The effects of HIV viral load on the phagocytic activity of monocytes activated with lipopolysaccharide from oral microorganisms

Immunopharmacology and Immunotoxicology

Volumn 21, Issue 3, 1999, Pages 421-438

  Baqui, A A M A ^a   Meiller, Timothy F ^a   Zhang, Ming ^a   Falkler Jr , William A ^a  

^a UNIVERSITY OF MARYLAND DENTAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BACTERIUM LIPOPOLYSACCHARIDE; COMPLEMENT COMPONENT C3B RECEPTOR; EDETIC ACID; FLUORESCEIN ISOTHIOCYANATE;

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FUSOBACTERIUM NUCLEATUM; HUMAN; HUMAN CELL; HUMAN IMMUNODEFICIENCY VIRUS 1; IMMUNOHISTOCHEMISTRY; INFECTION SENSITIVITY; LEUKOCYTE ACTIVATION; MALE; MONOCYTE; MOUTH FLORA; OPPORTUNISTIC INFECTION; PHAGOCYTOSIS; PORPHYROMONAS GINGIVALIS; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SACCHAROMYCES; VIRUS LOAD;

BACTERIA (MICROORGANISMS); FUSOBACTERIUM NUCLEATUM; HUMAN IMMUNODEFICIENCY VIRUS; HUMAN IMMUNODEFICIENCY VIRUS 1; PORPHYROMONAS GINGIVALIS; SACCHAROMYCES;

EID: 0032845278     PISSN: 08923973     EISSN: None     Source Type: Journal    
DOI: 10.3109/08923979909007118     Document Type: Article

References (40)

1. Tetali, S., Bakshi, S., Pahwa, S., Abrams, E., Romano, J., Pahwa, S. G. Plasma virus load evaluation in relation to disease progression in HIV-infected children. AIDS Res. Hum. Retroviruses , 14:571, 1998.
2. Mellors, J. W., Jr., C. R. R., Gupta, P., White, R. M., Todd, J. A., Kingsley, L. A. Prognosis in HIV-1 infection predicted by the quantity of virus in plasma. Sci., 272:1167, 1996.
3. Caliendo, A. M. Methods, Interpretation and Application of HIV-1 Viral Load Measurements. Clin. Microbiol. Newslett., 19:1, 1997.
4. Moore, W. E. C., Holdeman, L. V., Cato, E. P., Smibert, R. M., Burmeister, J. A., Raney, R. R. Bacteriology of moderate (chronic) periodontitis in mature adult humans. Infect. Immun., 42:510, 1983.
5. Dzink, J. L., Socransky, S. S., Haffajee, A. D. The predominant cultiviable microbiota of active and inactive lesions of destructive periodontal disease. J. Clin. Periodontol., 15:316, 1988.
6. Moore, W. E. C., Holdeman, L. V., Cato, E. P., et al. Comparative bacteriology of juvenile periodontitis Infect Immun., 48:507, 1985.
7. Moore, W. E. C., Moore, L. V. H., Ranney, R. R., Smibert, R. M., Burmeister, J. A., Schenkein, H. A. The microflora of periodontal sites showing active destructive progression. J. Clin. Periodontol., 18:729, 1991.
8. Baqui, A. A. M. A., Meiller, T. F., Turng, B.-F., Kelley, J. I., William A. Falkler, J. Functional changes in THP-1 human monocytic cells after stimulation with lipopolysaccharide of oral microorganisms and granulocyte macrophage colony stimulating factor Imrnunopharmacol. Immunotoxicol., 20:493, 1998c.
9. Baqui, A. A. M. A., Meiller, T. F., Chon, J. J., Turng, B.-F., Falkler Jr., W. A. Granulocyte-macrophage colony-stimulating factor amplification of Interleukin 1 beta and Tumor necrosis factor alpha production in THP-1 human monocytic cells stimulated with lipopolysaccharide of oral microorganisms. Clin. Diagn Lab. Immunol., 5:341, 1998a.
10. Baqui, A. A. M. A., Meiller, T. F., Chon, J. J., Turng, B.-F., Falkler Jr., W. A. Interleukin-6 production by human monocytes treated with granulocyte-macrophage colony-stimulating factor in the presence of oral microorganisms. Oral Microbiol. Immunol., 13:173, 1998b.
11. Westphal, O., Jahn, K. Bacterial lipopolysaccharides. Extraction with phenol-water and further applications of the procedure. Methods Carbohydr. Chem., 5:83, 1965.
12. Tomoda, T., Kurashige, T., Taniguchi, T. Inhibition of interferon-gamma- and phorbol ester-induced HLA-DR and interleukin-1 production by the expression of a transfected poly(ADP-ribose) synthetase gene in human leukemia THP-1 cells. Biochim. Biophys. Acta, 1135:79, 1992.
13. Lundahl, J., Hallden, G., Hallgren, M., Skold, C. M., Hed, J. Altered expression of CD11b/CD18 and CD62L on human monocytes after cell preparation procedures. J. Immunol. Methods, 180:93, 1995.
14. Lee, Y.-J., Benvenniste, E. N. Stat 1-alpha expressions is involved in IFN-gamma induction of the class II transactivator and class II MHC genes. J. Immunol., 157:1559, 1996.
15. Boutten, A., Dehoux, M., Deschenes, M., Rouzeau, J.-D., Bories, P. N., Durand, G. Alpha 1-acid glycoprotein potentiates lipoppolysaccharide-induced secretion of interleukin-1 beta, interleukin-6 and tumor necrosis factor-alpha by human monocytes and alveolar and peritoneal macrophages. Eur. J. Immunol., 22:2687, 1992.
16. Nathan, C. F. Secretory products of macrophages J. Clin. Invest., 79:319, 1987.
17. Fujiwara, T., Ogawa, T., Sobue, S., Hamada, S. Chemical, immunobiological and antigenic characterizations of lipopolysaccharides from Bacteroides gingivalis strains. J. Gen. Microbiol., 136:319, 1990.
18. Hamada, S., Koga, T., Nishihara, T., Fujiwara, T., Okahashi, N. Characterization and immunobiologic activities of lipopolysaccharides from periodontal bacteria. Adv. Dent. Res., 2:284, 1988.
19. Wan, C. P., Park, C. S., Lau, B. H. S. A rapid and simple microfluorometric phagocytosis assay. J. Immunol. Methods, 162:1, 1993.
20. Andoh, A., Fujiyama, Y., Kitoh, K., Hodohara, K., Bamba, T., Hosoda, S. Flow cytometric assay for phagocytosis of human monocytes mediated via Fc gamma-receptors and complement receptor CR1 (CD35). Cytometry, 12:677, 1991.
21. Drevets, D. A., Campbell, P. A. Macrophage phagocytosis: use of fluorescence microscopy to distinguish between extracellular and intracellular bacteria. J. Immunol. Methods, 142:31, 1991.
22. Fattorossi, A., Nisini, R., Pizzolo, J. G., D'Amelio, R. New, simple flow cytometry technique to discriminate between internalized and membrane-bound particles in phagocytosis. Cytometry, 10:320, 1989.
23. Flo, R. W., Naess, A., Nilsen, A., Harthug, S., Solberg, C. O. A longitudinal study of phagocytic function in HIV-infected patients. AIDS, 8:771, 1994.
24. Crowe, S. M., Vardzxis, N. J., Kent, S. J., et al. HIV infection of monocyte-derived macrophages in vitro reduces phagocytosis of Candida albicans. J. Leukocyte Biol, 56:318, 1994.
25. Capsoni, F., Minonzio, F., Ongari, A. M., Rizzardi, G. P., Lazzarin, A., Zanussi, C. Monocyte-derived macrophage function in HIV-infected subjects: in vitro modulation by rIFN-gamma and rGM-CSF. Clinical Immunol. Immunopathol, 62:176, 1992.
26. Baldwin, G. C., Fleischmann, J., Chung, Y., Koyanagi, Y., Chen, I. S. Y., Golde, D. W. Human immunodeficiency virus causes mononuclear phagocyte dysfunction. Proc. Nat. Acad. Sci. USA, 87:3933, 1990.
27. Musher, D. M., Watson, D. A., Nickeson, D., Gyorkey, F., Lahart, C., Rossen, R. D. The effect of HIV infection on phagocytosis and killing of Staphylococcus aureus by human pulmonary alveolar macrophages. Am. J. Med. Sci., 299:158, 1990.
28. Poli, G., Bottazzi, B., Acero, R., et al. Monocyte function in intravenous drug abusers with lymphadenopathy syndrome and in patients with acquired immunodeficiency syndrome: selective impairment of chemotaxis. Clin. Exp. Immunol., 62:136, 1985.
29. Roux-Lombard, P., Aladjem, D., Belavoine, J.-F., et al. Altered functions of peripheral blood monocytes in homosexual males and intravenous drug users with persistent lymphadenopathy. Eur. J. Clin. Invest., 16:262, 1986.
30. Nielsen, H., Kharazmi, A., Faber, V. Blood monocyte and neutrophil functions in the acquired immune deficiency syndrome. Scand. J. Immunol., 24:291, 1986.
31. Nottet, H. S. L. M., de Graaf L., de Vos, N. M., et al. Phagocytic function of monocyte-derived macrophages is not affected by human immunodeficiency virus type I infection. J. Infect Dis., 168:84, 1993.
32. Szkjaradkiewicz, A. Phagocytosis and microbiocidal capacity of human monocytes in the course of HIV infection. Immunol. Lett., 33:145, 1992.
33. Bandres, J. C., Trial, J., Musher, D. M., Rossen, R. D. Increased phagocytosis and generation of reactive oxygen products by neutrophils and monocytes of men with stage 1 human immunodeficiency virus infection. J. Infect. Dis., 168:75, 1993.
34. Pos, O., Stevenhagen, A., Meenhorst, P. L., Kroon, F. P., van Furth, R. Impaired phagocytosis of Staphylococcus aureus by granulocytes and monocytes of AIDS patients. Clin. Exp. Immunol., 88:23, 1992.
35. Roilides, E., Holmes, A., Blake, C., Pizzo, P. A., Walsh, T. J. Defective antifungal activity of monocyte-derived macrophages from human immunodeficiency virus-infected children against Aspergillus fumigatus. J. Infect. Dis., 168:1562, 1993.
36. Daar, E. S., Moudgil, T., Meyer, M. S., Ho, D. D. Transient high levels of viremia in patients with primary human immunodeficiency virus type 1 infection. New Eng. J. Med., 324:961, 1991.
37. Connor, R. I., Mohri, H., Cao, Y., Ho, D. D. Increased viral burden and cytopathicity correlate temporally with CD4+ T lymphocyte decline and clinical progression in human immunodeficiency virus type-1 infected individuals. J. Virol., 67:1772, 1993.
38. Kesson, A., Fear, W., Kazazi, F., et al. Human immunodeficiency virus type 1 infection of placental macrophages. J. Infect. Dis., 168:571, 1993.
39. Sierra-Madero, J. G., Toossi, Z , Hom, D. L., Finegan, C. K., Hoenig, E., Rich, E. A. Relationship between load of virus in alveolar macrophages from human immunodeficiency virus type-1 infected persons, production of cytokines and clinical status. J. Infect. Dis., 169:18, 1994.
40. Kent, S. J., Stent, G., Sonza, S., Hunter, S. D., Crowe, S. M. HIV-1 infection of monocyte-derived macrophages reduces Fc and complement receptor expression. Clin. Exp. Immunol., 95:450, 1994.