Altered inflammatory responses following transforming growth factor-β neutralization in experimental guinea pig tuberculous pleurisy

被引:20
作者
Allen, Shannon Sedberry
Mackie, John T. [2 ]
Russell, Karen [2 ]
Jeevan, Amminikutty
Skwor, Troy A.
McMurray, David N. [1 ]
机构
[1] Texas A&M Univ, Syst Hlth Sci Ctr, Coll Med, Dept Microbiol & Mol Pathogenesis, College Stn, TX 77843 USA
[2] Texas A&M Univ, Coll Vet Med, Dept Pathobiol, College Stn, TX 77843 USA
基金
美国国家卫生研究院;
关键词
tuberculosis; guinea pig; pleuritis; TGF-beta;
D O I
10.1016/j.tube.2008.05.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The predominant extrapulmonary form of tuberculosis, which develops in 10% of diseased individuals, is pleurisy. The immune response mounted against Mycobacterium tuberculosis in the pleural cavity is one that is sufficient for clearing the organism without therapeutic intervention. Thus, examining the role of immune constituents in this context will provide understanding of the vital role they play in controlling tuberculosis. In this study, experimental tuberculous pleurisy was induced in guinea pigs, and anti-TGF-beta was administered intrapleurally to the guinea pigs daily throughout the study (8 days). Neutralizing TGF-beta resulted in a significant reduction in the percentage of lymphocytes and CD8(+) cells present in the pleural. exudate, decreased proliferative responses of pleural cells to ConA and PPD, and decreased mRNA expression of IFN-gamma and CCL5 in pleural. effusion cells. Conversely, the percentage of neutrophils was significantly increased in anti-TGF-beta-treated guinea pigs, along with upregulated mRNA expression of CXCL8. The percentage of macrophages in the pleural exudate, TNF-alpha and IL-12p40 mRNA expression, and the histopathotogical. response were not significantly altered. While TGF-beta is generally thought of as an immunosuppressive cytokine, the results of this study demonstrate its importance in promoting an inflammatory response, and highlight its bipolar nature. (c) 2008 Elsevier Ltd. All. rights reserved.
引用
收藏
页码:430 / 436
页数:7
相关论文
共 37 条
  • [21] MAEDA J, 1993, CLIN EXP IMMUNOL, V92, P32
  • [22] Bacterial meningitis: The role of transforming growth factor-beta in innate immunity and secondary brain damage
    Malipiero, Ursula
    Koedel, Uwe
    Pfister, Walter
    Fontana, Adriano
    [J]. NEURODEGENERATIVE DISEASES, 2007, 4 (01) : 43 - 50
  • [23] TRANSFORMING GROWTH-FACTOR-BETA - A MATTER OF LIFE AND DEATH
    MCCARTNEYFRANCIS, NL
    WAHL, SM
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1994, 55 (03) : 401 - 409
  • [24] Circulating TNF-α, TGF-β, and IL-10 in tuberculosis patients and healthy contacts
    Olobo, JO
    Geletu, M
    Demissie, A
    Eguale, T
    Hiwot, K
    Aderaye, G
    Britton, S
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2001, 53 (01) : 85 - 91
  • [25] PAREKH T, 1994, J IMMUNOL, V152, P2456
  • [26] LYMPHOCYTE-T RESPONSE IN A GUINEA-PIG MODEL OF TUBERCULOUS PLEURITIS
    PHALEN, SW
    MCMURRAY, DN
    [J]. INFECTION AND IMMUNITY, 1993, 61 (01) : 142 - 145
  • [27] ROPER WH, 1955, AM REV TUBERC PULM, V71, P616
  • [28] BCG vaccination of guinea pigs modulates Mycobacterium tuberculosis-induced CCL5 (RANTES) production in vitro and in vivo
    Skwor, Troy A.
    Allen, Shannon Sedberry
    Mackie, John T.
    Russell, Karen
    Berghman, Luc R.
    McMurray, David N.
    [J]. TUBERCULOSIS, 2006, 86 (06) : 419 - 429
  • [29] Smith WB, 1996, J IMMUNOL, V157, P360
  • [30] SPACCAPELO R, 1995, J IMMUNOL, V155, P1349