmaz B, Özgen E K, Sayi O, et al. Phylogenetic Analysis of Brucella melitensis Strains Isolated from Humans Using 16S rRNA Sequencing and Multiple Locus Variable Number of Tandem Repeats Analysis-16[J]. Vector Borne Zoonotic Dis, 2024, 24(7): 416-423. doi:10.1089/vbz.2023.0139.
pmid: 38608219 |
| [9] | Zhan T S, Li Y, Xie Y J, et al. Multiepitope fusion protein-based ELISA for enhanced brucellosis serodiagnosis[J]. PLoS Negl Trop Dis, 2025, 19(12):e0013804. doi:10.1371/journal.pntd.0013804. |
| [10] | Pritam M, Kumar R. Pathophysiology, Current Therapeutic Options, Vaccine Candidates, and Drug Targets for Human Brucellosis[J]. Curr Mol Pharmacol, 2024, 17:e130723218680. doi:10.2174/1874467217666230713093802. |
| [11] | Laine C G, Johnson V E, Scott H M, et al. Global Estimate of Human Brucellosis Incidence[J]. Emerg Infect Dis, 2023, 29(9): 1789-1797. doi:10.3201/eid2909.230052. |
| [12] | de Figueiredo P, Ficht T A, Rice-Ficht A, et al. Pathogenesis and Immunobiology of Brucellosis Review of Brucella-Host Interactions[J]. Am J Pathol, 2015, 185(6): 1505-1517. doi:10.1016/j.ajpath.2015.03.003. |
| [13] | Tian Z H, Wan L Y, Pei J, et al. Brucellosis seroprevalence in cattle in China during 2014-2024: a systematic review and meta-analysis[J]. Emerg Microbes Infect, 2024, 13(1): 2417859. doi:10.1080/22221751.2024.2417859. |
| [14] | 王登芹, 赵会丽, 张茜茜, 等. 布鲁氏菌病合并骨关节炎患者临床特征分析[J]. 中华地方病学杂志, 2024, 43(2): 137-140. doi:10.3760/cma.j.cn231583-20230515-00115. |
| [15] | Spernovasilis N, Karantanas A, Markaki I, et al. Spondylitis: Current Knowledge and Recent Advances[J]. J Clin Med, 2024, 13(2): 595. doi:10.3390/jcm13020595. |
| [16] | 安绪平, 张文杰, 杨晓娟. 布鲁氏杆菌病的感染部位及机制研究[J]. 医学信息, 2024, 37(11): 180-183. doi:10.3969/j.issn.1006-1959.2024.11.038. |
| [17] | 王猛, 姚五平, 柳直, 等. 关节镜辅助下关节腔滑膜清理术治疗布鲁氏菌感染后单侧膝骨关节炎2例报道[J]. 中华骨与关节外科杂志, 2025, 18(3):286-288. doi:10.3969/j.issn.2095-9958.2025.03.14. |
| [18] | 何雄, 郭辉. 布鲁氏菌骨关节病的研究进展[J]. 兵团医学, 2023, 21(2):50-52. doi:10.3969/j.issn.1672-4356.2023.02.026 |
| [19] | 赵旭, 牛克梅, 高霞, 等. 258例急性期和慢性期布鲁氏菌病患者临床表现、实验室特征及治疗效果比较[J]. 中国人兽共患病学报, 2025, 41(6):660-667. doi:10.3969/j.issn.1002-2694.2025.00.109. |
| [20] | Bolamperti S, Villa I, Rubinacci A. Bone remodeling: an operational process ensuring survival and bone mechanical competence[J]. Bone Res, 2022, 10(1):48. doi:10.1038/s41413-022-00219-8. |
| [21] | Zhu G Y, Zhang T X, Chen M, et al. Bone physiological microenvironment and healing mechanism: Basis for future bone-tissue engineering scaffolds[J]. Bioact Mater, 2021, 6(11): 4110-4140. doi:10.1016/j.bioactmat.2021.03.043. |
| [22] | Siddiqui J A, Partridge N C. Physiological Bone Remodeling: Systemic Regulation and Growth Factor Involvement[J]. Physiology (Bethesda), 2016, 31(3): 233-245. doi:10.1152/physiol.00061.2014. |
| [23] | 程鉥泺, 陶雪芬, 赵荣, 等. TLR4/NF-κB通路与骨质疏松症关系的研究进展[J]. 中国骨质疏松杂志, 2023, 29(7):1037-1042. doi:10.3969/j.issn.1006-7108.2023.07.020. |
| [24] | Delgado-Calle J, Bellido T. The osteocyte as a signaling cell[J]. Physiol Rev, 2022, 102(1):379-410. doi:10.1152/physrev.00043.2020. |
| [25] | Kitaura H, Marahleh A, Ohori F, et al. Osteocyte-Related Cytokines Regulate Osteoclast Formation and Bone Resorption[J]. Int J Mol Sci, 2020, 21(14): 5169. doi:10.3390/ijms21145169. |
| [26] | Yang J C, Dong D D, Luo X L, et al. Iron Overload-Induced Osteocyte Apoptosis Stimulates Osteoclast Differentiation Through Increasing Osteocytic RANKL Production In Vitro[J]. Calcif Tissue Int, 2020, 107(5): 499-509. doi:10.1007/s00223-020-00735-x. |
| [27] | Khalaf O H, Chaki S P, Garcia-Gonzalez D G, et al. The NOD-scid IL2rγnull Mouse Model Is Suitable for the Study of Osteoarticular Brucellosis and Vaccine Safety[J]. Infect Immun, 2019, 87(6):e00901-18. doi:10.1128/IAI.00901-18. |
| [28] | Khalaf O H, Chaki S P, Garcia-Gonzalez D G, et al. Interaction of Brucella abortus with Osteoclasts: a Step toward Understanding Osteoarticular Brucellosis and Vaccine Safety[J]. Infect Immun, 2020, 88(4): e00822-19. doi:10.1128/IAI.00822-19. |
| [29] |
Giambartolomei G H, Scian R, Acosta-Rodríguez E, et al. Brucella abortus-Infected Macrophages Modulate T Lymphocytes to Promote Osteoclastogenesis via IL-17[J]. Am J Pathol, 2012, 181(3): 887-896. doi:10.1016/j.ajpath.2012.05.029.
pmid: 22901753 |
| [30] |
Haynes D R. Bone lysis and inflammation[J]. Inflamm Res, 2004, 53(11): 596-600. doi:10.1007/s00011-004-1303-z.
pmid: 15693607 |
| [31] |
Ayelén Ivana P V, Paula Constanza A B, Guillermo Hernán G, et al. Brucella abortus-infected B cells induce osteoclastogenesis[J]. Microbes Infect, 2016, 18(9): 529-535. doi:10.1016/j.micinf.2016.04.001.
pmid: 27109230 |
| [32] |
Viglietti A I P, Benitez P C A, Gentilini M V, et al. Brucella abortus Invasion of Osteocytes Modulates Connexin 43 and Integrin Expression and Induces Osteoclastogenesis via Receptor Activator of NF-κB Ligand and Tumor Necrosis Factor Alpha Secretion[J]. Infect Immun, 2016, 84(1): 11-20. doi:10.1128/iai.01049-15.
pmid: 26459511 |
| [33] |
Giambartolomei G H, Benitez P C A, Delpino M V. Brucella and Osteoarticular Cell Activation: Partners in Crime[J]. Front Microbiol, 2017, 8:256. doi:10.3389/fmicb.2017.00256.
pmid: 28265268 |
| [34] | Andreev D, Liu M D, Weidner D, et al. Osteocyte necrosis triggers osteoclast-mediated bone loss through macrophage-inducible C-type lectin[J]. J Clin Invest, 2020, 130(9): 4811-4830. doi:10.1172/jci134214. |
| [35] | Kitase Y, Prideaux M. Targeting osteocytes vs osteoblasts[J]. Bone, 2023, 170:116724. doi:10.1016/j.bone.2023.116724. |
| [36] | Scian R, Barrionuevo P, Fossati C A, et al. Brucella abortus Invasion of Osteoblasts Inhibits Bone Formation[J]. Infect Immun, 2012, 80(7): 2333-2345. doi:10.1128/iai.00208-12. |
| [37] | Bialer M G, Ferrero M C, Delpino M V, et al. Adhesive Functions or Pseudogenization of Type Va Autotransporters in Brucella Species[J]. Front Cell Infect Microbiol, 2021, 11: 607610. doi:10.3389/fcimb.2021.607610. |
| [38] | 李江笔, 王永杰, 刘军, 等. 布鲁菌骨关节病发病机制的研究进展[J]. 中华地方病学杂志, 2019, 38(12): 1019-1022. doi:10.3760/cma.j.issn.2095-4255.2019.12.019. |
| [39] | Delpino M V, Fossati C A, Baldi P C. Proinflammatory Response of Human Osteoblastic Cell Lines and Osteoblast-Monocyte Interaction upon Infection with Brucella spp[J]. Infect Immun, 2009, 77(3): 984-995. doi:10.1128/iai.01259-08. |
| [40] | Scian R, Barrionuevo P, Giambartolomei G H, et al. Granulocyte-Macrophage Colony-Stimulating Factor- and Tumor Necrosis Factor Alpha-Mediated Matrix Metalloproteinase Production by Human Osteoblasts and Monocytes after Infection with Brucella abortus[J]. Infect Immun, 2011, 79(1): 192-202. doi:10.1128/iai.00934-10. |
| [41] |
Gentilini M V, Viglietti A I P, Benitez P C A, et al. Inhibition of Osteoblast Function by Brucella abortus is Reversed by Dehydroepiandrosterone and Involves ERK1/2 and Estrogen Receptor[J]. Front Immunol, 2018, 9:88. doi:10.3389/fimmu.2018.00088.
pmid: 29434601 |
| [42] | Viglietti A I P, Gentilini M V, Benitez P C A, et al. B.abortus Modulates Osteoblast Function Through the Induction of Autophagy[J]. Front Cell Infect Microbiol, 2018, 8: 425. doi:10.3389/fcimb.2018.00425. |
| [43] | Freiberger R N, López C A M, Sviercz F A, et al. B.abortus Infection Promotes an Imbalance in the Adipocyte-Osteoblast Crosstalk Favoring Bone Resorption[J]. Int J Mol Sci, 2023, 24(6): 5617. doi:10.3390/ijms24065617. |
| [44] | Pesce Viglietti A, Giambartolomei G, Quarleri J, et al. Brucella abortus Infection Modulates 3T3-L1 Adipocyte Inflammatory Response and Inhibits Adipogenesis[J]. Front Endocrinol (Lausanne), 2020, 11:585923. doi:10.3389/fendo.2020.585923. |
| [45] | Hua R, Truong V A, Fajardo R J, et al. Connexin hemichannels drive lactation-induced osteocyte acidification and perilacunar-canalicular remodeling[J]. Cell Rep, 2024, 43(7): 114363. doi:10.1016/j.celrep.2024.114363. |
| [46] |
Viglietti A I P, Giambartolomei G H, Delpino M V. Endocrine modulation of Brucella abortus-infected osteocytes function and osteoclastogenesis via modulation of RANKL/OPG[J]. Microbes Infect, 2019, 21(7): 287-295. doi:10.1016/j.micinf.2019.01.004.
pmid: 30735720 |
| [47] | Scian R, Barrionuevo P, Rodriguez A M, et al. Brucella abortus Invasion of Synoviocytes Inhibits Apoptosis and Induces Bone Resorption through RANKL Expression[J]. Infect Immun, 2013, 81(6): 1940-1951. doi:10.1128/iai.01366-12. |
| [48] | Scian R, Barrionuevo P, Giambartolomei G H, et al. Potential Role of Fibroblast-Like Synoviocytes in Joint Damage Induced by Brucella abortus Infection through Production and Induction of Matrix Metalloproteinases[J]. Infect Immun, 2011, 79(9): 3619-3632. doi:10.1128/iai.05408-11. |
| [49] | 地力牙尔·莫合塔尔, 李国庆, 纪保超, 等. 一期全髋人工关节置换术治疗晚期髋关节布氏杆菌关节炎的临床效果[J]. 中华外科杂志, 2019, 57(8): 629-631. doi:10.3760/cma.j.issn.0529-5815.2019.08.013. |
| [50] | 王城, 马臻. 99Tcm-MDP SPECT/CT诊断布鲁氏菌病脊柱炎[J]. 中国医学影像技术, 2022, 38(3):431-434. doi:10.13929/j.issn.1003-3289.2022.03.025. |
| [51] | 王艳, 杨豫新, 刘文亚, 等. 布鲁氏菌性骶髂关节炎MRI诊断[J]. 临床放射学杂志, 2019, 38(6):1090-1093. doi:10.13437/j.cnki.jcr.2019.06.034. |
| [52] | 秋叶红, 李静波, 李响, 等. 布鲁氏菌毒力因子及致病机制研究新进展[J]. 内蒙古民族大学学报(自然科学版), 2020, 35(5): 413-417. doi:10.14045/j.cnki.15-1220.2020.05.009. |
| [53] | Jiao H W, Zhou Z X, Li B W, et al. The Mechanism of Facultative Intracellular Parasitism of Brucella[J]. Int J Mol Sci, 2021, 22(7): 3673. doi:10.3390/ijms22073673. |
| [54] | Li J M, Qi L, Diao Z Y, et al. Brucella BtpB Manipulates Apoptosis and Autophagic Flux in RAW264.7 Cells[J]. Int J Mol Sci, 2022, 23(22): 14439. doi:10.3390/ijms232214439. |
| [55] | Gorvel J P. Brucella: a Mr “Hide” converted into Dr Jekyll[J]. Microbes Infect, 2008, 10(9): 1010-1013. doi:10.1016/j.micinf.2008.07.007. |
| [56] | Starr T, Child R, Wehrly T D, et al. Selective Subversion of Autophagy Complexes Facilitates Completion of the Brucella Intracellular Cycle[J]. Cell Host Microbe, 2012, 11(1): 33-45. doi:10.1016/j.chom.2011.12.002. |
| [57] | Kambarev S, Borghesan E, Miller C N, et al. The Brucella abortus Type IV Effector BspA Inhibits MARCH6-Dependent ERAD To Promote Intracellular Growth[J]. Infect Immun, 2023, 91(5): e0013023. doi:10.1128/iai.00130-23. |
| [58] | Spera J M, Guaimas F, Czibener C, et al. Brucella Egresses from Host Cells Exploiting Multivesicular Bodies[J]. Mbio, 2023, 14(1): e0333822. doi:10.1128/mbio.03338-22. |
| [59] | Qin Y Q, Zhou G X, Jiao F Y, et al. Brucella mediates autophagy, inflammation, and apoptosis to escape host killing[J]. Front Cell Infect Microbiol, 2024, 14: 1408407. doi:10.3389/fcimb.2024.1408407. |
| [60] | 龚思露, 邹燕. 非编码RNA在沙眼衣原体感染中的作用[J]. 中国人兽共患病学报, 2024, 40(3): 257-263. doi:10.3969/j.issn.1002-2694.2024.00.040. |
| [61] |
Panis G, Murray S R, Viollier P H. Versatility of global transcriptional regulators in alpha-Proteobacteria: from essential cell cycle control to ancillary functions[J]. FEMS Microbiol Rev, 2015, 39(1): 120-133. doi:10.1093/femsre/fuu002.
pmid: 25793963 |
| [62] | Campbell M, Barton I S, Roop R M, et al. Comparison of CcrM-dependent methylation in Caulobacter crescentus and Brucella abortus by nanopore sequencing[J]. J Bacteriol, 2024, 206(6): e0008324. doi:10.1128/jb.00083-24. |
| [63] | Reich N O, Dang E, Kurnik M, et al. The highly specific, cell cycle-regulated methyltransferase from Caulobacter crescentus relies on a novel DNA recognition mechanism[J]. J Biol Chem, 2018, 293(49): 19038-19046. doi:10.1074/jbc.RA118.005212. |
| [64] | Deng X M, Guo J, Sun Z H, et al. Brucella-Induced Downregulation of lncRNA Gm28309 Triggers Macrophages Inflammatory Response Through the miR-3068-5p/NF-κB Pathway[J]. Front Immunol, 2020, 11:581517. doi:10.3389/fimmu.2020.581517. |
| [65] | Jiao H W, Nie X, Zhu H P, et al. miR-146b-5p Plays a Critical Role in the Regulation of Autophagy in increment per Brucella melitensis-Infected RAW264.7 Cells[J]. Biomed Res Int, 2020: 1953242. doi:10.1155/2020/1953242. |
| [66] | Corsetti P P, de Almeida L A, Gonçalves A N A, et al. miR-181a-5p Regulates TnF-α and miRr-21a-5p Influences Gualynate-Binding Protein 5 and IL-10 Expression in Macrophages Affecting Host Control of Brucella abortus Infection[J]. Front Immunol, 2018, 9: 1331. doi:10.3389/fimmu.2018.01331. |
| [67] | Xu D, Song J B, Li G W, et al. A novel small RNA Bmsr1 enhances virulence in Brucella melitensis M28[J]. Vet Microbiol, 2018, 223: 1-8. doi:10.1016/j.vetmic.2018.07.007. |
| [68] | 马冬冰, 王亮. miR-133a在骨质疏松性骨折的表达及成骨细胞活性的调控作用[J]. 中国骨质疏松杂志, 2026, 32(5):683-690,696. doi:10.3969/j.issn.1006-7108.2026.05.009. |
| [69] | 季诗煜, 李莎, 高润清, 等. miRNA调控NLRP3炎症小体靶向滑膜细胞焦亡在类风湿关节炎骨破坏中的治疗前景[J/OL]. 细胞与分子免疫学杂志, 1-12[2026-01-14]. https://doi.org/10.13423/j.cnki.cjcmi.010083. |
| [70] |
Matsushita Y, Nagata M, Kozloff K M, et al. A Wnt-mediated transformation of the bone marrow stromal cell identity orchestrates skeletal regeneration[J]. Nat Commun, 2020, 11(1): 332. doi:10.1038/s41467-019-14029-w.
pmid: 31949165 |
| [71] | Zhuang X M, Zhou B, Yuan K F. Role of p53 mediated miR-23a/CXCL12 pathway in osteogenic differentiation of bone mesenchymal stem cells on nanostructured titanium surfaces[J]. Biomed Pharmacother, 2019, 112: 108649. doi:10.1016/j.biopha.2019.108649. |
| [72] | Wang S, Xia D, Dou W, et al. Bioactive Porous Composite Implant Guides Mesenchymal Stem Cell Differentiation and Migration to Accelerate Bone Reconstruction[J]. Int J Nanomedicine, 2024, 19:12111-12127. doi:10.2147/IJN.S479893. |
| [73] |
Schajnovitz A, Itkin T, D’Uva G, et al. CXCL12 secretion by bone marrow stromal cells is dependent on cell contact and mediated by connexin-43 and connexin-45 gap junctions[J]. Nat Immunol, 2011, 12(5): 391-398. doi:10.1038/ni.2017.
pmid: 21441933 |
| [74] | Chen J L, Zhi F J, Zhao G H, et al. Brucella osteoarthritis: recent progress and future directions[J]. Front Microbiol, 2025, 16: 1522537. doi:10.3389/fmicb.2025.1522537. |
| [75] | Jiang S, Li H, Zhang L, et al. Generic Diagramming Platform (GDP): a comprehensive database of high-quality biomedical graphics[J]. Nucleic Acids Res, 2025, 53(D1): D1670-D1676. doi:10.1093/nar/gkae973. |
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