Progression of chronic pulmonary tuberculosis in mice aerogenically infected with virulent Mycobacterium tuberculosis

Tubercle and Lung Disease

Volumn 78, Issue 1, 1997, Pages 57-66

  Rhoades, E R ^a  

^a Veterinary Dentistry and Oral Surgery   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AEROSOL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BACTERIAL COUNT; BACTERIAL VIRULENCE; CELL TYPE; CELLULAR DISTRIBUTION; CONTROLLED STUDY; DEATH; DISEASE COURSE; DISEASE SEVERITY; FIBROSING ALVEOLITIS; FOLLOW UP; GRANULOMATOSIS; GUINEA PIG; HOST; IMMUNE RESPONSE; LUNG INJURY; LUNG TUBERCULOSIS; LYMPHOCYTE; MOUSE; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; RABBIT; RESPIRATORY EPITHELIUM; RESPIRATORY TRACT DISEASE; SPECIES DIFFERENCE; STAGING; STRAIN DIFFERENCE; TISSUE NECROSIS;

EID: 0031442875     PISSN: 09628479     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0962-8479(97)90016-2     Document Type: Article

References (39)

1. Orme I M, Andersen P, Boom W H. T cell response to Mycobacterium tuberailosis. J lnfect. Dis 1993; 167:1481-1497.
2. Cooper A M. The protective immune response to Mycobacterium tuberculosis. Curr Opin Immunol 1995; 7:512-516.
3. Orme I M. A mouse model of the recrudescence of latent tuberculosis in the elderly. Am Rev Respir Dis 1988; 137:716-718.
4. Epstein W L Granulomatous hypersensitivity. Prog Allergy 1967; 11: 36-88.
5. North R J. The relative importance of blood monocytes and fixed macrophages to the expression of cell-mediated immunity to infection. J Exp Med 1970; 132:521-532.
6. Dunn P L, North R J. Virulence ranking of some Mycobacterium tuberculosis and Mycobacterium bovis strains according to their ability to multiply in the lungs, induce lung pathology, and cause mortality in mice. Infect Immun 1995; 63:3428-3437.
7. Nibbering P H, Van Der Hiede G A, Van Furth R. Immunohistochemical analysis of cellular responses to BCG. Clin Exp Immunol 1989; 75:147-154.
8. Orrell J M, Brett S J, Ivanyi J, Coghill G, Grant A, Beck J S. Measurement of the tissue distribution of immunoperoxidase staining with polyclonal anti-BCG serum in lung granulomata of mice infected with Mycobacterium tuberculosis. J Pathol 1991; 164:41-45.
9. Orrell J M, Brett S J, Ivanyi J, Coghill G, Grant A, BeckJ S. Morphometric analysis of Mycobacterium tuberculosis infection in mice suggests a genetic influence on the generation of the granulomatous inflammatory response. J Pathol 1992; 166:77-82.
10. Rich A R. The pathogenesis of tuberculosis. Springfield: Charles C. Thomas, 1951.
11. Smith D W, McMurray D N, VViegeshaus E H, Grover A A, Harding G E. Host-parasite relationships in experimental airborne tuberculosis. IV. Early events in the course of infection in vaccinated and nonvaccinated guinea pigs. Am Rev Respir Dis 1970; 102:937-949.
12. Smith D W, Harding G E. Animal model of human disease. Animal model: experimental airborne tuberculosis in the guinea pig. Am J Pathol 1977; 89:273-276.
13. Converse P J, Dannenberg A M, Jr Estep J E et al. Cavitary tuberculosis produced in rabbits by aerosolized virulent tubercle bacilli. Infect Immun 1996; 64:4776-4787.
14. Medlar E M. The behaviour of pulmonary tuberculous lesions. Am Rev Tuber Pul Dis 1955; 71:1-244.
15. Dannenberg A M Jr, Ando M, Shima K. Macrophage accumulation, division maturation, and digestive and microbicidal capacities in tuberculous lesions. HI. The turnover of macrophages and its relation to their activation and antimicrobial immunity in primary BCG lesions and those of reinfection. J Immunol 1972; 109:1109-1121.
16. Ordway D J, Sonnenberg M G, Donahue S A, Belisle J T, Orme I M. Drug-resistant strains of Mycobacterium tuberculosis exhibit a wide range of virulence for mice. Infect Immun 1995; 63:741-743.
17. Rhoades E R, Cooper A M, Orme I M. Chemokine response in mice infected with Mycobacterium tuberculosis. Infect Immun 1995; 63:3871-3877.
18. Jones T C, Hunt R D. Veterinary pathology. Philadelphia: Lea & Febiger, 1983:26-27.
19. North R J. Mycobacterium tuberculosis is strikingly more virulent for mice when given via the respiratory than via the intravenous route. J Infect Dis 1995; 172:1550-1553.
20. Brett S, Orrell J M, Swanson Beck J, Ivanyi J. Influence of H-2 genes on growth of Mycobacterium tuberculosis in the lungs of chronically infected mice. Immunology 1992; 76:129-132.
21. Medina E, North R J. Evidence inconsistent with a role for the Beg gene (Nrampl) in resistance of mice to infection with virulent Mycobacterium tuberculosis.] Exp Med 1996; 183:1045-1051.
22. Collins F M, Congdon C C, Morrison N E. Growth of Mycobacterium bovis (BCG) in T lymphocyte-depleted mice. Infect Immun 1975; 11:57-64.
23. Adams D O. The biology of the granuloma. In: loachim H L, ed. Pathology of granulomas. New York: Raven Press, 1983:1-20.
24. Dannenberg A M Jr. Immunopathogenesis of pulmonary tuberculosis. Hosp Pract (Off Ed) 1993; 28:51-58.
25. McMurray D N. Guinea pig model of tuberculosis. In: Bloom B R, ed. Tuberculosis: pathogenesis, protection and control. Washington DC: ASM Press. 1994:135-147.
26. Dannenberg A M Jr. Rabbit model of tuberculosis. In: Bloom B R, ed. Tuberculosis: pathogenesis, protection, and control. Washington, DC: ASM Press, 1994:149-156.
27. Appelberg R Macrophage inflammatory proteins MIP-1 and MIP-2 are involved in T cell-mediated neutrophil recruitment. J Leukoc Biol 1992; 52:303-306.
28. Austrup F, Vestweber D, Borges E et al. P- and E-selectin mediate recruitment of T-helper-1 but not T-heIper-2 cells into inflamed tissues. Nature 1997; 385:81-84.
29. Borges E, Tietz W, Steegmaier M et al. P-selectin glycoprotein Iigand-1 (PSGL-1) on T helper I but not T helper 2 cells binds to P-selectin and supports migration into inflamed skin. J Exp Med 1997; 185:573-579.
30. Dünn P L, North R J. Persistent infection with virulent but not avirulent Mycobacterium tuberculosis in the lungs of mice causes progressive pathology. J Med Microbiol 1996; 45:103-109.
31. Chatterjee D, Roberts A D, Lowell K, Brennan P J, Orme I M. Structural basis of capacity of lipoarabinomannan to induce secretion of tumor necrosis factor. Infect Immun 1992; 60:1249-1253.
32. Roach TI A, Barton C H, Chatterjee D, Blackwell J M. Macrophage activation: lipoarabinomannan from avirulent and virulent strains of Mycobacterium tuberculosis differentially induces the early genes c-fos, KC, JE, and tumor necrosis factor-ajlmmunol 1993; 150:1886-1896.
33. Orme I M. Aging and immunity to tuberculosis: increased susceptibility of old mice reflects a decreased capacity to generate mediator T lymphocytes. J Immunol 1987; 138:4414-4418.
34. Orme I M, Griffin J P, Roberts A D, Ernst D N. Evidence for a defective accumulation of protective T cells in old mice infected with Mycobacterium tuberculosis. Cell Immunol 1993; 147:222-226.
35. Cooper A M, Callahan J E, Griffin J P, Roberts A D, Orme I M. Old mice are able to control low-dose aerogenic infections with Mycobacterium tuberculosis. Infect Immun 1995; 63:3259-3265.
36. Cooper A M, Roberts A D, Rhoades E R, Callahan J E, Getzy D M, Orme I M. The role of interleukin-12 in acquired immunity to Mycobacterium titbemtlosis infection. Immunology 1995; 84:423-432.
37. Fiorentino D F, Bond M A, Mosmann T R. Two types of mouse helper T cells IV. Th2 clones secrete a factor that inhibits cytokine production by Thl clones. J Exp Med 1989; 170:2081-2088.
38. Li L, Elliot J F, Mossman T R. IL-10 inhibits cytokine production, vascular leakage and swelling during Th-1-induced delayed-type hypersensitivty. J Immunol 1994; 153:3967-3978.
39. Bermudez L E. Production of transforming growth factor-β by Mycobacterium rtn'HwHnfected human macrophages is associated with unresponsiveness to IFN-y.J Immunol 1993; 150:1838-1845.