Literature DB >> 7682995

The mycobacterial secreted antigen 85 complex possesses epitopes that are differentially expressed in human leprosy lesions and Mycobacterium leprae-infected armadillo tissues.

A Rambukkana1, J D Burggraaf, W R Faber, M Harboe, P Teeling, S Krieg, P K Das.   

Abstract

The granulomatous skin lesions in leprosy are thought to be initiated by the immune response to certain antigens of the causative agent, Mycobacterium leprae. The antigen 85 complex is one of the major targets in the immune response to M. leprae infection. In the present study, a panel of previously characterized monoclonal antibodies (MAbs) (3A8, Rb2, A4g4, A2h11, Pe12, and A3c12) reacting with different epitopes of the 85 complex proteins of Mycobacterium tuberculosis and M. leprae was employed in a comparative immunohistological analysis to demonstrate the in situ expression of 85 complex antigenic epitopes in leprosy lesions across the clinical spectrum and in M. leprae-infected armadillo liver tissues. These MAbs showed a heterogeneous staining pattern in a given leprosy lesion. In highly bacilliferous borderline and lepromatous leprosy lesions, MAbs Rb2, A4g4, A2h11, and Pe12 stained clear rod-shaped M. leprae bacilli within macrophages, and the degree of staining correlated with the bacillary index of the lesion. On the other hand, MAbs 3A8 and A3c12 staining was mostly seen as a diffuse staining pattern within interstitial spaces and on the membranes of the infiltrated cells but not the bacilli. In paucibacillary borderline and tuberculoid leprosy lesions, only 3A8, Rb2, and A3c12 showed distinct staining in association with infiltrates in the granuloma. None of these MAbs showed any detectable reaction with control nonleprosy skin lesions, while MAb A3c12 positively stained the granulomas of both leprosy and control specimens. In situ reactivity of these MAbs with M. leprae-infected armadillo liver tissues also showed a heterogeneous staining pattern. Interestingly, a clear difference in expression of these epitopes was observed between armadillo tissues and human leprosy lesions. By immunogold ultracytochemistry, we further showed the differential localization of these MAb-reactive epitopes on the cell surface, in the cytosol, and at the vicinity of M. leprae within Kupffer cells of armadillo liver tissues. Our results indicate that these antigenic epitopes of the antigen 85 complex are differentially expressed in leprosy lesions and infected armadillo tissues and that they could be target determinants in the immunopathological responses during M. leprae infection.

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Year:  1993        PMID: 7682995      PMCID: PMC280773          DOI: 10.1128/iai.61.5.1835-1845.1993

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  31 in total

1.  Immune responsiveness to Mycobacterium leprae and other mycobacterial antigens throughout the clinical and histopathological spectrum of leprosy.

Authors:  B Myrvang; T Godal; D S Ridley; S S Fröland; Y K Song
Journal:  Clin Exp Immunol       Date:  1973-08       Impact factor: 4.330

2.  The pathogenesis of the early skin lesion in leprosy.

Authors:  D S Ridley
Journal:  J Pathol       Date:  1973-11       Impact factor: 7.996

3.  MPB59, a widely cross-reacting protein of Mycobacterium bovis BCG.

Authors:  H G Wiker; M Harboe; S Nagai; M E Patarroyo; C Ramirez; N Cruz
Journal:  Int Arch Allergy Appl Immunol       Date:  1986

4.  Classification of leprosy according to immunity. A five-group system.

Authors:  D S Ridley; W H Jopling
Journal:  Int J Lepr Other Mycobact Dis       Date:  1966 Jul-Sep

5.  Demonstration of mycobacterial antigens in leprosy tissues.

Authors:  R N Mshana; A Belehu; G L Stoner; M Harboe; A Haregewoin
Journal:  Int J Lepr Other Mycobact Dis       Date:  1982-03

6.  Demonstration of mycobacterial antigens in nerve biopsies from leprosy patients using peroxidase-antiperoxidase immunoenzyme technique.

Authors:  R N Mshana; D P Humber; M Harboe; A Belehu
Journal:  Clin Immunol Immunopathol       Date:  1983-12

7.  Demonstration of Mycobacterium leprae specific antigens in leprosy lesions using monoclonal antibodies.

Authors:  R B Narayanan; G Ramu; S Sinha; U Sengupta; G N Malaviya; K V Desikan
Journal:  Indian J Lepr       Date:  1985 Apr-Jun

8.  Heterogeneity of monoclonal antibody-reactive epitopes on mycobacterial 30-kilodalton-region proteins and the secreted antigen 85 complex and demonstration of antigen 85B on the Mycobacterium leprae cell wall surface.

Authors:  A Rambukkana; P K Das; J D Burggraaf; S Yong; W R Faber; J E Thole; M Harboe
Journal:  Infect Immun       Date:  1992-12       Impact factor: 3.441

9.  Learning from lesions: patterns of tissue inflammation in leprosy.

Authors:  R L Modlin; J Melancon-Kaplan; S M Young; C Pirmez; H Kino; J Convit; T H Rea; B R Bloom
Journal:  Proc Natl Acad Sci U S A       Date:  1988-02       Impact factor: 11.205

10.  The cutaneous infiltrates of leprosy: cellular characteristics and the predominant T-cell phenotypes.

Authors:  W C Van Voorhis; G Kaplan; E N Sarno; M A Horwitz; R M Steinman; W R Levis; N Nogueira; L S Hair; C R Gattass; B A Arrick; Z A Cohn
Journal:  N Engl J Med       Date:  1982-12-23       Impact factor: 91.245

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  4 in total

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Journal:  Clin Exp Immunol       Date:  1995-01       Impact factor: 4.330

2.  The Mycobacterium bovis 32-kilodalton protein antigen induces human cytotoxic T-cell responses.

Authors:  M E Munk; J De Bruyn; H Gras; S H Kaufmann
Journal:  Infect Immun       Date:  1994-02       Impact factor: 3.441

3.  The domains of human fibronectin mediating the binding of alpha antigen, the most immunopotent antigen of mycobacteria that induces protective immunity against mycobacterial infection.

Authors:  M Naito; T Fukuda; K Sekiguchi; T Yamada
Journal:  Biochem J       Date:  2000-05-01       Impact factor: 3.857

4.  Inflammatory responses to infection: the Dutch contribution.

Authors:  Martijn A Nolte; Jos W M van der Meer
Journal:  Immunol Lett       Date:  2014-10-18       Impact factor: 3.685

  4 in total

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