Interferon-γ: the Major Mediator of Resistance Against Toxoplasma gondii

American Association for the Advancement of Science (AAAS) - Tập 240 Số 4851 - Trang 516-518 - 1988
Yasuhiro Suzuki1, Manuel Orellana1, Robert D. Schreiber2,3, Jack S. Remington1
1Department of Immunology and Infectious Diseases, Research Institute, Palo Alto Medical Foundation, CA 94301 and Department of Medicine, Division of Infectious Diseases, Stanford University School of Medicine, Stanford, CA 94305.
2Departnent of Pathology, Washington University School of Medicine, St. Louis, MO 63130.
3Immunobiology

Tóm tắt

Mice were injected with a monoclonal antibody to interferon-γ to examine the importance of endogenous production of this lymphokine in resistance against infection with the sporozoan parasite Toxoplasma gondii . Mice with intraperitoneal infections of T. gondii that received no antibody survived and developed chronic T. gondii infection, whereas the infected mice that received the monoclonal antibody died of toxoplasmosis. The activation of macrophages, which kill T. gondii in vivo, was inhibited by administration of the monoclonal antibody, but the production of antibodies to T. gondii was not suppressed. The fact that an antibody to interferon-γ can eliminate resistance to acute Toxoplasma infection in mice suggests that this lymphokine is an important mediator of host resistance to this parasite.

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Tài liệu tham khảo

ANDERSON, S.E., JOURNAL OF EXPERIMENTAL MEDICINE 139: 1154 (1974).

BLACK, C.M., INVIVO AND INVITRO ACTIVATION OF ALVEOLAR MACROPHAGES BY RECOMBINANT INTERFERON-GAMMA, JOURNAL OF IMMUNOLOGY 138: 491 (1987).

BOWEN, D.L., IMMUNOPATHOGENESIS OF THE ACQUIRED IMMUNODEFICIENCY SYNDROME, ANNALS OF INTERNAL MEDICINE 103: 704 (1985).

BUCHMEIER, N.A., REQUIREMENT OF ENDOGENOUS INTERFERON-GAMMA PRODUCTION FOR RESOLUTION OF LISTERIA-MONOCYTOGENES INFECTION, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 82: 7404 (1985).

DESMONTS, G, DIRECT AGGLUTINATION-TEST FOR DIAGNOSIS OF TOXOPLASMA INFECTION - METHOD FOR INCREASING SENSITIVITY AND SPECIFICITY, JOURNAL OF CLINICAL MICROBIOLOGY 11: 562 (1980).

FOSTER, B.G., STUDIES OF ACTIVE AND PASSIVE IMMUNITY IN ANIMALS INOCULATED WITH TOXOPLASMA GONDII, CANADIAN JOURNAL OF MICROBIOLOGY 14: 103 (1968).

FRENKEL, J.K., ADOPTIVE IMMUNITY OT INTRACELLULAR INFECTION, JOURNAL OF IMMUNOLOGY 98: 1309 (1967).

HIBBS, J. B., NATURE-NEW BIOLOGY 235: 48 (1972).

10.1126/science.177.4053.998

HOFF, R. L., JOURNAL OF EXPERIMENTAL MEDICINE 139: 560 (1974).

JACOBS, L, PROPAGATION, MORPHOLOGY, AND BIOLOGY OF TOXOPLASMA, ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 64: 154 (1956).

JONES, T.C., ASSESSMENT INVITRO OF IMMUNITY AGAINST TOXOPLASMA-GONDII, JOURNAL OF EXPERIMENTAL MEDICINE 141: 466 (1975).

Krahenbuhl, J. L., Immunology of Parasitic Infections: 356 (1982).

MCCABE, R.E., EFFECT OF MURINE INTERFERON GAMMA ON MURINE TOXOPLASMOSIS, JOURNAL OF INFECTIOUS DISEASES 150: 961 (1984).

McLeod, R., Methods for Studying Mononuclear Phagocytes: 709 (1981).

MURRAY, H.W., MACROPHAGE OXYGEN-DEPENDENT ANTI-MICROBIAL ACTIVITY .3. ENHANCED OXIDATIVE-METABOLISM AS AN EXPRESSION OF MACROPHAGE ACTIVATION, JOURNAL OF EXPERIMENTAL MEDICINE 152: 1596 (1980).

MURRAY, H.W., ACTIVATION OF MOUSE PERITONEAL-MACROPHAGES INVITRO AND INVIVO BY INTERFERON-GAMMA, JOURNAL OF IMMUNOLOGY 134: 1619 (1985).

MURRAY, H.W., J IMMUNOL 135: 3274 (1985).

MURRAY, H.W., IMPAIRED PRODUCTION OF LYMPHOKINES AND IMMUNE (GAMMA) INTERFERON IN THE ACQUIRED IMMUNODEFICIENCY SYNDROME, NEW ENGLAND JOURNAL OF MEDICINE 310: 883 (1984).

NACY, C.A., MACROPHAGE ACTIVATION TO KILL LEISHMANIA MAJOR - ACTIVATION OF MACROPHAGES FOR INTRACELLULAR DESTRUCTION OF AMASTIGOTES CAN BE INDUCED BY BOTH RECOMBINANT INTERFERON-GAMMA AND NON-INTERFERON LYMPHOKINES, JOURNAL OF IMMUNOLOGY 135: 3505 (1985).

NAKAYAMA, I, KEIO J MED 14: 63 (1965).

NATHAN, C.F., IDENTIFICATION OF INTERFERON-GAMMA AS THE LYMPHOKINE THAT ACTIVATES HUMAN MACROPHAGE OXIDATIVE-METABOLISM AND ANTI-MICROBIAL ACTIVITY, JOURNAL OF EXPERIMENTAL MEDICINE 158: 670 (1983).

NATHAN, C.F., MECHANISMS HOST RESI: 165 (1986).

PAVIA, C.S., PROTECTION AGAINST EXPERIMENTAL TOXOPLASMOSIS BY ADOPTIVE IMMUNOTHERAPY, JOURNAL OF IMMUNOLOGY 137: 2985 (1986).

Pfefferkorn, E. R., Proceedings of the National Academy of Sciences of the United States of America 81: 908 (1984).

REMINGTON, J.S., ROLE FOR ACTIVATED MACROPHAGES IN RESISTANCE TO INFECTION WITH TOXOPLASMA, INFECTION AND IMMUNITY 6: 829 (1972).

RUSKIN, J, STUDIES ON MECHANISMS OF RESISTANCE TO PHYLOGENTICALLY DIVERSE INTRACELLULAR ORGANISMS, JOURNAL OF IMMUNOLOGY 103: 252 (1969).

10.1038/330664a0

SCHREIBER, R.D., MONOCLONAL-ANTIBODIES TO MURINE GAMMA-INTERFERON WHICH DIFFERENTIALLY MODULATE MACROPHAGE ACTIVATION AND ANTIVIRAL ACTIVITY, JOURNAL OF IMMUNOLOGY 134: 1609 (1985).

Suzuki, Y., Journal of Immunology 140: 3943 (1988).

SUZUKI Y unpublished data.

TURCO, J, GAMMA-INTERFERON-INDUCED INHIBITION OF THE GROWTH OF RICKETTSIA-PROWAZEKII IN FIBROBLASTS CANNOT BE EXPLAINED BY THE DEGRADATION OF TRYPTOPHAN OR OTHER AMINO-ACIDS, INFECTION AND IMMUNITY 53: 38 (1986).

WILDFUHR, G, Z IMMUNITAETSFORSCH 113: 435 (1957).

WILSON, C.B., ACTIVATION OF NEONATAL AND ADULT HUMAN MACROPHAGES BY ALPHA-INTERFERON, BETA-INTERFERON, AND GAMMA-INTERFERON, INFECTION AND IMMUNITY 49: 351 (1985).