Abstract
The mechanism of influenza virus (INFV)-induced immunosuppression and the mode of inosiplex action against INFV infection were studied. INFV suppressed both anti-lipopolysaccharide and anti-sheep erythrocyte antibody production in mice. INFV infection caused viral mRNA synthesis and increased total RNA synthesis in lymphocytes, but total mRNA synthesis was decreased. The translational ability of INFV-infected lymphocytes was also suppressed. Thus, INFV seemed to cause suppression of both mRNA synthesis and the translational ability of lymphocytes, resulting in suppression of lymphocyte functions. Inosiplex potentiated antibody production against sheep erythrocytes but not against lipopolysaccharide in normal and INFV-infected mice. Adamantanamine did not produce such a potentiating effect. The lymphocytes obtained from INFV-immunized and inosiplex-treated mice conferred resistance against INFV infection. This resistance was partially inhibited by anti-Thy 1.2 antibody treatment of the lymphocytes. In an adoptive cell transfer system, inosiplex treatment of T-cell donors potentiated antibody production when a non-immunosuppressive carrier (human serum albumin) was used. When an immunosuppressive carrier (INFV) was used, inosiplex treatment of either B-cell donors or T-cell donors increased antibody production. Direct introduction of inosiplex into lymphocytes by a cell fusion technique stimulated anti-sheep erythrocyte antibody production more effectively than the addition of inosiplex to cultures. Inosiplex increased total RNA and total mRNA syntheses in phytohemagglutinin-treated lymphocytes. In INFV-infected lymphocytes, inosiplex decreased syntheses of total RNA, total mRNA, and viral mRNA and restored translational ability. From these results, we concluded that inosiplex penetrates into lymphocytes and suppresses viral RNA synthesis and that it supports lymphocyte functions by promoting RNA synthesis and translational ability, both of which are necessary for hosts.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aviv H., Leder P. Purification of biologically active globin messenger RNA by chromatography on oligothymidylic acid-cellulose. Proc Natl Acad Sci U S A. 1972 Jun;69(6):1408–1412. doi: 10.1073/pnas.69.6.1408. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BARRY R. D. THE EFFECTS OF ACTINOMYCIN D AND ULTRAVIOLET IRRADIATION ON THE PRODUCTION OF FOWL PLAGUE VIRUS. Virology. 1964 Dec;24:563–569. doi: 10.1016/0042-6822(64)90208-9. [DOI] [PubMed] [Google Scholar]
- Cunningham A. J., Szenberg A. Further improvements in the plaque technique for detecting single antibody-forming cells. Immunology. 1968 Apr;14(4):599–600. [PMC free article] [PubMed] [Google Scholar]
- EISEN H. N. PREPARATION OF PURIFIED ANTI-2,4-DINITROPHENYL ANTIBODIES. Methods Med Res. 1964;10:94–102. [PubMed] [Google Scholar]
- Follett E. A., Pringle C. R., Wunner W. H., Skehel J. J. Virus replication in enucleate cells: vesicular stomatitis virus and influenza virus. J Virol. 1974 Feb;13(2):394–399. doi: 10.1128/jvi.13.2.394-399.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gordon P., Brown E. R. The antiviral activity of isoprinosine. Can J Microbiol. 1972 Sep;18(9):1463–1470. doi: 10.1139/m72-224. [DOI] [PubMed] [Google Scholar]
- Gordon P., Ronsen B., Brown E. R. Anti-herpesvirus action of isoprinosine. Antimicrob Agents Chemother. 1974 Feb;5(2):153–160. doi: 10.1128/aac.5.2.153. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hadden J. W., Lopez C., O'Reilly R. J., Hadden E. M. Levamisole and inosiplex: antiviral agents with immunopotentiating action. Ann N Y Acad Sci. 1977 Mar 4;284:139–152. doi: 10.1111/j.1749-6632.1977.tb21945.x. [DOI] [PubMed] [Google Scholar]
- Hamaoka T., Kitagawa M., Matsuoka Y., Yamamura Y. Antibody production in mice. I. The analysis of immunological memory. Immunology. 1969 Jul;17(1):55–69. [PMC free article] [PubMed] [Google Scholar]
- Housman D., Pemberton R., Taber R. Synthesis of and chains of rabbit hemoglobin in a cell-free extract from Krebs II ascites cells. Proc Natl Acad Sci U S A. 1971 Nov;68(11):2716–2719. doi: 10.1073/pnas.68.11.2716. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kato N., Eggers H. J. Inhibition of uncoating of fowl plague virus by l-adamantanamine hydrochloride. Virology. 1969 Apr;37(4):632–641. doi: 10.1016/0042-6822(69)90281-5. [DOI] [PubMed] [Google Scholar]
- Krug R. M. Cytoplasmic and nucleoplasmic viral RNPs in influenza virus-infected MDCK cells. Virology. 1972 Oct;50(1):103–113. doi: 10.1016/0042-6822(72)90350-9. [DOI] [PubMed] [Google Scholar]
- Krug R. M., Morgan M. A., Shatkin A. J. Influenza viral mRNA contains internal N6-methyladenosine and 5'-terminal 7-methylguanosine in cap structures. J Virol. 1976 Oct;20(1):45–53. doi: 10.1128/jvi.20.1.45-53.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lindberg U., Persson T. Isolation of mRNA from KB-cells by affinity chromatography on polyuridylic acid covalently linked to Sepharose. Eur J Biochem. 1972 Dec 4;31(2):246–254. doi: 10.1111/j.1432-1033.1972.tb02527.x. [DOI] [PubMed] [Google Scholar]
- Long W. F., Burke D. C. The effect of infection with fowl plague virus on protein synthesis in chick embryo cells. J Gen Virol. 1970 Jan;6(1):1–14. doi: 10.1099/0022-1317-6-1-1. [DOI] [PubMed] [Google Scholar]
- Notkins A. L., Mergenhagen S. E., Howard R. J. Effect of virus infections on the function of the immune system. Annu Rev Microbiol. 1970;24:525–538. doi: 10.1146/annurev.mi.24.100170.002521. [DOI] [PubMed] [Google Scholar]
- Ohnishi H., Kosuzume H., Inaba H., Okura M., Shimada S., Tajima H., Suzuki Y. [Effects of inosiplex on viral growth and experimental viral infections (author's transl)]. Kansenshogaku Zasshi. 1981 Jul;55(7):490–500. doi: 10.11150/kansenshogakuzasshi1970.55.490. [DOI] [PubMed] [Google Scholar]
- Ohnishi H., Kosuzume H., Inaba H., Okura M., Tajima H., Suzuki Y. [Protective effects of inosiplex in viral infections. Comparison with other immunostimulants (author's transl)]. Kansenshogaku Zasshi. 1981 Aug;55(8):551–557. doi: 10.11150/kansenshogakuzasshi1970.55.551. [DOI] [PubMed] [Google Scholar]
- Ohnishi H., Kosuzume H., Inaba H., Shimada S., Tajima H., Suzuki Y. [Protective effects of inosiplex in viral infections. The activity of inosiplex and its constituents (author's transl)]. Kansenshogaku Zasshi. 1981 Aug;55(8):541–550. doi: 10.11150/kansenshogakuzasshi1970.55.541. [DOI] [PubMed] [Google Scholar]
- Pons M. W. Early RNA synthesis in influenza virus-infected cells. Virology. 1977 Feb;76(2):855–859. doi: 10.1016/0042-6822(77)90265-3. [DOI] [PubMed] [Google Scholar]
- Rittenberg M. B., Pratt K. L. Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen. Proc Soc Exp Biol Med. 1969 Nov;132(2):575–581. doi: 10.3181/00379727-132-34264. [DOI] [PubMed] [Google Scholar]
- Stobo J. D., Rosenthal A. S., Paul W. E. Functional heterogeneity of murine lymphoid cells. I. Responsiveness to and surface binding of concanavalin A and phytohemagglutinin. J Immunol. 1972 Jan;108(1):1–17. [PubMed] [Google Scholar]
- Taylor J. M., Illmensee R., Litwin S., Herring L., Broni B., Krug R. M. Use of specific radioactive probes to study transcription and replication of the influenza virus genome. J Virol. 1977 Feb;21(2):530–540. doi: 10.1128/jvi.21.2.530-540.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wallace D. M., Jagus R., Benzie C. R., Kay J. E. Translational activity of messenger ribonucleic acid isolated from unstimulated and phytohaemagglutinin-activated lymphocytes. Biochem J. 1979 Nov 15;184(2):277–282. doi: 10.1042/bj1840277. [DOI] [PMC free article] [PubMed] [Google Scholar]
- White D. O., Cheyne I. M. Early events in the eclipse phase of influenza and parainfluenza virus infection. Virology. 1966 May;29(1):49–59. doi: 10.1016/0042-6822(66)90195-4. [DOI] [PubMed] [Google Scholar]