Alveolar macrophage priming by intravenous administration of chitin particles, polymers of N-acetyl-D-glucosamine, in mice

Infection and Immunity

Volumn 65, Issue 5, 1997, Pages 1734-1741

  Shibata, Yoshimi ^a   Foster, L Ann ^b   Metzger, W James ^a   Myrvik, Quentin N ^c  

^a EAST CAROLINA UNIVERSITY   (United States)

^b Southern College of SDA   (United States)

^c Myrvik Enterprises   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHITIN; CHITOSAN; GAMMA INTERFERON; N ACETYLGLUCOSAMINE; PHORBOL 13 ACETATE 12 MYRISTATE;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL CULTURE; CELLULAR IMMUNITY; FLOW CYTOMETRY; IMMUNE RESPONSE; LISTERIA MONOCYTOGENES; LUNG ALVEOLUS MACROPHAGE; MOUSE; MYCOBACTERIUM TUBERCULOSIS; NATURAL KILLER CELL; NONHUMAN; PHAGOCYTOSIS; PRIORITY JOURNAL; RECEPTOR UPREGULATION; RESPIRATORY BURST; SCID MOUSE; SPLEEN CELL;

EID: 0030901437     PISSN: 00199567     EISSN: None     Source Type: Journal    
DOI: 10.1128/iai.65.5.1734-1741.1997     Document Type: Article

References (44)

1. Allen, L.-A. H., and A. Aderem. 1995. A role of MARCKS, the α isozyme of protein kinase C and myosin I in zymosan phagocytosis by macrophages. J. Exp. Med. 182:829-840.
2. Azuma, I. 1992. Synthetic immunoadjuvants: application to non-specific host stimulation and potentiation of vaccine immunogenicity. Vaccine 10:1000-1006.
3. Bautista, A. P., A. Schuler, Z. Spolarics, and J. J. Spitzer. 1992. In vivo late phagocytosis primes the Kupffer cells and hepatic neutrophils to generate superoxide anion. J. Leukocyte Biol. 51:39-45.
4. 2 inhibits production of Th1 lymphokines but not of Th2 lymphokines. J. Immunol. 146:108-113.
5. Black, C. M., J. R. Catterall, and J. S. Remington. 1987. In vivo and in vitro activation of alveolar macrophages by recombinant interferon-γ. J. Immunol. 138:491-195.
6. Bourbouze, R., R. Raffi, G. Dameron, H. Hali-Miraftab, F. Loko, and J.-L. Vilde. 1991. N-Acetyl-β-D-glycosaminidase (NAG) isozymes released from human monocytes-derived macrophages in response to zymosan and human recombinant interferon-γ. Clin. Chim. Acta 199:185-194.
7. Buchmeier, N. A., and R. D. Schreiber. 1985. Requirement of endogenous interferon-γ production for resolution of Listeria monocytogenes infection. Proc. Natl. Acad. Sci. USA 82:7404-7408.
8. Chida, K., Q. N. Myrvik, E. S. Leake, M. R. Gordon, P. H. Wood, and M. J. Ricardo Jr. 1987. Chemiluminescent responses of alveolar macrophages from normal and Mycobacterium bovis BCG-vaccinated rabbits as a function of age. Infect. Immun. 55:1476-1483.
9. Cooper, A. M., D. K. Dalton, T. A. Stewart, J. P. Griffin, D. G. Russell, and I. M., Orme. 1994. Disseminated tuberculosis in interferon γ gene-disrupted mice. J. Exp. Med. 178:2243-2247.
10. Corradin, S. B., and J. Mauel. 1991. Phagocytosis of Leishmania enhances macrophage activation by IFN-γ and lipopolysaccharide. J. Immunol. 146: 279-285.
11. Debono, M., and R. S. Gordee. 1994. Antibiotics that inhibit fungal cell wall development. Annu. Rev. Microbiol. 48:471-497.
12. Dunn, P. L., and R. J. North. 1991. Early gamma interferon production by natural killer cells is important in defense against murine listeriosis. Infect. Immun. 59:2892-2900.
13. Flynn, J. L., J. Chan, K. J. Triebold, D. K. Dalton, T. A. Stewart, and B. R. Bloom. 1994. An essential role for interferon γ in resistance to Mycobacterium tuberculosis infection. J. Exp. Med. 178:2249-2254.
14. Hayakawa, H., K. Umehara, and Q. N. Myrvik. 1988. Oxidative responses of rabbit alveolar macrophages: comparative priming activities of MIF/MAF, sera, and serum components. J. Leukocyte Biol. 45:231-238.
15. Hirano, S., M. Iwata, K. Yamanaka, H. Tanaka, T. Toda, and H. Inui. 1991. Enhancement of serum lysozyme activity by injecting a mixture of chitosan oligosaccharides intravenously in rabbits. Agric. Biol. Chem. 55:2623-2625.
16. Hsieh, C. S., A. B. Heimberger, J. S. Gold, A. O'Garra, and K. M. Murphy. 1992. Differential regulation of T helper phenotype development by interleukin 4 and 10 in an alpha-beta T-cell-receptor transgenic system. Proc. Natl. Acad. Sci. USA 89:6065-6069.
17. + through IL-12 produced by Listeria induced macrophages. Science 260:547-549.
18. Johnston, R. B., C. A. Godzik, and Z. A. Cohn. 1978. Increased Superoxide anion production by immunologically activated and chemically elicited macrophages. J. Exp. Med. 148:115-127.
19. Marodi, L., S. Schreiber, D. C. Anderson, R. P. MacDermott, H. M. Korchak, and R. B. Johnston, Jr. 1993. Enhancement of macrophage candidacidal activity by interferon-γ. Increased phagocytosis, killing, and calcium signal mediated by a decreased number of mannose receptors. J. Clin. Invest. 91:2596-2601.
20. Murray, H. W. 1988. Interferon-gamma, the activated macrophage, and host defense against microbial challenge. Ann. Intern. Med. 108:595-608.
21. Myrvik, Q. N., A. G. Gristina, G. Giridhar, and H. Hayakawa. 1993. Particle-induced in vivo priming of alveolar macrophages for enhanced oxidative responses: a novel system of cellular immune augmentation. J. Leukocyte Biol. 54:439-443.
22. Nafsik, H. G., and J. S. Tkacz. 1995. The fungal cell wall as a drug target. Trends Microbiol. 3:98-104.
23. Nathan, C. F., H. W. Murray, M. E. Wiebe, and B. Y. Rubin. 1983. Identification of interferon-γ as the lymphokine that activates human macrophage oxidative metabolism and antimicrobial activity. J. Exp. Med. 158:670-689.
24. Nishimura, K., S. Nishimura, H. Seo, N. Nishi, S. Tokura, and I. Azuma. 1986. Macrophage activation with multi-porous beads prepared from par tially deacetylated chitin. J. Biomed. Mater. Res. 20:1359-1372.
25. Nishimura, K., C. Ishihara, S. Ukei, S. Tokura, and I. Azuma. 1986. Stimulation of cytokine production in mice using deacetylated chitin. Vaccine 4:151-156.
26. Nishimura, K., S. Nishimura, H. Seo, N. Nishi, S. Tokura, and I. Azuma. 1987. Effect of multiporous microspheres derived from chitin and partially deacetylated chitin on the activation of mouse peritoneal macrophages. Vaccine 5:136-140.
27. Okumura, H., H. Tsutsui, T. Komatsu, M. Yutsudo, A. Hakura, T. Tanimoto, K. Torigoe, T. Okura, Y. Nukada, K. Hattori, K. Akita, M. Namba, F. Tanabe, K. Konishi, S. Fukuda, and M. Kurimoto. 1995. Cloning of a new cytokine that induces IFNγ production by T cells. Nature 378:88-91.
28. Pontow, S. E., V. Kery, and P. D. Stahl. 1992. Mannose receptor. Int. Rev. Cytol. 137B:221-244.
29. Powrie, F., S. Menon, and R. L. Coffman. 1993. Interleukin-4 and interleukin-10 synergize to inhibit cell-mediated immunity in vivo. Eur. J. Immunol. 23:3043-3049.
30. Schafer, R., and T. K. Eisenstein. 1992. Natural killer cells mediated protection induced by a Salmonella aroA mutant. Infect. Immun. 60:791-797.
31. Scott, P. 1991. IFN-γ modulates the early development of Th1 and Th2 responses in a murine model of cutaneous leishmaniasis. J. Immunol. 147: 3149-3155.
32. Scott, P. 1993. IL-12: initiation cytokine for cell-mediated immunity. Science 260:496-497.
33. Shibata, Y., and A. Volkman. 1985. The eftect of bone marrow depletion on prostaglandin E producing suppressor macrophages in mouse spleen. J. Immunol. 135:3897-3904.
34. 2. Blood 83:3316-3323.
35. 2 release triggered by phagocytosis of latex beads. A distinct association with prostaglandin synthase isozymes in bone marrow macrophages. J. Immunol. 154:2878-2887.
36. Skeen, M. J., M. A. Miller, T. M. Shinnick, and H. K. Ziegler. 1996. Regulation of murine macrophage IL-12 production. Activation of macrophages in vivo, restimulation in vitro, and modulation by other cytokines. J. Immunol. 156:1196-1206.
37. Snijders, A., C. M. U. Hilkens, C. T. M. van der Pouw Kraan, M. Engel, L. A. Aarden, and M. L. Kapsenberg. 1996. Regulation of bioactive IL-12 production in lipopolysaccharide-stimulated human monocytes is determined by the expression of the p35 subunit. J. Immunol. 156:1207-1212.
38. Stepherd, V. L., Y. C. Lee, P. H. Schlesinger, and P. D. Stahl. 1981. L-Fucose-terminated glycoconjugates are recognized by pinocytosis receptors on macrophages. Proc. Natl. Acad. Sci. USA 78:1019-1022.
39. Tripp, C. S., M. K. Gately, J. Hakimi, P. Ling, and E. R. Unanue. 1994. Neutralization of IL-12 decreases resistance to Listeria in SCID and C.B-17 mice. J. Immunol. 152:1883-1887.
40. Tripp, C. S., S. F. Wolf, and E. R. Unanue. 1993. Interleukin 12 and tumor necrosis factor α are costimulators of interteron γ production by natural killer cells in severe combined immunodeficiency mice with listeriosis, and interleukin 10 is a physiologic antagonist. Proc. Natl. Acad. Sci. USA 90: 3725-3729.
41. Warr, G. A. 1980. A macrophage receptor for (mannose/glucosamine)-glycoproteins of potential importance in phagocytie activity. Biochem. Biophys. Res. Commun. 93:737-745.
42. Wong, H. L., M. T. Lotze, L. M. Wahl, and S. M. Wahl. 1992. Administration of recombinant IL-4 to humans regulates gene expression, phenotype, and function in circulating monocytes. J. Immunol. 148:2118-2125.
43. Yamamoto, N., J. P. Zou, X. F. Li, H. Takenaka, S. Noda, T. Fujii, S. Ono, Y. Kobayashi, N. Mukaida, K. Matsushima, H. Fujiwara, and T. Hamaoka. 1995. Regulatory mechanisms for production of IFN-γ and TNF by antitumor T cells or macrophages in the tumor-bearing state. J. Immunol. 154: 2281-2290.
44. Yoshihara, R., S. Shiozawa, T. Fujita, and K. Chihara. 1993. Gamma interferon is produced by human natural killer cells but not T cells during Staphylococcus aureus stimulation. Infect. Immun. 61:3117-3122.