Literature DB >> 7713549

Immunohistochemical analysis of cell composition and in situ cytokine expression in HIV- and non-HIV-associated tuberculous lymphadenitis.

H Müller1, S Krüger.   

Abstract

Inflammatory cells in lymph nodes of eighteen patients suffering from culture-proven tuberculous lymphadenitis were examined by histological and immunohistochemical techniques. Ten patients suffered from symptomatic HIV-infection and eight patients were immunocompetent individuals without HIV-1 serology. Characteristic granulomas with or without caseation were observed in eight immunocompetent and four HIV-1-infected patients with less marked lymphopenia of CD4 positive peripheral blood lymphocytes. No epitheloid cell formation was present in lymph nodes of HIV1-infected patients with more severe depression of CD4 positive peripheral blood lymphocyte count. Foamy macrophages were found instead of these cells. While many cells--predominantly lymphocytes--express CD25 (IL-2 receptor) in cases with typical epitheloid granulomas there is no such CD25 expression in cases without any epitheloid cell formation. This result suggest that T cell function is necessary for epitheloid granuloma formation in human tuberculosis. The phenotype of macrophages underwent progressive changes parallel to decreasing numbers of CD4 positive peripheral blood lymphocytes. Foamy macrophages in Mycobacterium avium-intracellulare infection represented an end-stage phenotype. They were positive for S100 protein and they did not express lysozyme, alpha-1-anti-chymotrypsin, L1 antigen (Mac387) and CD4, whereas positivity for HLA-DR, CD68 and Ki-M8 was preserved. In situ immunohistochemical demonstration of IFN-alpha, IFN-beta, TNF-alpha, IL-1 and IL-6 revealed that foamy cells in M. tuberculosis infection were highly active effector cells. They contained higher concentrations of the examined cytokines than epitheloid cells in the lesions of HIV+ and HIV-patients. Corresponding to these findings the histological proof of acid-fast bacilli was generally not successful in typical HIV-associated tuberculosis. The foamy appearance may result from the lipid-rich cell membranes of destroyed acid-fast bacilli. In contrast acid-fast bacilli-packed foamy macrophages in AIDS patients with M. avium-intracellulare (MAI) infection did not produce any of the examined cytokines.

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Year:  1994        PMID: 7713549     DOI: 10.1016/S0171-2985(11)80441-9

Source DB:  PubMed          Journal:  Immunobiology        ISSN: 0171-2985            Impact factor:   3.144


  12 in total

1.  Can an immunohistochemistry method differentiate intestinal tuberculosis from Crohn's disease in biopsy specimens?

Authors:  Ali Tüzün Ince; Pembegül Güneş; Ebubekir Senateş; Mesut Sezikli; Arzu Tiftikçi; Oya Ovünç
Journal:  Dig Dis Sci       Date:  2010-09-08       Impact factor: 3.199

2.  Beta-chemokines are induced by Mycobacterium tuberculosis and inhibit its growth.

Authors:  Jussi J Saukkonen; Beth Bazydlo; Michael Thomas; Robert M Strieter; Joseph Keane; Hardy Kornfeld
Journal:  Infect Immun       Date:  2002-04       Impact factor: 3.441

3.  Mycobacterium tuberculosis diverts alpha interferon-induced monocyte differentiation from dendritic cells into immunoprivileged macrophage-like host cells.

Authors:  Sabrina Mariotti; Raffaela Teloni; Elisabetta Iona; Lanfranco Fattorini; Giulia Romagnoli; Maria Cristina Gagliardi; Graziella Orefici; Roberto Nisini
Journal:  Infect Immun       Date:  2004-08       Impact factor: 3.441

4.  Reversible lipid accumulation and associated division arrest of Mycobacterium avium in lipoprotein-induced foamy macrophages may resemble key events during latency and reactivation of tuberculosis.

Authors:  Irène Caire-Brändli; Alexia Papadopoulos; Wladimir Malaga; David Marais; Stéphane Canaan; Lutz Thilo; Chantal de Chastellier
Journal:  Infect Immun       Date:  2013-11-25       Impact factor: 3.441

5.  Adaptation of Mycobacterium tuberculosis to Impaired Host Immunity in HIV-Infected Patients.

Authors:  Nicholas D Walter; Bouke C de Jong; Benjamin J Garcia; Gregory M Dolganov; William Worodria; Patrick Byanyima; Emmanuel Musisi; Laurence Huang; Edward D Chan; Tran T Van; Martin Antonio; Abigail Ayorinde; Midori Kato-Maeda; Payam Nahid; Ann M Leung; Andrew Yen; Tasha E Fingerlin; Katerina Kechris; Michael Strong; Martin I Voskuil; J Lucian Davis; Gary K Schoolnik
Journal:  J Infect Dis       Date:  2016-08-17       Impact factor: 5.226

6.  Carboxypeptidase-M is regulated by lipids and CSFs in macrophages and dendritic cells and expressed selectively in tissue granulomas and foam cells.

Authors:  Ioannis Tsakiris; Daniel Torocsik; Adrienn Gyongyosi; Aniko Dozsa; Istvan Szatmari; Attila Szanto; Gyorgyike Soos; Zoltan Nemes; Laszlo Igali; Ildiko Marton; Zoltan Takats; Laszlo Nagy; Balazs Dezso
Journal:  Lab Invest       Date:  2011-12-12       Impact factor: 5.662

Review 7.  The tuberculous granuloma: an unsuccessful host defence mechanism providing a safety shelter for the bacteria?

Authors:  Mayra Silva Miranda; Adrien Breiman; Sophie Allain; Florence Deknuydt; Frederic Altare
Journal:  Clin Dev Immunol       Date:  2012-07-03

8.  Depletion of CD4(+) T cells causes reactivation of murine persistent tuberculosis despite continued expression of interferon gamma and nitric oxide synthase 2.

Authors:  C A Scanga; V P Mohan; K Yu; H Joseph; K Tanaka; J Chan; J L Flynn
Journal:  J Exp Med       Date:  2000-08-07       Impact factor: 14.307

9.  Alphabeta T cell receptor-positive cells and interferon-gamma, but not inducible nitric oxide synthase, are critical for granuloma necrosis in a mouse model of mycobacteria-induced pulmonary immunopathology.

Authors:  S Ehlers; J Benini; H D Held; C Roeck; G Alber; S Uhlig
Journal:  J Exp Med       Date:  2001-12-17       Impact factor: 14.307

10.  Foamy macrophages from tuberculous patients' granulomas constitute a nutrient-rich reservoir for M. tuberculosis persistence.

Authors:  Pascale Peyron; Julien Vaubourgeix; Yannick Poquet; Florence Levillain; Catherine Botanch; Fabienne Bardou; Mamadou Daffé; Jean-François Emile; Bruno Marchou; Pere-Joan Cardona; Chantal de Chastellier; Frédéric Altare
Journal:  PLoS Pathog       Date:  2008-11-11       Impact factor: 6.823

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