The current state of animal models and genomic approaches towards identifying and validating molecular determinants of Mycobacterium tuberculosis infection and tuberculosis disease

被引:30
作者
Bucsan, Allison N. [1 ,2 ,6 ]
Mehra, Smriti [2 ]
Khader, Shabaana A. [3 ]
Kaushal, Deepak [1 ,2 ,4 ,5 ]
机构
[1] Tulane Ctr TB Res, Covington, LA USA
[2] Tulane Natl Primate Res Ctr, Covington, LA USA
[3] Washington Univ St Louis, St Louis, MO USA
[4] Southwest Natl Primate Res Ctr, San Antonio, TX USA
[5] Texas Biomed Res Inst, San Antonio, TX USA
[6] Uniformed Serv Univ Hlth Sci, Malaria Lab, Bethesda, MD 20814 USA
来源
PATHOGENS AND DISEASE | 2019年 / 77卷 / 04期
关键词
Mycobacterium tuberculosis; animal models; translation; T-CELL RESPONSES; NONHUMAN PRIMATE MODEL; RABBIT MODEL; GRANULOMA-FORMATION; MACAQUE MODEL; SIGMA-FACTOR; PULMONARY TUBERCULOSIS; GUINEA-PIG; CYNOMOLGUS MACAQUES; PROTECTIVE IMMUNITY;
D O I
10.1093/femspd/ftz037
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Animal models are important in understanding both the pathogenesis of and immunity to tuberculosis (TB). Unfortunately, we are beginning to understand that no animal model perfectly recapitulates the human TB syndrome, which encompasses numerous different stages. Furthermore, Mycobacterium tuberculosis infection is a very heterogeneous event at both the levels of pathogenesis and immunity. This review seeks to establish the current understanding of TB pathogenesis and immunity, as validated in the animal models of TB in active use today. We especially focus on the use of modern genomic approaches in these models to determine the mechanism and the role of specific molecular pathways. Animal models have significantly enhanced our understanding of TB. Incorporation of contemporary technologies such as single cell transcriptomics, high-parameter flow cytometric immune profiling, proteomics, proteomic flow cytometry and immunocytometry into the animal models in use will further enhance our understanding of TB and facilitate the development of treatment and vaccination strategies.
引用
收藏
页数:17
相关论文
共 233 条
  • [1] [Anonymous], 2000, MMWR Recomm Rep, V49, P1
  • [2] Rationalized design of a mucosal vaccine protects against Mycobacterium tuberculosis challenge in mice
    Ahmed, Mushtaq
    Jiao, Hongmei
    Domingo-Gonzalez, Racquel
    Das, Shibali
    Griffiths, Kristin L.
    Rangel-Moreno, Javier
    Nagarajan, Uma M.
    Khader, Shabaana A.
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 2017, 101 (06) : 1373 - 1381
  • [3] Updates on the risk factors for latent tuberculosis reactivation and their managements
    Ai, Jing-Wen
    Ruan, Qiao-Ling
    Liu, Qi-Hui
    Zhang, Wen-Hong
    [J]. EMERGING MICROBES & INFECTIONS, 2016, 5
  • [4] ANACKER RL, 1972, Z IMMUNITATSFORSCH, V143, P363
  • [5] Allelic exchange in Mycobacterium tuberculosis with long linear recombination substrates
    Balasubramanian, V
    Pavelka, MS
    Bardarov, SS
    Martin, J
    Weisbrod, TR
    McAdam, RA
    Bloom, BR
    Jacobs, WR
    [J]. JOURNAL OF BACTERIOLOGY, 1996, 178 (01) : 273 - 279
  • [6] BARCLAY W R, 1970, Infection and Immunity, V2, P574
  • [7] BARCLAY WR, 1973, AM REV RESPIR DIS, V107, P351
  • [8] Interleukin-10 promotes Mycobacterium tuberculosis disease progression in CBA/J mice
    Beamer, Gillian L.
    Flaherty, David K.
    Assogba, Barnabe D.
    Stromberg, Paul
    Gonzalez-Juarrero, Mercedes
    Malefyt, Rene de Waal
    Vesosky, Bridget
    Turner, Joanne
    [J]. JOURNAL OF IMMUNOLOGY, 2008, 181 (08) : 5545 - 5550
  • [9] A historical and molecular phylogeny of BCG strains
    Behr, MA
    Small, PM
    [J]. VACCINE, 1999, 17 (7-8) : 915 - 922
  • [10] Has BCG attenuated to impotence?
    Behr, MA
    Small, PM
    [J]. NATURE, 1997, 389 (6647) : 133 - 134