Stealth Strategies of Mycobacterium tuberculosis for Immune Evasion

被引:10
|
作者
Naeem, Muhammad Ahsan [1 ]
Ahmad, Waqas [1 ]
Tyagi, Rohit [2 ]
Akram, Qaiser [1 ]
Younus, Muhammad [1 ]
Liu, Xilin [3 ]
机构
[1] Univ Coll Vet & Anim Sci, Narowal 51600, Pakistan
[2] Huazhong Agr Univ, Coll Vet Med, Wuhan 430070, Peoples R China
[3] Jilin Univ, China Japan Union Hosp, Dept Hand Surg, 126 XianTai St, Changchun, Peoples R China
关键词
T-CELL; INTRACELLULAR SURVIVAL; GRANULOMA-FORMATION; CRYSTAL-STRUCTURE; IRON ACQUISITION; OXIDATIVE STRESS; M; TUBERCULOSIS; KEY ENZYME; PROTEIN; MACROPHAGES;
D O I
10.21775/cimb.041.597
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tuberculosis is a devastating disease causing high mortality all over the world, especially in the developing countries. Mycobacterium tuberculosis (M. tb) is the causative agent of tuberculosis which replicates in the intracellular environment of host macrophages. Although the host immune system is capable of completely eliminating the pathogen, co-evolution of M. tb with humans has resulted in its ability to hijack the host innate and adaptive immune systems in numerous ways. Limited recent progress has been made in the understanding of M. tb immune escape mechanisms, hence exploration of survival strategies of M. tb has been critically reviewed with an insight into understanding its pathogenesis. We summarized the recent studies regarding the modulation of innate immune response, adaptive immune response, epigenetics and the role of miRNA. All of these advancements suggest that M. tb is well-familiarize with the host immune system and possess the ability to hijack it for intracellular survival.
引用
收藏
页码:597 / 616
页数:20
相关论文
共 50 条
  • [11] Outcome of Mycobacterium tuberculosis and Toll-like receptor interaction: immune response or immune evasion?
    Saraav, Iti
    Singh, Swati
    Sharma, Sadhna
    IMMUNOLOGY AND CELL BIOLOGY, 2014, 92 (09): : 741 - 746
  • [12] TREM2 Promotes Immune Evasion by Mycobacterium tuberculosis in Human Macrophages
    Dabla, Ankita
    Liang, Yi Chu
    Rajabalee, Nusrah
    Irwin, Courtney
    Moonen, Carolyn G. J.
    Willis, Jessie, V
    Berton, Stefania
    Sun, Jim
    MBIO, 2022, 13 (04):
  • [13] MPT64 polymorphisms of Mycobacterium tuberculosis strains suggest ongoing immune evasion
    Jiang, Yi
    Liu, Haican
    Wan, Kanglin
    TUBERCULOSIS, 2014, 94 (06) : 712 - 714
  • [14] Host Evasion and Exploitation Schemes of Mycobacterium tuberculosis
    Cambier, C. J.
    Falkow, Stanley
    Ramakrishnan, Lalita
    CELL, 2014, 159 (07) : 1497 - 1509
  • [15] Evasion and subversion of antigen presentation by Mycobacterium tuberculosis
    Baena, A.
    Porcelli, S. A.
    TISSUE ANTIGENS, 2009, 74 (03): : 189 - 204
  • [16] Evasion of Innate and Adaptive Immunity by Mycobacterium tuberculosis
    Goldberg, Michael F.
    Saini, Neeraj K.
    Porcelli, Steven A.
    MICROBIOLOGY SPECTRUM, 2014, 2 (05):
  • [17] Strategies of tumor immune evasion
    Seliger, B
    BIODRUGS, 2005, 19 (06) : 347 - 354
  • [18] Viral strategies of immune evasion
    Ploegh, HL
    SCIENCE, 1998, 280 (5361) : 248 - 253
  • [19] Lymphoma: Immune Evasion Strategies
    Upadhyay, Ranjan
    Hammerich, Linda
    Peng, Paul
    Brown, Brian
    Merad, Miriam
    Brody, Joshua D.
    CANCERS, 2015, 7 (02) : 736 - 762
  • [20] Immune Evasion Strategies of Glioblastoma
    Razavi, Seyed-Mostafa
    Lee, Karen E.
    Jin, Benjamin E.
    Aujla, Parvir S.
    Gholamin, Sharareh
    Li, Gordon
    FRONTIERS IN SURGERY, 2016, 3