Interferon and Its Inducers: Antiviral and Other Effects

References

• Findlay G. M., MacCallum F. O. An interference phenomenon in relation to yellow fever and other viruses. J. Pathol. Bacteriol. 1937; 44: 405
   Google Scholar
• Vilcek J. Interferon. Virology Monographs. Springer-Verlag, New York 1969; 6
   Google Scholar
• Portner A., Kingsbury D. W. Homologous interference by incomplete Sendai virus particles: Changes in virus-specific ribonucleic acid synthesis. J. Virol. 1971; 8: 388
   Google Scholar
• Bratt M. A., Rubin H. Specific interference among strains of Newcastle disease virus. III. Mechanisms of interference. Virology 1968; 35: 395
   Google Scholar
• Pohjanpelto P., Cooper P. D. Interference between polioviruses induced by strains that cannot multiply. Virology 1965; 25: 350
   Google Scholar
• Marcus P. I., Zuckerbraun H. L. Viral polymerase proteins as antiviral agents. Ann. N. Y. Acad. Sci. 1970; 173: 185
   Google Scholar
• Huang A. S., Baltimore D. Defective viral particles and viral disease process. Nature 1970; 226: 325
   Google Scholar
• Marcus P. I., Carver D. H. Intrinsic interference: A new type of viral interference. J. Virol. 1967; 1: 334
   Google Scholar
• Baluda M. A. Loss of viral receptors in homologous interference by ultraviolet-irradiated Newcastle disease virus. Virology 1959; 7: 315
   Google Scholar
• Crowell R. L., Syverton J. T. The mammalian cell-virus relationship. VI. Sustained infection of HeLa cells by Coxsackie B3 virus and effect of superinfection. J. Exp. Med. 1961; 113: 419
   Google Scholar
• Price W. H., Thind J. S., O'Leary W., El Dadah A. A protective mechanism induced by live group B arboviruses against heterologous group B arboviruses independent of serum neutralizing antibodies or interferon. Am. J. Epidemiol. 1967; 86: 11
   PubMed Web of Science ®Google Scholar
• Thind J. S., Price W. H. A new specific humoral viral resistance factor, serum protective factor - some biologic and physical properties. J. Immunol. 1971; 106: 1559
   Google Scholar
• Isaacs A., Lindenmann J. Virus interference. I. The interferon. Proc. R. Soc. Lond. (Biol.) 1957; 147: 258
   PubMed Web of Science ®Google Scholar
• Isaacs A., Lindenmann J., Valentine R. C. Virus interference. II. Some properties of interferon. Proc. R. Soc. Lond. (Biol.) 1957; 147: 268
   PubMed Web of Science ®Google Scholar
• Lindenmann J., Burke D., Isaacs A. Studies on the production, mode of action, and properties of interferon. Br. J. Exp. Pathol. 1957; 38: 551
   PubMedGoogle Scholar
• Grossberg S. E. The interferons and their inducers: Molecular and therapeutic considerations. N. Engl. J. Med., in press
   Google Scholar
• DeClercq E., Merigan T. C. Current concepts of interferon and interferon induction. Ann. Rev. Med. 1970; 21: 17
   Google Scholar
• Wagner R. R., Smith T. J. The interferons: some unsolved problems of action and biosynthesis. Int. Conf. on Vaccine against Viral and Rickettsial Diseases of Man. 1st Pan-Am. Health Organ., Washington, DC 1967; 616
   Google Scholar
• Ho M., Postic B. Prospects for applying interferon to man. Int. Conf. on Vaccine against Viral and Rickettsial Diseases of Man. 1st Pan-Am. Health Organ., Washington, DC 1967; 632
   Google Scholar
• Merigan T. C. Various molecular species of interferon induced by viral and nonviral agents. Bacteriol. Rev. 1967; 31: 138
   Google Scholar
• Paucker K., Boxaca M. Cellular resistance to induction of interferon. Bacteriol. Rev. 1967; 31: 145
   Google Scholar
• Burke D. C., Skehel J. J. Interferons and other cell products influencing viral multiplication. Br. Med. Bull. 1967; 23: 109
   Google Scholar
• Lockart R. Z., Jr. Recent progress in research on interferons. Progr. Med. Virol. 1967; 9: 451
   Google Scholar
• Wheelock E. F., Larke R. P. B., Caroline N. L. Interference in human viral infections: Present status and prospects for the future. Progr. Med. Virol. 1968; 10: 286
   PubMedGoogle Scholar
• Hilleman M. R. Interferon induction and utilization. J. Cell. Physiol. 1968; 71: 43
   Google Scholar
• Finkelstein M. S., Merigan T. C. Interferon 1968 - how much do we understand. Calif. Med. 1968; 109: 24
   PubMedGoogle Scholar
• Tytell A. A., Field A. K. Interferon and host resistance with particular emphasis on induction by complexed polynucleotides. CRC Crit. Rev. Biochem., in press
   Google Scholar
• Colby C., Morgan M. J. Interferon induction and action. Ann. Rev. Microbiol. 1971; 25: 333
   Google Scholar
• Merigan T. C. Interferon stimulated by double-stranded RNA. Nature 1970; 228: 219
   Google Scholar
• Strander H. Production of interferon by suspended human leukocytes, Dissertation for the degree of Doctor of Medicine. Karolinska Institute, StockholmSweden 1971
   Google Scholar
• Myers M. W., Friedman R. M. Potentiation of human interferon production by superinduction. J. Natl. Cancer Inst. 1971; 47: 757
   Google Scholar
• Isaacs A. Interferon. Sci. Am. 1961; 204: 51
   Google Scholar
• Isaacs A. Mechanisms of virus infections. Nature 1961; 192: 1247
   Google Scholar
• Rotem Z., Cox R. A., Isaacs A. Inhibition of virus multiplication by foreign nucleic acid. Nature 1963; 197: 564
   PubMedGoogle Scholar
• Isaacs A., Cox R. A., Rotem Z. Foreign nucleic acids as the stimulus to make interferon. Lancet 1963; 2: 113
   PubMed Web of Science ®Google Scholar
• Youngner J. S., Stinebring W. R. Interferon production in chickens injected with Brucella abortus. Science 1964; 144: 1022
   Google Scholar
• Stinebring W. R., Youngner J. S. Patterns of interferon appearance in mice injected with bacteria or bacterial endotoxin. Nature 1964; 204: 712
   PubMed Web of Science ®Google Scholar
• Ho M. Interferon-like viral inhibition in rabbits after intravenous administration of endotoxin. Science 1964; 146: 1472
   PubMed Web of Science ®Google Scholar
• Field A. K., Tytell A. A., Lampson G. P., Hilleman M. R. Inducers of interferon and host resistance. II. Multistranded synthetic polynucleotide complexes. Proc. Natl. Acad. Sci. USA 1967; 58: 1004
   PubMed Web of Science ®Google Scholar
• Merigan T. C. Interferon induction in mice and man with viral and non-viral stimuli. Ciba Found. Symp. Interferon, G. E. W. Wolstenholme, M. O'Conner. Little, Brown, & Co., Boston 1967; 50
   Google Scholar
• DeClercq E., Merigan T. C. Induction of interferon by nonviral agents. Arch. Intern. Med. 1970; 126: 94
   Google Scholar
• Schmidthe J. R., Johnson E. G. Regulation of the immune system by synthetic polynucleotides. I. Characteristics of adjuvant action on antibody synthesis. J. Immunol. 1971; 106: 1191
   Google Scholar
• Johnson H. G., Johnson E. G. Regulation of the immune system by synthetic polynucleotides. II. Action on peritoneal exudate cells. J. Exp. Med. 1971; 133: 649
   Google Scholar
• Cone R. E., Johnson E. G. Regulation of the immune system by synthetic polynucleotides. III. Action on antigen-reactive cells of thymic origin. J. Exp. Med. 1971; 133: 665
   PubMed Web of Science ®Google Scholar
• Campbell P. A., Kind P. Bone marrow-derived cells as target cells for polynucleotide adjuvants. J. Immunol. 1971; 107: 1419
   Google Scholar
• Claes P., Billiau A., DeClercq E., Desmyter J., Schonne E., Vanderhaegle H., DeSomer P. Polyacetal carboxylic acids: a new group of antiviral polyanions. J. Virol. 1970; 5: 313
   PubMed Web of Science ®Google Scholar
• Billiau A., Desmyter J., DeSomer P. Antiviral activity of chlorite-oxidized oxyamylose, a polyacetal carboxylic acid. J. Virol. 1970; 5: 321
   PubMed Web of Science ®Google Scholar
• Billiau A., Muyembe J. J., DeSomer P. Effect of chlorite-oxidized oxyamylose on influenza virus infection in mice. Appl. Microbiol. 1971; 21: 580
   PubMedGoogle Scholar
• Billiau A., Muyembe J. J., DeSomer P. Mechanism of antiviral activity in vivo of polycarboxylates which induce interferon production. Nature New Biol. 1971; 232: 183
   Google Scholar
• Billiau A., Eyser H., David G., DeSomer P. Adjuvant activity of polyacetal carboxylates for antibody induction in mice and guinea pigs. Proc. Soc. Exp. Biol. Med. 1971; 137: 626
   Google Scholar
• Lampson G. P., Field A. K., Tytell A. A., Nemes M. M., Hilleman M. R. Relationship of molecular size of rIn:rCn (Poly 1:C) to induction of interferon and host resistance. Proc. Soc. Exp. Biol. Med. 1970; 135: 911
   PubMed Web of Science ®Google Scholar
• Tytell A. A., Lampson G. P., Field A. K., Nemes M. M., Hilleman M. R. Influence of size of individual homopolynucleotides on the physical and biological properties of complexed rIn:rCn (Poly I:C). Proc. Soc. Exp. Biol. Med. 1970; 135: 917
   PubMed Web of Science ®Google Scholar
• Niblack J. F., McCreary M. B. Relationship of biological activities of poly I : poly C to homopolymer molecular weights. Nature New Biol. 1971; 233: 53
   Google Scholar
• Phillips B. M., Hartnagel R. E., Kraus P. J., Tamayo R. P., Fonesca E. H., Kowalski R. L. Systemic toxicity of polyinosinic:polycytidylic acid in rodents and dogs. Toxicol. Appl. Pharmacol. 1971; 18: 220
   PubMed Web of Science ®Google Scholar
• Pekarek R. S. Effect of synthetic double-stranded RNA on serum metals in the rat, rabbit, and monkey. Proc. Soc. Exp. Biol. Med. 1971; 136: 584
   Google Scholar
• Alexander P., Evan R. Endotoxin and double-stranded RNA render macrophages cytotoxic. Nature New Biol. 1971; 232: 74
   Google Scholar
• Jullien P., De Maeyer-Guignard J. Toxic effect of polyriboinosinic-polyribocytidylic acid on mouse hemopoietic stem cells. Int. J. Cancer 1971; 7: 468
   Google Scholar
• Yu M. C., Young P. A., Hu Y. H. A. Ultrastructural changes in chick cerebellum induced by polyinosinic-polycytidylic acid. Am. J. Pathol. 1971; 64: 305
   Google Scholar
• Berry L. J., Smythe D. S., Colwell S. S., Schoengold R. J., Actor P. Comparison of the effect of a synthetic polyribonucleotide with the effects of endotoxin on selected host responses. Infect. Immun. 1971; 3: 444
   PubMedGoogle Scholar
• Cox C. G., Rafter G. W. Pyrogen and enzyme release from rabbit blood leukocytes promoted by endotoxin and polyinosinic-polycytidylic acid. Biochem. Med. 1971; 5: 227
   Google Scholar
• Pieroni R. E., Bundeally E. E., Levine L. The effect of actinomycin D on the lethality of poly I:C. J. Immunol. 1971; 106: 1128
   Google Scholar
• Baugh C. L., Tytell A. A., Hilleman M. R. In Vitro safety assessment of double-stranded polynucleotides poly I:C and MU-9. Proc. Soc. Exp. Biol. Med. 1971; 137: 1194
   Google Scholar
• Field A. K., Young C. W., Krakoff I. H., Tytell A. A., Lampson G. P., Nemes M. M., Hilleman M. R. Induction of interferon in human subjects by poly I:C. Proc. Soc. Exp. Biol. Med. 1971; 136: 1180
   PubMed Web of Science ®Google Scholar
• Dianzani F., Cantagalli P., Gagnoni S., Rita G. Effect of DEAE-dextran on production of interferon induced by synthetic double-stranded RNA in L cell cultures. Proc. Soc. Exp. Biol. Med. 1968; 128: 708
   Google Scholar
• Dianzani F., Baron S., Buckler C. E., Levy H. B. Mechanism of DEAE-dextran enhancement of polynucleotide induction of interferon. Proc. Soc. Exp. Biol. Med. 1971; 136: 1111
   PubMed Web of Science ®Google Scholar
• Pitha P. M., Carter W. A. The DEAE-dextran polyriboinosinate-polyribocytidylate complex: physical properties and interferon induction. Virology 1971; 45: 777
   Google Scholar
• Rice J. M., Turner W., Chirigos M. A., Spahn G. Dose responsiveness and variation among inbred strains of mice in production of interferon after treatment with poly (I) : poly (C) (poly-D-lysine) complexes. Appl. Microbiol. 1971; 22: 380
   Google Scholar
• Pitha J., Pitha P. M. Antiviral resistance by the polyinosinic acid poly (I-vinylcytosine) complex. Science 1971; 172: 1146
   Google Scholar
• Pitha P. M., Carter W. A., Pitha J. Antiviral resistance produced by the polyinosinic acid poly (1-vinylcytosine) complex. Int. Colloquium on Interferon and Interferon inducers, LeuvenBelgium 1971
   Google Scholar
• Beck G., Ebel J. P., Louisot P., Gresle J., Pradal M. B., Colobert L. Inhibition of viral multiplication by chemically methylated DNA from the host cell. Nature 1970; 228: 859
   Google Scholar
• Youngner J. S., Stinebring W. R., Taube S. E. Influence of inhibitors of protein synthesis on interferon formation in mice. Virology 1965; 27: 541
   Google Scholar
• Lukas B., Hruskova J. In vivo induction of an interferon-like inhibitor by kanamycin. Acta Virol. (Praha) 1968; 12: 263
   Google Scholar
• Krueger R. F., Meyer G. D. Tilorone hydrochloride: an orally active antiviral agent. Science 1970; 169: 1213
   PubMed Web of Science ®Google Scholar
• Mayer G. D., Krueger R. F. Tilorone hydrochloride: mode of action. Science 1970; 169: 1214
   PubMed Web of Science ®Google Scholar
• DeClercq E., Merigan T. C. Bis-DEAE-fluorenone: mechanism of antiviral protection and stimulation of interferon production in the mouse. J. Infect. Dis. 1971; 123: 190
   Google Scholar
• Kaufman H. E., Centifanto Y. M., Elleson E. D., Brown D. C. Tilorone hydrochloride: human toxicity and interferon stimulation. Proc. Soc. Exp. Biol. Med. 1971; 137: 357
   Google Scholar
• Degre M., Dahl H. Protection of an interferon-like agent following inoculation with bacterial vaccine. Proc. Soc. Exp. Biol. Med. 1971; 137: 233
   Google Scholar
• Singer J. H., Hardegree M. C. Induction of interferon by bacterial vaccines and allergenic extracts. J. Allergy 1971; 47: 332
   Google Scholar
• Kojima Y., Homma J. Y., Abe C. Property to induce interferon of Pseudomonas aeruginosa endotoxin and its components. Jap. J. Exp. Med. 1971; 41: 493
   Google Scholar
• Feingold D. S., Youngner J. S., Chen J. Interferon production in mice by cell wall mutants of Salmonella typhimurium. III. Role of lipid moiety of bacterial lipopolysaccharide in interferon production in animals. Ann. N. Y. Acad. Sci. 1970; 173: 249
   Google Scholar
• VonFrank R. M., Ellis L. F., Kleinschmidt W. J. Purification and physical properties of mycophage PSI. J. Gen. Virol. 1971; 12: 33
   Google Scholar
• Banks G. T., Buck K. W., Chain E. B., Darbyshie J. E., Himmelweit F., Ratti G., Sharpe T. J., Planterose D. N. Antiviral activity of double-stranded RNA isolated from Aspergillus foetidus. Nature 1970; 227: 505
   Google Scholar
• Buck K. W., Chain E. B., Himmelweit F. Comparison of interferon induction in mice by purified Penicillium chrysogenum virus and derived double-stranded RNA. J. Gen. Virol. 1971; 12: 131
   Google Scholar
• Stern R., Friedman R. M. Ribonucleic acid synthesis in animal cells in the presence of actinomycin. Biochemistry 1971; 10: 3635
   Google Scholar
• Pindak F. F., Schmidt J. P., Giron D. J., Allen P. T. Interferon levels and resistance to viral infections associated with selected interferon inducers. Proc. Soc. Exp. Biol. Med. 1971; 138: 317
   PubMed Web of Science ®Google Scholar
• DeClercq E., Nuwer M. R., Merigan T. C. The role of interferon in the protective effect of a synthetic double-stranded polyribonucleotide against intranasal vesicular stomatitis virus challenge in mice. J. Clin. Invest. 1970; 49: 1565
   Google Scholar
• Burke D. C. Mechanisms of interferon production. Interferons, N. B. Finter. North Holland Pub. Co., Amsterdam 1966; 55
   Google Scholar
• Jacob F., Monod J. Genetic regulatory mechanisms in the synthesis of proteins. J. Mol. Biol. 1961; 3: 318
   PubMed Web of Science ®Google Scholar
• Ho M., Kono Y. Effect of actinomycin D on virus and endotoxin induced interferon-like inhibitors in rabbits. Proc. Natl. Acad. Sci. USA 1965; 53: 220
   Google Scholar
• Finkelstein M. S., Bausek G., Merigan T. C. Interferon inducers in vitro: difference in sensitivity to inhibitors of RNA and protein synthesis. Science 1970; 161: 465
   Google Scholar
• Bausek G. H., Merigan T. C. Cell interaction with a synthetic polynucleotide and interferon production in vitro. Virology 1969; 39: 491
   PubMed Web of Science ®Google Scholar
• Schell P. L. Uptake of polynucleotides by intact mammalian cells (IV): synthetic homopolyribonucleotides. Z. Naturforsch. 1968; 23b: 1117
   Google Scholar
• DeClercq E., Wells R. D., Grant R. C., Merigan T. C. Thermal activation of the antiviral activity of synthetic double-stranded polyribonucleotides. J. Mol. Biol. 1971; 56: 83
   Google Scholar
• DeClercq E., DeSomer P. Antiviral activity of polyribocytidylic acid in cells primed with polyriboinosinic acid. Science 1971; 173: 260
   Google Scholar
• DeClercq E., DeSomer P. Mechanism of the priming effect of poly (rI) on the antiviral activity of poly (rC). Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Wagner H. F., Bugianesi R. L., Shen T. Y. Preparation of Sepharose-bound poly (rI:rC). Biochem. Biophys. Res. Commun. 1971; 45: 184
   PubMed Web of Science ®Google Scholar
• Long W. F., Burke D. C. Interferon production by double-stranded RNA: a comparison of induction by reovirus to that by a synthetic double-stranded polynucleotide. J. Gen. Virol. 1971; 12: 1
   PubMedGoogle Scholar
• Clavell L. A., Bratt M. A. Relationship between the ribonucleic acid-synthesizing capacity of ultraviolet-irradiated Newcastle disease virus and its ability to induce interferon. J. Virol. 1971; 8: 500
   Google Scholar
• Meager A., Burke D. C. Interferon production by ultraviolet-radiation inactivated Newcastle disease virus. Nature 1972; 235: 280
   Google Scholar
• Lockart R. Z., Jr., Bayliss N. L., Toy S. T., Yin F. H. Viral events necessary for the induction of interferon in chick embryo cells. J. Virol. 1968; 2: 962
   PubMed Web of Science ®Google Scholar
• Burke D. C. The production of interferon by animal viruses. Proc. R. Soc. Lond. (Biol.) 1971; 177: 17
   Google Scholar
• Oie H. K., Loh P. C. Reovirus type 2: induction of viral resistance and interferon production in fathead minnow cells. Proc. Soc. Exp. Biol. Med. 1971; 136: 369
   PubMed Web of Science ®Google Scholar
• Lanez G. J., Johnson T. C. Biochemical events during interferon synthesis in L cells infected with Newcastle disease virus. Proc. Soc. Exp. Biol. Med. 1971; 136: 1078
   Google Scholar
• Nemes M. M., Tytell A. A., Lampson G. P., Field A. K., Hilleman M. R. Inducers of interferon and host resistance. VII. Antiviral efficacy of double-stranded RNA of natural origin. Proc. Soc. Exp. Biol. Med. 1969; 132: 784
   Google Scholar
• Colby C., Stollar B. D., Simon M. I. Interferon induction: DNA-RNA hybrid or double-stranded RNA. Nature New Biol. 1971; 229: 172
   PubMedGoogle Scholar
• Steinberg A. D., Baron S., Ullendorf C., Talal N. Depression of the interferon response to polyinosinicpolycytidylic acid by specific antibody. Proc. Soc. Exp. Biol. Med. 1971; 137: 558
   Google Scholar
• Markovits P., Coppey J. Studies on interferon induction by avian adenovirus in chicken cells. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Goorha R. M., Gifford G. E. Comparison of interferon induction by active and inactive Semliki Forest virus. J. Gen. Virol. 1971; 10: 117
   Google Scholar
• Best J. M., Banatvala J. E., Smith M. E. Further studies on the growth of rubella virus in human embryonic organ cultures: preliminary observations on interferon production in these cultures. J. Hyg. (Camb.) 1971; 69: 223
   Google Scholar
• De Maeyer E., De Maeyer-Guignard J., Montagnier L. Double-stranded RNA from rat liver induces interferon in rat cells. Nature New Biol. 1971; 229: 109
   Google Scholar
• Stewart W. E., II, Gosser L. B., Lockart R. Z., Jr. Distinguishing characteristics of the interferon response of primary and continuous mouse cell cultures. J. Gen. Virol. 1971; 13: 35
   Google Scholar
• Stewart W. E., II, Gosser L. B., Lockart R. Z., Jr. Priming: a nonantiviral function of interferon. J. Virol. 1971; 7: 792
   PubMedGoogle Scholar
• Stewart W. E., II, Lockart R. Z., Jr. Interferon production in interferon-treated cells: blocking. priming, and interferon potentials of cells. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Tan Y. H., Armstrong J. A., Ho M. Accentuation on interferon production by metabolic inhibitors and its dependence on protein synthesis. Virology 1971; 44: 503
   Google Scholar
• Ke Y. H., Ho M. Patterns of cycloheximide and puromycin effect on interferon production stimulated by virus or polyribonucleotide in different tissues. Proc. Soc. Exp. Biol. Med. 1971; 136: 365
   PubMed Web of Science ®Google Scholar
• Vicek J., Ng M. H. Post-transcriptional control of interferon synthesis. J. Virol. 1971; 7: 588
   Google Scholar
• Friedman R. M., Myers M. W. Potentiation of human interferon production by superinduction. J. Natl. Cancer Inst. 1971; 47: 757
   Google Scholar
• Marrs B. L., Yanofsky C. Host and bacteriophage specific messenger RNA degradation in T7-infected Escherichia coli. Nature New Biol. 1971; 234: 168
   Google Scholar
• Tan Y. H., Armstrong J. A., Ho M. Intracellular interferon: kinetics of formation and release. Virology 1971; 45: 837
   Google Scholar
• Ho M., Tan Y. H., Ke Y. A., Armstrong J. A. Studies on the induction and release of interferon. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Kohno S., Kohase M., Sakata H., Shmizu Y. Inhibition of interferon synthesis in phospholipase C treated primary chick embryo cells. Virology 1971; 44: 227
   Google Scholar
• Waschke J., Lackovic V., Borecky L. Relation of incubation temperature to interferon production in mouse peritoneal cells infected with Newcastle disease virus. Acta Virol. 1969; 13: 387
   Google Scholar
• De Maeyer-Guignard J., De Maeyer E. Effect of antilymphocytic serum on circulating interferon in mice as a function of the inducer. Nature New Biol. 1971; 229: 212
   Google Scholar
• Absher M., Stinebring W. R. Effect of sheep antilymphocyte serum on immune production of interferon in tuberculin sensitive mice. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Friedman R. M., Barth R. F., Stern R. Anomalous effect of heterologous normal serum on interferon production in mice. Nature New Biol. 1971; 230: 17
   Google Scholar
• De Maeyer E., Fauve R. M., De Maeyer-Guignard J. Production d'interferon au niveau du macrophage. Ann. Inst. Pasteur, Paris 1971; 120: 438
   Google Scholar
• Epstein L. B., Cline M. J., Merigan T. C. In vitro interaction of macrophages and lymphocytes in the antigen (PPD)-induced production of interferon. Proc. 6th Leukocyte Culture Conf., M. R. Schwartz. Academic Press, New York 1972, in press
   Google Scholar
• Glasgow L. A., Odugbeni T., Dwyer P., Ritterson A. L. Eperythrozoon coccoides. I. Effect on the interferon response in mice. Infect. Immun. 1971; 4: 425
   Google Scholar
• Ito Y., Kunii A., Mori N., Nagata I. Effect of splenectomy on production of endotoxin-type interferon in mice. Virology 1971; 44: 638
   Google Scholar
• Mendelson J., Dick V. Production of interferon by murine peritoneal leukocytes: enhancement by mineral oil. J. Infect. Dis. 1971; 123: 351
   Google Scholar
• DeClercq E., Nuwer M. R., Merigan T. C. Potentiating effect of Freund's adjuvant on interferon production by endotoxin or poly rI: poly rC. Infect. Immun. 1970; 2: 69
   Google Scholar
• Gifford G. E., Tibor A., Peavy D. L. Interferon production in mixed lymphocyte cell cultures. Infect. Immun. 1971; 3: 164
   PubMedGoogle Scholar
• Moehring J. M., Stinebring W. R., Merchant D. J. Survey of interferon production in human cell lines. Appl. Microbiol. 1971; 22: 102
   Google Scholar
• Carter W. A., Hande K. R., Essien B., Prochownik E., Kaback M. M. Comparative production of interferon by human fetal, neonatal, and maternal cells. Infect. Immun. 1971; 3: 671
   Google Scholar
• De Maeyer E., De Maeyer-Guignard J. Quantitative control of interferon in mice. Int. Colloquium on interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Cassingena R., Chany C., Vignal M., Suarcz H., Estrade S., Lazar P. Use of monkey-mouse hybrid cells for the study of cellular regulation of interferon production and action. Proc. Natl. Acad. Sci. USA 1971; 68: 580
   PubMed Web of Science ®Google Scholar
• Chany C., Cassingena R. Investigations on the genetic location governing the synthesis of interferon and the antiviral protein. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Bausek G. H., Merigan T. C. Two mechanisms of cell resistance to stimulation of interferon. Proc. Soc. Exp. Biol. Med. 1970; 134: 672
   Google Scholar
• Chester T. J., De Clercq E., Merigan T. C. Effect of separate and combined injections of poly rI: poly rC and endotoxin on reticuloendothelial activity, interferon, and antibody production in the mouse. Infect. Immun. 1971; 3: 516
   Google Scholar
• Du Buy H. G., Johnson M. L., Buckler C. E., Baron S. Relationship between dose size and dose interval of polyinosinic-polycytidylic acid and interferon hyporesponsiveness in mice. Proc. Soc. Exp. Biol. Med. 1970; 135: 340
   Google Scholar
• Buckler C. E., Du Buy H. G., Johnson M. L., Baron S. Kinetics of serum interferon response in mice after single and multiple injections of poly I: poly C. Proc. Soc. Exp. Biol. Med. 1971; 136: 394
   PubMed Web of Science ®Google Scholar
• Bordon E. C., Murphy F. A. The interferon refractory state: in vivo and in vitro studies. J. Immunol. 1971; 106: 134
   Google Scholar
• Sharpe T. J., Birch P. J., Planterose D. N. Resistance to virus infection during the hyporeactive state of interferon induction. J. Gen. Virol. 1971; 12: 331
   Google Scholar
• Dianzani R., Neri P., Zucca F. Effect of cyclic-AMP on interferon production by L cells induced with poly I: poly C or NDV. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Fantes K. H. Heterogeneity and other physico-chemical properties of interferons. Int. Colloquium on Interferon and Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Paucker K., Berman B. J., Golgher R. R., Stancek D. Purification, characterization and attempted labeling of mouse interferon. J. Virol. 1970; 5: 145
   Google Scholar
• Stancek D., Paucker K. Preparative electrophoresis of isotopically labeled L-cell interferons. Appl. Microbiol. 1971; 21: 1067
   Google Scholar
• Yamazaki S., Wagner R. R. Purified rabbit interferon: Attempts to demonstrate interferon-specific 3H-protein. J. Virol. 1970; 5: 270
   Google Scholar
• Carter W. A. Interferon: evidence for subunit structure. Proc. Natl. Acad. Sci. USA 1970; 67: 620
   PubMed Web of Science ®Google Scholar
• Carter W. A. Purification of mouse and human interferons, detection of subunit structure. Prep. Biochem. 1971; 1: 55
   PubMed Web of Science ®Google Scholar
• Carter W. A., Pitha P. M., Marshall L. W. Interferon: further characterization of oligomeric forms. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Burke D. C., Isaacs A. Interferon: relation to heterologous interference and lack of antigenicity. Acta Virol. 1960; 4: 215
   Google Scholar
• Isaacs A. Interferon. Adv. Virus Res. 1963; 10: 1
   PubMedGoogle Scholar
• Paucker K., Cantell K. Neutralization of interferon by specific antibody. Virology 1962; 18: 145
   Google Scholar
• Paucker K. The serologic specificity of interferon. J. Immunol. 1965; 94: 371
   PubMed Web of Science ®Google Scholar
• Boxaca M., Paucker K. Neutralization of different murine interferons by antibody. J. Immunol. 1967; 98: 1130
   PubMed Web of Science ®Google Scholar
• Fauconnier B. Antigenic identity of interferons induced by different viruses in the same cell system. Nature 1967; 214: 591
   Google Scholar
• Gresser I., Bourali C., Thomas M. T., Falcoff E. Effect of repeated inoculation of interferon preparations on infection of mice with encephalomyocarditis virus. Proc. Soc. Exp. Biol. Med. 1968; 127: 491
   Google Scholar
• Taylor J. Inhibition of interferon action by actinomycin. Biochem. Biophys. Res. Commun. 1964; 14: 447
   PubMed Web of Science ®Google Scholar
• Taylor J. Studies on the mechanism of action of interferon. I. Interferon action and RNA synthesis in chick embryo fibroblasts infected with Semliki Forest virus. Virology 1965; 25: 340
   PubMed Web of Science ®Google Scholar
• Friedman R. M. Interferon binding: the first step in establishment of antiviral activity. Science 1967; 156: 1760
   PubMed Web of Science ®Google Scholar
• Buckler C. E., Baron S., Levy H. B. Interferon: lack of detectable uptake by cells. Science 1966; 152: 80
   PubMed Web of Science ®Google Scholar
• Marcus P. I., Salb J. M. Molecular basis of interferon action: inhibition of viral RNA translation. Virology 1966; 30: 502
   PubMed Web of Science ®Google Scholar
• Carter W. A., Levy H. B. The recognition of viral RNA by mammalian ribosomes, an effect of interferon. Biochim. Biophys. Acta 1968; 155: 437
   Google Scholar
• Kerr I. M., Sonnabead J. A., Martin E. M. Protein-synthetic activity of ribosomes from interferon treated cells. J. Virol. 1970; 5: 132
   Google Scholar
• Kerr I. M. Protein synthesis in cell-free systems: an effect of interferon. J. Virol. 1971; 7: 448
   Google Scholar
• Ken I. M., Martin E. M. Virus protein synthesis in an animal cell-free system: nature of the products synthesized in response to ribonucleic acid of encephalomyocarditis virus. J. Virol. 1971; 7: 438
   Google Scholar
• Armstrong J. A., Freeburg L. C., Ho M. Effect of interferon on synthesis of eastern equine encephalitis virus RNA. Proc. Soc. Exp. Biol. Med. 1971; 137: 13
   Google Scholar
• Oxman M. N., Levin J. M. Interferon and transcription of early virus-specific RNA in cells infected with Simian Virus 40. Proc. Natl. Acad. Sci. USA 1971; 68: 299
   PubMed Web of Science ®Google Scholar
• Marcus P. I., Engelhardt D. L., Hunt J. M., Sekellick M. J. Interferon action: inhibition of vesicular stomatitis virus RNA synthesis induced by virion-bound polymerase. Science 1971; 174: 593
   Google Scholar
• Baltimore D., Huang A. S., Stampfer M. Ribonucleic acid synthesis of vesicular stomatitis virus. II. An RNA polymerase in the virion. Proc. Natl. Acad. Sci USA 1970; 66: 572
   PubMed Web of Science ®Google Scholar
• Bialy H. S., Colby C. Inhibition of vaccinia virus early m-RNA synthesis in interferon treated cells. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Taylor-Papadimitriou J., Spandidos D., Georgatso J. G. An endonuclease associated with preparations of chick interferon. Biochem. Biophys. Res. Commun. 1971; 43: 149
   Google Scholar
• Friedman R. M., Sreevalsan T. Membrane binding of input arbovirus ribonucleic acid: effect of interferon or cycloheximide. J. Virol. 1970; 6: 169
   Google Scholar
• Friedman R. M., Pastan I. Mechanism of action of 2-mercapto-1-(β -4-pyridethyl) benzimidazole: a reversible inhibitor of interferon activity. Proc. Natl. Acad. Sci. USA 1970; 65: 104
   Google Scholar
• Giron D. J., Allen P. T., Pindak F. F., Schmidt J. P. Inhibition by estrone of the antiviral protection and interferon elicited by interferon inducers in mice. Infect. Immun. 1971; 3: 318
   PubMed Web of Science ®Google Scholar
• Grossberg S. E., Morahan P. S. Repression of interferon action: induced dedifferentiation of embryonic cells. Science 1971; 171: 77
   Google Scholar
• Vilcek J., Varacalli F. Sequential suppression by actinomycin D of interferon production and cellular resistance induced by poly I:C. J. Gen. Virol. 1971; 13: 185
   Google Scholar
• Chany C., Fournier F., Rousset S. Potentiation of the antiviral activity of interferon by actinomycin D. Nature New Biol. 1971; 230: 113
   PubMedGoogle Scholar
• Fournier F., Rousset S., Chany C. Investigations on regulatory mechanisms of the antiviral state induced by interferon. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Thiel K. W., Mohanty S. B., Hetrick F. M. Effect of poly I:C on infectious bovine rhinotrachetitis virus in calves. Proc. Soc. Exp. Biol. Med. 1971; 137: 1176
   Google Scholar
• Todd J. D., Volenec F. J., Paton I. M. Interferon in nasal secretions and sera of calves following intranasal inoculation with avirulent IBR virus, in press
   Google Scholar
• Gerone P. J., Hill D. A., Appell L. H., Baron S. Inhibition of respiratory virus infections of mice with aerosols of synthetic double-stranded ribonucleic acid. Infect. Immun. 1971; 3: 323
   Google Scholar
• Kleinschmidt W. J., Streightoff F. Inhibition of influenza virus and interferon response intranasally with statalon. Infect. Immun. 1971; 4: 738
   Google Scholar
• Portnoy J., Merigan T. C. The effect of interferon and interferon inducers on avian influenza. J. Infect. Dis. 1971; 124: 545
   Google Scholar
• Worthington M., Baron S. Late therapy with an interferon stimulator in an arbovirus encephalitis in mice. Proc. Soc. Exp. Biol. Med. 1971; 136: 323
   Google Scholar
• DeClercq E., Merigan T. C. Local and systemic protection by synthetic polyanionic interferon inducer in mice against intranasal vesicular stomatitis virus. J. Gen. Virol. 1969; 5: 359
   Web of Science ®Google Scholar
• Barahona H. H., Melendez L. V. Herpesvirus saimiri: in vitro sensitivity to virus induced interferon and to polyriboinosinic-polyribocytidylic acid. Proc. Soc. Exp. Biol. Med. 1971; 136: 1163
   Google Scholar
• Oh J. O. Sensitivity of types 1 and 2 Herpesvirus hominis to an interferon inducer, poly I:C. Infect. Immun. 1971; 3: 847
   Google Scholar
• Leunen J., Desmyter J., DeSomer P. Effects of oxyamylose and polyacrylic acid on foot-and-mouth disease and hog cholera virus infections. Appl. Microbiol. 1971; 21: 203
   PubMedGoogle Scholar
• Richmond J. Y. Mouse resistance against foot-and-mouth disease virus induced by injections of pyran. Infect. Immun. 1971; 3: 249
   PubMed Web of Science ®Google Scholar
• Fenje P., Postic B. Prophylaxis of experimental rabies with the polyriboinosinic, polyribocytidylic acid complex. J. Infect. Dis. 1971; 123: 426
   Google Scholar
• Postic B., Fenje P. Effect of administered interferon on rabies in rabbits. Appl. Microbiol. 1971; 22: 428
   Google Scholar
• DeClercq E., De Somer P. Comparative study of the efficacy of different forms of interferon therapy in the treatment of mice challenged intranasally with vesicular stomatitis virus. Proc. Soc. Exp. Biol. Med. 1971; 138: 301
   Google Scholar
• Hallum J. V., Thacore H. R., Youngner J. S. Effects of exogenous interferon on L cells persistently infected with Newcastle disease virus. Infect. and Immun. 1972; 5: 145
   Google Scholar
• Henry C. J., Slifkin M. Inhibition of adenovirus type 2 by human and monkey interferon. Proc. Soc. Exp. Biol. Med. 1971; 137: 1432
   Google Scholar
• Gallagher J. G., Khoolyarian N. Sensitivity of adenovirus types 1,3,4,5,8,11, and 18 to human interferon. Proc. Soc. Exp. Biol. Med. 1971; 136: 920
   Google Scholar
• Armstrong R. W., Merigan T. C. Varicella zoster virus: interferon production and comparative interferon sensitivity in human cell cultures. J. Gen. Virol. 1971; 12: 53
   Google Scholar
• Armstrong R. W., Gurwith M. J., Wadell D., Merigan T. C. Cutaneous interferon production in patients with Hodgkin's disease and other cancers infected with varicella or vaccinia infections. N. Engl. J. Med. 1970; 283: 1182
   PubMed Web of Science ®Google Scholar
• Stevens D. A., Merigan T. C. Interferon antibody and other host factors in Herpes zoster. J. Clin. Invest. 1972, in press
   Google Scholar
• Heath R. B. Interferon production in mice with lymphoma. Interferon Scientific Memorandum. June, 1971; 522
   Google Scholar
• Moehring J. M., Forsyth B. R. The role of the interferon system in respiratory syncytial virus infections. Proc. Soc. Exp. Biol. Med. 1971; 138: 1009
   Google Scholar
• Voroshilova M. K. Live enterovirus interferon inducers and their use for prevention of respiratory infections. Interferon Scientific Memorandum. February, 1971; 476
   Google Scholar
• Luby J. P., Stewart W. E., Sulker E., Sanford J. P. Interferon in human infections with St. Louis encephalitis virus. Ann. Intern. Med. 1969; 71: 703
   Google Scholar
• Sanders D. V., Jr., Luby J. P., Sanford J. P., Hull A. R. Suppression of interferon response in lymphocytes from patients with uremia. J. Lab. Clin. Med. 1971; 77: 768
   PubMedGoogle Scholar
• Luby J. P., Sanders C. V., Sulkin S. E. Interferon assay and quantitative virus determinations in a fatal infection in man with Western equine encephalomyelitis virus. Am. J. Trop. Med. Hyg. 1971; 20: 765
   Google Scholar
• Lee S. H. S., Ozere R. L., Van Rooyen C. E. Interferon production by human lymphocytes in vitro. Reduced levels in lymphatic leukemia. Proc. Soc. Exp. Biol. Med. 1966; 122: 32
   PubMed Web of Science ®Google Scholar
• Hadhazy Gy., Gergely L., Toth F. D., Szegedi G y. Comparative study of the interferon production by the leukocytes of healthy and leukemic subjects. Acta Microbiol. Acad. Sci. Hung. 1967; 14: 391
   Google Scholar
• Hadhazy G y., Nagy G y., Gergely L., Balas C s. Interferon producing capacity of white blood cells from patients with polyglobulinemia. Acta Microbiol. Acad. Sci. Hung. 1970; 17: 329
   Google Scholar
• Gergely L., Toth D., Hadhazy G y., Szabo B. Enhanced interferon production in vitro by leucocytes from children with infectious mononucleosis. Acta Microbiol. Acad. Sci. Hung. 1970; 17: 357
   Google Scholar
• Lee S. H. S., Van Rooyen C. E., Ozere R. L. Additional studies of interferon production by human leukemic leukocytes in vitro. Cancer Res. 1969; 29: 645
   Google Scholar
• Bellanti J. A., Catalano L. W., Chamber R. W. Herpes simplex encephalitis: virologic and serologic study of a patient treated with an interferon inducer. J. Pediatr. 1971; 78: 136
   PubMed Web of Science ®Google Scholar
• Smorodintsev A. A., Beare A. S., Bynol M. L., Head B., Tyrell D. A. J. The formation of interferon during acute respiratory infection of volunteers. Arch. Gesamte Virusforsch. 1971; 33: 9
   Google Scholar
• Hill D. A., Walsh G. H., Purcell R. H. Failure to demonstrate circulating interferon during incubation period and acute stage of transfusion associated hepatitis. Proc. Soc. Exp. Biol. Med. 1971; 136: 853
   Google Scholar
• Sueltenfuss E. A., Pollard M. Cytochemical assay of interferon produced by duck hepatitis virus. Science 1963; 139: 595
   Google Scholar
• Hanna L., Merigan T. C., Jawetz E. Inhibition of TRIC agents by virus-induced interferon. Proc. Soc. Exp. Biol. Med. 1966; 122: 417
   PubMed Web of Science ®Google Scholar
• Reinicke V., Mordhorst C. H., Schonne E. In ovo inhibition of growth of TRIC agents by purified species-specific interferon. Acta Pathol. Microbiol. Scand. 1967; 69: 478
   Google Scholar
• Kazar J., Krautwurst P. A., Gordon F. B. Effect of interferon and interferon inducers on infections with a nonviral intracellular microorganism. Rickettsia akari, Infect. Immun. 1971; 3: 819
   Google Scholar
• Kazar J., Gillmore J. D., Gordon F. B. Effect of interferon and interferon inducers on infections with a nonviral intracellular microorganism. Chlamydia trachomatis, Infect. Immun. 1971; 3: 825
   Google Scholar
• Remington J. S., Merigan T. C. Protection of cells infected with an intracellular protozoon (Toxoplasma gondii). Science 1968; 161: 804
   PubMed Web of Science ®Google Scholar
• Jahiel R. I., Vilcek J., Nussenzweig V., Vanderberg J. Interferon inducers protect mice against Plasmodium berghei malaria. Science 1968; 161: 802
   PubMed Web of Science ®Google Scholar
• Oh J. O., O'Connor G. R. Effect of an interferon inducer, poly I:C on acute ocular infection produced by intracameral inoculation of Toxoplasma gondii. Infect. Immun. 1971; 4: 407
   Google Scholar
• Kumar R., Worthington M., Tilles J. G., Abelmann E. The effect of interferon stimulator polyinosinic-polycytidylic acid on experimental Trypenosoma cruzi infection. Proc. Soc. Exp. Biol. Med. 1971; 137: 884
   Google Scholar
• Herman R., Baron S. Immunologic-mediated protection of Trypanosoma congolense-infected mice by polyribonucleotides. Interferon Scientific Memorandum. May, 1971; 516
   Google Scholar
• Rytel M. W., Suntharasamai P. Interferon response and antiparasitic action in Eperythrozoon coccoides infection of mice. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Gober L. L., Friedman-Kien A. E., Havell E. A., Vilcek J. Interferon preparations and poly I : poly C suppress the intracellular growth of Shigella flexneri in cell cultures. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Yabrov A. A. Increase in stability to diphtheria toxin under the influence of latent viral infection. Tsitologiya 1966; 8: 767
   Google Scholar
• Yabrov A. A. Nonspecific stability of cells to bacterial toxins. Tsitologiya 1967; 9: 692
   Google Scholar
• Moehring T. J., Moehring J. M., Stinebring W. R. Response of interferon treated cells to diphtheria toxin. Infect. Immun. 1971; 4: 747
   Google Scholar
• Gresser I., Copey J., Falcoff E., Fontaine D. Interferon and murine leukemia. I. Inhibitory effect of interferon preparations on development of Friend leukemia in mice. Proc. Soc. Exp. Biol. Med. 1967; 124: 84
   PubMedGoogle Scholar
• Young C. W. Interferon induction in cancer with some observations on the clinical effects of poly I:C. Med. Clin. North Am. 1971; 55: 721
   Google Scholar
• Adamson R. H. Antitumor activity of tilorone hydrochloride against some rodent tumors, preliminary report. J. Natl. Cancer Inst. 1971; 46: 431
   Google Scholar
• Billiau A., Leyten R., Vandeputte M., DeSomer P. Inhibition of development of mammary tumors in C3H mice by neonatal administration of polycarboxylates. Life Sci. 1971; 10: 643
   Web of Science ®Google Scholar
• Kapila K., Smith C., Rubin A. A. Effect of pyran co-polymer on phagocytosis and tumor growth. J. Reticuloendothel. Soc. 1971; 9: 447
   PubMedGoogle Scholar
• Wheelock E. F., Toy S. T. Suppression of established Friend virus leukemia by statalon. IV. Role of interferon and antibody in the development of a dormant infection. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Gelboin H. V., Levy H. B. Polyinosinic-polycytidylic acid inhibits chemically induced tumorigenesis in mouse skin. Science 1970; 167: 205
   PubMed Web of Science ®Google Scholar
• Ball J. K., McCarter J. A. Effect of polyinosinic-polycytidylic acid on induction of primary or transplanted tumors by chemical carcinogens or irradiation. J. Natl. Cancer Inst. 1971; 46: 1009
   Google Scholar
• Sarma P. S., Newbauer R. H., Rabstein L. S. Murine sarcoma and leukemia viral infections of mice: effect of long-term treatment with poly I : poly C. Proc. Soc. Exp. Biol. Med. 1971; 137: 469
   Google Scholar
• Gazdar A. F., Steinberg A. D., Baron S. Enhancement of viral oncogenesis by interferon inducers. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• DeClercq E., Merigan T. C. Moloney sarcoma virus-induced tumors in mice: inhibition or stimulation by (poly rI) - (poly rC). Proc. Soc. Exp. Biol. Med. 1971; 137: 590
   Google Scholar
• Weinstein A. J., Gazdar A. F., Sims H. L., Levy H. B. Lack of correlation between interferon induction and antitumor effect of poly I: poly C. Nature New Biol. 1971; 231: 53
   Google Scholar
• Barker A. D., Rheims M. S., Wilson H. E. Amelioration of Friend virus leukemia by sequential administration of viral and nonviral interferon inducers. Proc. Soc. Exp. Biol. Med. 1971; 137: 981
   Google Scholar
• Rhim J. S., Huebner R. J. Comparison of the antitumor effect of interferon and interferon inducers. Proc. Soc. Exp. Biol. Med. 1971; 136: 524
   PubMedGoogle Scholar
• Lieberman M., Merigan T. C., Kaplan H. S. Inhibition of radiogenic lymphoma development in mice by interferon. Proc. Soc. Exp. Biol. Med. 1971; 138: 575
   Google Scholar
• Came P. E., Moore D. H. Inhibition of spontaneous mammary carcinoma of mice by treatment with interferon and poly I:C. Proc. Soc. Exp. Biol. Med. 1971; 137: 304
   PubMed Web of Science ®Google Scholar
• Padnos M., Shimonaski G., Came P. E. Interferon in mice acutely infected with M-P virus. J. Gen. Virol. 1971; 13: 163
   Google Scholar
• Gresser L., Thomas M. T., Brouty-Boye D., Macieira-Coelho A. Effect of interferon treatment of L1210 cells in vitro on tumor and colony formation. Nature New Biol. 1971; 231: 20
   PubMedGoogle Scholar
• Gresser L., Brouty-Boye D., Thomas M. T., Macieira-Coelho A. Interferon and cell division. I. Inhibition of the multiplication of mouse leukemia L1210 cells in vitro by interferon preparations. Proc. Natl. Acad. Sci. USA 1970; 66: 1052
   PubMed Web of Science ®Google Scholar
• Macieira-Coelho A., Brouty-Boye D., Thomas M. T., Gresser I. Interferon and cell division. III. Effect of interferon on the division of L1210 cells in vitro. J. Cell Biol. 1971; 48: 415
   PubMedGoogle Scholar
• Gresser I., Thomas M. T., Brouty-Boye D., Macieira-Coelho A. Interferon and cell division. V. Titration of the anticellular action of interferon preparations. Proc. Soc. Exp. Biol. Med. 1971; 137: 1258
   PubMedGoogle Scholar
• Taylor-Papadimitriou J., Stoker M. Effect of interferon on some aspects of transformation by polyoma virus. Nature New Biol. 1971; 230: 114
   Google Scholar
• Worthington M., Aaronson S. A. Interferon systems in cells from human tumors and from persons predisposed to cancer. Infect. Immun. 1971; 3: 424
   Google Scholar
• Freeman A. E., Uhlendor C. P., Younkers P. E., Baron S. Responsiveness of normal and transformed rat embryo cell cultures to poly I: poly C and interferon. J. Cell. Physiol. 1970; 76: 365
   Google Scholar
• Moehring J. M., Stinebring W. R. Prolonged application of interferon and “aging” of human diploid fibrolasts. Proc. Soc. Exp. Biol. Med. 1971; 137: 191
   Google Scholar
• Jahiel R. I., Taylor D., Rainford N., Hirschberg S. E., Kromar R. Inducers of interferon inhibit the mitotic response of liver cells to partial hepatectomy. Proc. Natl. Acad. Sci. USA 1971; 68: 740
   Google Scholar
• Jahiel R. I. Effect of interferon inducers on liver cell division. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Lindahl P., Leary P., Gresser I. Inhibitory effect of interferon preparations on the multiplication of normal mouse cells. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• Lindahl-Magnuseon P., Leary P., Gresser I. Interferon and cell division. VI. Inhibitory effect of interferon on the multiplication of mouse embryo and mouse kidney cells in primary culture. Proc. Soc. Exp. Biol. Med. 1971; 138: 1044
   Google Scholar
• Paucker K. Growth inhibition of noninfected L cells by purified mouse interferon. Interferon Scientific Memorandum. September, 1971; 580
   Google Scholar
• Lee S. H. S., O'Shaughnessy M. V., Rozee K. R. Cellular growth inhibition by homologous interferon. Interferon Scientific Memorandum. August, 1971; 569
   Google Scholar
• Rozee K. R., Lee S. H. S., O'Shaughnessy M. V. Interferon inhibition of DNA synthesis and cell division. Interferon Scientific Memorandum. October, 1971; 591
   Google Scholar
• McNeill T. A., Fleming W. A., Killen M. Interferon inhibition of haemopoietic colony growth in vitro. Int. Colloquium on Interferon and Interferon Inducers, LeuvenBelgium 1971
   Google Scholar
• McNeill T. A., Fleming W. A. The relationship between serum interferon and an inhibitor of mouse haemopoietic colonies in vitro. Immunology 1971; 21: 761
   Google Scholar
• McNeill T. A., Killen M. The effect of synthetic double-stranded polyribonucleotides on haemopoietic colony-forming cells in vivo. Immunology 1971; 21: 751
   Google Scholar
• McNeill T. A. The effect of synthetic double-stranded polyribonucleotides on haemopoietic colony-forming cells in vitro. Immunology 1971; 21: 741
   Google Scholar
• Lindahl-Magnusson P., Leary P., Gresser I. Interferon and lymphocytes. Inhibition of DNA synthesis induced by PHA or by allogeneic cells. Interferon Scientific Memorandum. November, 1971; 593
   Google Scholar
• Glasgow L. A. Leukocytes and interferon in the host response to viral infection. II. Enhanced interferon response of leukocytes from immune animals. J. Bacteriol. 1966; 91: 2185
   PubMedGoogle Scholar
• Green J. A., Cooperband S. R., Kibrick S. Immune specific induction of interferon in cultures of human blood lymphocytes. Science 1969; 164: 1415
   PubMed Web of Science ®Google Scholar
• Monath T. P. C., Bordon E. C. Effects of thorotrast on humoral antibody, viral multiplication, and interferon during infection with St. Louis encephalitis virus in mice. J. Infect. Dis. 1971; 123: 297
   Google Scholar
• Worthington M., Baron S. Effectiveness of an interferon stimulator in immunosuppressed mice. Proc. Soc. Exp. Biol. Med. 1971; 136: 349
   PubMed Web of Science ®Google Scholar
• Huang K. Y., Donahoe R. M., Gordon F. B., Dresler H. R. Enhancement of phagocytosis by interferon-containing preparations. Infect. Immun. 1971; 4: 581
   PubMed Web of Science ®Google Scholar
• Bucknall R. A. Species specificity of interferons: a misnomer?. Nature 1967; 216: 1022
   PubMed Web of Science ®Google Scholar
• Moehring J. M., Stinebring W. R. Order specificity of certain avian interferons. Ann. N.Y. Acad. Sci. 1970; 173: 538
   Google Scholar
• Bodo G., Palese P., Lindner J. Activity of mouse interferon in human cells. Proc. Soc. Exp. Biol. Med. 1971; 137: 1392
   Google Scholar