SDZ MRL 953, a novel immunostimulatory monosaccharidic lipid A analog with an improved therapeutic window in experimental sepsis

SDZ MRL 953, a new synthetic monosaccharidic lipid A, was investigated in vitro and in vivo for immunopharmacological activities. In experimental models of microbial infections, the compound was highly protective when it was administered prophylactically either once or three times to myelosuppressed or immunocompetent mice. The 50% effective doses of SDZ MRL 953 varied with the infectious agents and the route of its administration. In all cases, the 50% effective doses were about 10(3) times higher than those obtained with endotoxin from Salmonella abortus equi. SDZ MRL 953 was, however, less toxic than lipopolysaccharide by a factor of 10(4) to greater than 7 x 10(5) times in galactosamine-sensitized mice. The compound was also an effective inducer of tolerance to endotoxin. Hence, repeated dosing with the compound induced a transient resistance (greater than or equal to 1 week) to lethal challenges with endotoxin. In vitro, the compound was devoid of intrinsic antimicrobial activity, but it moderately induced the release of cytokines from monocytes and primed human neutrophils for the enhanced production of reactive oxygen metabolites in response to a soluble stimulus. The results presented here suggest that SDZ MRL 953 may be useful in a clinical setting for enhancing resistance to infections, particularly in patients undergoing myelosuppressive chemotherapy or irradiation, and for the prophylaxis of endotoxin shock.

[1]  J. Hildebrandt,et al.  Highly purified lipid X is devoid of immunostimulatory activity. Isolation and characterization of immunostimulating contaminants in a batch of synthetic lipid X. , 1990, The Journal of biological chemistry.

[2]  S. Ikeda,et al.  Antiherpes activity of chemically synthesized lipid A-subunit analogue GLA-60 in immunosuppressed mice. , 1989, Antiviral research.

[3]  Y. Kumazawa,et al.  [Studies on lipid A, the active center of endotoxin--structure-activity relationship]. , 1989, Nihon saikingaku zasshi. Japanese journal of bacteriology.

[4]  S. Ikeda,et al.  Enhancement of nonspecific resistance to viral infection by chemically synthesized lipid A-subunit analogs with different backbone structures and acyl groups. , 1988, Antiviral research.

[5]  E. N. Kaufman,et al.  Recombinant interleukin-1 alpha and recombinant tumor necrosis factor alpha synergize in vivo to induce early endotoxin tolerance and associated hematopoietic changes , 1988, Infection and immunity.

[6]  D. Golenbock,et al.  Lipid X protects mice against fatal Escherichia coli infection , 1988, Infection and immunity.

[7]  M. Kiso,et al.  Importance of fatty acid substituents of chemically synthesized lipid A-subunit analogs in the expression of immunopharmacological activity , 1988, Infection and immunity.

[8]  M. Baggiolini,et al.  Chemiluminescence detection of H2O2 produced by human neutrophils during the respiratory burst. , 1987, Analytical biochemistry.

[9]  T. Ōhashi,et al.  Enhanced resistance of mice to bacterial infection induced by recombinant human interleukin-1a , 1987, Infection and immunity.

[10]  T. Sayers,et al.  The production of tumor necrosis factor by mouse bone marrow-derived macrophages in response to bacterial lipopolysaccharide and a chemically synthesized monosaccharide precursor. , 1987, Journal of immunology.

[11]  I. Macher A convenient synthesis of 2-deoxy-2-[(R)-1-hydroxytetradecanamido]-3-O-[(R)-3-hydroxytetradecanoyl]-α-d-glucopyranose 1-phosphate (lipid X) , 1987 .

[12]  T. Ogawa,et al.  Requirement of a properly acylated beta(1-6)-D-glucosamine disaccharide bisphosphate structure for efficient manifestation of full endotoxic and associated bioactivities of lipid A , 1987, Infection and immunity.

[13]  E. Rietschel,et al.  Lipid A, the endotoxic center of bacterial lipopolysaccharides: relation of chemical structure to biological activity. , 1987, Progress in clinical and biological research.

[14]  Y. Ogawa,et al.  Synthesis of 2-deoxy-4-O-phosphono-3-O-tetradecanoyl-2-[(3R)- and (3S)-3-tetradecanoyloxytetradecanamido]-D-glucose: a diastereoisomeric pair of 4-O-phosphono-D-glucosamine derivatives (GLA-27) related to bacterial lipid A. , 1986, Carbohydrate research.

[15]  C. Haslett,et al.  Neutrophil-mediated injury to endothelial cells. Enhancement by endotoxin and essential role of neutrophil elastase. , 1986, The Journal of clinical investigation.

[16]  G. Pier,et al.  Efficacy of intravenous immune globulin for treatment of experimental pseudomonas aeruginosa pneumonia , 1986 .

[17]  R. Urbaschek,et al.  Induction of Nonspecific Resistance and Stimulation of Granulopoiesis by Endotoxins and Nontoxic Bacterial Cell Wall Components and Their Passive Transfer , 1985, Annals of the New York Academy of Sciences.

[18]  S. Kusumoto,et al.  Total synthesis of escherichia coli lipid A , 1985 .

[19]  L. Mcphail,et al.  Priming of neutrophils for enhanced release of oxygen metabolites by bacterial lipopolysaccharide. Evidence for increased activity of the superoxide-producing enzyme , 1984, The Journal of experimental medicine.

[20]  E. Ribi Beneficial modification of the endotoxin molecule. , 1984, Journal of biological response modifiers.

[21]  C. Raetz,et al.  Glucosamine-derived phospholipids in Escherichia coli. Structure and chemical modification of a triacyl glucosamine 1-phosphate found in a phosphatidylglycerol-deficient mutant. , 1983, The Journal of biological chemistry.

[22]  N. Qureshi,et al.  Complete structure of lipid A obtained from the lipopolysaccharides of the heptoseless mutant of Salmonella typhimurium. , 1983, The Journal of biological chemistry.

[23]  T. Iwashita,et al.  Chemical structure of E. Coli Lipid A: Linkage site of acyl groups in the disaccharide backbone , 1983 .

[24]  W. Reutter,et al.  Galactosamine-induced sensitization to the lethal effects of endotoxin. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[25]  J. Grogan,et al.  Suppression of Reticuloendothelial Function in the Rat with Cyclophosphamide , 1969, Journal of bacteriology.

[26]  A. Nowotny Endotoxoid Preparations , 1963, Nature.

[27]  M. Tainter,et al.  Estimation of the ED50 and Its Error by Means of Logarithmic-Probit Graph Paper.∗ , 1944 .

[28]  A. Hirschfelder THE UNITED STATES PHARMACOPEIAL CONVENTION , 1930 .