Literature DB >> 1544223

Induction and expression of protective T cells during Mycobacterium avium infections in mice.

R Appelberg1, J Pedrosa.   

Abstract

Mycobacterium avium is an opportunistic pathogen that infects individuals suffering from chronic lung disease or immunocompromised patients such as AIDS patients. Here we show that a highly virulent isolate of M. avium proliferated as extensively in T cell deficient as in immunocompetent mice. T cell deficient mice allowed a progressive growth of a less virulent AIDS-derived isolate of M. avium while immunocompetent mice arrested the growth of this isolate. Adoptive transfer of T cell enriched spleen cells between congenic strains of mice differing at the Bcg/Ity/Lsh locus showed that only naturally resistant BALB/c.Bcgr (C.D2) mice infected with the highly virulent strain of M. avium or the naturally susceptible BALB/c mice infected with the lower virulence isolate developed protective T cells and that these cells only mediated protection when transferred to naturally susceptible, but not to naturally resistant, mice. Both strains of M. avium proliferated in bone marrow-derived macrophages cultured in vitro and they were both susceptible to the bacteriostatic effects induced in the macrophages by crude lymphokines produced by concanavalin A-stimulated spleen cells.

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Year:  1992        PMID: 1544223      PMCID: PMC1554342          DOI: 10.1111/j.1365-2249.1992.tb03006.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  36 in total

1.  Stimulation of a major subset of lymphocytes expressing T cell receptor gamma delta by an antigen derived from Mycobacterium tuberculosis.

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2.  Regulation of host resistance to Mycobacterium intracellulare in vivo and in vitro by the Bcg gene.

Authors:  Y Goto; E Buschman; E Skamene
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3.  The role of macrophage activation and of Bcg-encoded macrophage function(s) in the control of Mycobacterium avium infection in mice.

Authors:  R Appelberg; A M Sarmento
Journal:  Clin Exp Immunol       Date:  1990-06       Impact factor: 4.330

Review 4.  Nontuberculous mycobacteria and associated diseases.

Authors:  E Wolinsky
Journal:  Am Rev Respir Dis       Date:  1979-01

5.  Growth of mycobacterium bovis (BCG) in T lymphocyte-depleted mice.

Authors:  F M Collins; C C Congdon; N E Morrison
Journal:  Infect Immun       Date:  1975-01       Impact factor: 3.441

6.  Lymphocytes bearing antigen-specific gamma delta T-cell receptors accumulate in human infectious disease lesions.

Authors:  R L Modlin; C Pirmez; F M Hofman; V Torigian; K Uyemura; T H Rea; B R Bloom; M B Brenner
Journal:  Nature       Date:  1989-06-15       Impact factor: 49.962

7.  Killing of Mycobacterium smegmatis by macrophages from genetically susceptible and resistant mice.

Authors:  M Denis; A Forget; M Pelletier; F Gervais; E Skamene
Journal:  J Leukoc Biol       Date:  1990-01       Impact factor: 4.962

8.  T-cell-mediated protection of mice against virulent Mycobacterium tuberculosis.

Authors:  C Leveton; S Barnass; B Champion; S Lucas; B De Souza; M Nicol; D Banerjee; G Rook
Journal:  Infect Immun       Date:  1989-02       Impact factor: 3.441

9.  Induction of non-specific immunosuppression in mice by mycobacterial infections and its relationship to macrophage activation.

Authors:  R Appelberg; R Soares; P Ferreira; M T Silva
Journal:  Scand J Immunol       Date:  1989-08       Impact factor: 3.487

10.  Properties of purified T cell subsets. I. In vitro responses to class I vs. class II H-2 alloantigens.

Authors:  J Sprent; M Schaefer
Journal:  J Exp Med       Date:  1985-12-01       Impact factor: 14.307

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  13 in total

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Authors:  M A Holsti; J S Schorey; E J Brown; P M Allen
Journal:  Infect Immun       Date:  1998-03       Impact factor: 3.441

2.  Processing and presentation of an antigen of Mycobacterium avium require access to an acidified compartment with active proteases.

Authors:  M A Holsti; P M Allen
Journal:  Infect Immun       Date:  1996-10       Impact factor: 3.441

Review 3.  Pathogenesis of Mycobacterium avium infection: typical responses to an atypical mycobacterium?

Authors:  Rui Appelberg
Journal:  Immunol Res       Date:  2006       Impact factor: 2.829

4.  T-cell-independent granuloma formation in response to Mycobacterium avium: role of tumour necrosis factor-alpha and interferon-gamma.

Authors:  D Smith; H Hänsch; G Bancroft; S Ehlers
Journal:  Immunology       Date:  1997-12       Impact factor: 7.397

5.  Protection against virulent Mycobacterium avium infection following DNA vaccination with the 35-kilodalton antigen is accompanied by induction of gamma interferon-secreting CD4(+) T cells.

Authors:  E Martin; A T Kamath; J A Triccas; W J Britton
Journal:  Infect Immun       Date:  2000-06       Impact factor: 3.441

6.  Tumour necrosis factor-alpha (TNF-alpha) in the host resistance to mycobacteria of distinct virulence.

Authors:  R Appelberg; A Sarmento; A G Castro
Journal:  Clin Exp Immunol       Date:  1995-08       Impact factor: 4.330

7.  Susceptibility of beige mice to Mycobacterium avium: role of neutrophils.

Authors:  R Appelberg; A G Castro; S Gomes; J Pedrosa; M T Silva
Journal:  Infect Immun       Date:  1995-09       Impact factor: 3.441

8.  The relative impact of bacterial virulence and host genetic background on cytokine expression during Mycobacterium avium infection of mice.

Authors:  A G Castro; P Minóprio; R Appelberg
Journal:  Immunology       Date:  1995-08       Impact factor: 7.397

9.  Host response to nontuberculous mycobacterial infections of current clinical importance.

Authors:  Ian M Orme; Diane J Ordway
Journal:  Infect Immun       Date:  2014-06-09       Impact factor: 3.441

10.  Role of interleukin-6 in the induction of protective T cells during mycobacterial infections in mice.

Authors:  R Appelberg; A G Castro; J Pedrosa; P Minóprio
Journal:  Immunology       Date:  1994-07       Impact factor: 7.397

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