Abstract
Treatment of Herpesvirus saimiri (HVS)-infected owl monkey cells by limited papain digestion removed the HVS-induced membrane antigen (MA) as determined by membrane immunofluorescence and antibody-dependent lymphocyte cytotoxicity (ADLC). Soluble antigenically active HVSMA was detected by inhibition of ADLC and by the decreased binding of 125I-labeled staphylococcus protein A to HVS-infected cells after absorption of an anti-MA-positive serum with papain extracts. Approximately 38% of the inhibitory activity of the papain extracts was sedimentable at 100,000 X g, indicating that the released MA was heterogeneous in size. Preliminary investigations by gel filtration chromatography identified a major peak of MA with a molecular weight between 20,000 and 50,000.
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- Ablashi D. V., Loeb W. F., Valerio M. G., Adamson R. H., Armstrong G. R., Bennett D. G., Heine U. Malignant lymphoma with lymphocytic leukemia induced in owl monkeys by Herpesvirus saimiri. J Natl Cancer Inst. 1971 Oct;47(4):837–855. [PubMed] [Google Scholar]
- Dölken G., Klein G. A solid-phase radioimmunoassay for Epstein-Barr virus-associated membrane antigen prepared from B95-8 cell culture supernatants. J Natl Cancer Inst. 1977 May;58(5):1239–1245. doi: 10.1093/jnci/58.5.1239. [DOI] [PubMed] [Google Scholar]
- Ernberg I., Klein G., Kourilsky F. M., Silvestre D. Differentiation between early and late membrane antigen on human lymphoblastoid cell lines infected with Epstein-Barr virus. I. Immunofluorescence. J Natl Cancer Inst. 1974 Jul;53(1):61–65. doi: 10.1093/jnci/53.1.61. [DOI] [PubMed] [Google Scholar]
- Glorioso J. C., Smith J. W. Immune interactions with cells infected with herpes simplex virus: antibodies to radioiodinated surface antigens. J Immunol. 1977 Jan;118(1):114–121. [PubMed] [Google Scholar]
- Heine J. W., Roizman B. Proteins specified by herpes simplex virus. IX. Contiguity of host and viral proteins in the plasma membrane of infected cells. J Virol. 1973 May;11(5):810–813. doi: 10.1128/jvi.11.5.810-813.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hunt R. D., Meléndez L. V., King N. W., Gilmore C. E., Daniel M. D., Williamson M. E., Jones T. C. Morphology of a disease with features of malignant lymphoma in marmosets and owl monkeys inoculated with Herpesvirus saimiri. J Natl Cancer Inst. 1970 Feb;44(2):447–465. [PubMed] [Google Scholar]
- Kaaden O. R., Dietzschold B. Alterations of the immunological specificity of plasma membranes from cells infected with Marek's disease and turkey herpes viruses. J Gen Virol. 1974 Oct;25(1):1–10. doi: 10.1099/0022-1317-25-1-1. [DOI] [PubMed] [Google Scholar]
- Klein G., Clifford P., Klein E., Stjernswärd J. Search for tumor-specific immune reactions in Burkitt lymphoma patients by the membrane immunofluorescence reaction. Proc Natl Acad Sci U S A. 1966 Jun;55(6):1628–1635. doi: 10.1073/pnas.55.6.1628. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein G., Pearson G., Nadkarni J. S., Nadkarni J. J., Klein E., Henle G., Henle W., Clifford P. Relation between Epstein-Barr viral and cell membrane immunofluorescence of Burkitt tumor cells. I. Dependence of cell membrane immunofluorescence on presence of EB virus. J Exp Med. 1968 Nov 1;128(5):1011–1020. doi: 10.1084/jem.128.5.1011. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klein G., Pearson G., Rabson A., Ablashi D. V., Falk L., Wolfe L., Dienhardt F., Rabin H. Antibody reactions to herpesvirus saimiri (HVS)-induced early and late antigens (EA and LA) in HVS-infected squirrel, marmoset and owl monkeys. Int J Cancer. 1973 Jul 15;12(1):270–289. doi: 10.1002/ijc.2910120128. [DOI] [PubMed] [Google Scholar]
- Meléndez L. V., Daniel M. D., Hunt R. D., Fraser C. E., Garciá F. G., King N. W., Williamson M. E. Herpesvirus saimiri. V. Further evidence to consider this virus as the etiological agent of a lethal disease in primates which resembles a malignant lymphoma. J Natl Cancer Inst. 1970 May;44(5):1175–1181. [PubMed] [Google Scholar]
- Pearson G. R., Henle G., Henle W. Production of antigens associated with Epstein-Barr virus in experimentally infected lymphoblastoid cell lines. J Natl Cancer Inst. 1971 Jun;46(6):1243–1250. [PubMed] [Google Scholar]
- Pearson G., Ablashi D., Orr T., Rabin H., Armstrong G. Intracellular and membrane immunofluorescence investigations on cells infected with Herpesvirus saimiri. J Natl Cancer Inst. 1972 Nov;49(5):1417–1424. [PubMed] [Google Scholar]
- Prevost J. M., Pearson G. R., Wallen W. C., Rabin H., Qualtiere L. F. Antibody responses to membrane antigens in monkeys infected with Herpesvirus saimiri. Int J Cancer. 1976 Nov 15;18(5):679–686. doi: 10.1002/ijc.2910180517. [DOI] [PubMed] [Google Scholar]
- Prevost J., Orr T. W., Pearson G. R. Augmentation of lymphocyte cytotoxicity by antibody to herpesvirus saimiri associated antigens. Proc Natl Acad Sci U S A. 1975 May;72(5):1671–1675. doi: 10.1073/pnas.72.5.1671. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Silvestre D., Kourilsky F. M., Klein G., Yata Y., Neauport-Sautes C., Levy J. P. Relationship between the EBV-associated membrane antigen on Burkitt lymphoma cells and the viral envelope, demonstrated by immunoferritin labelling. Int J Cancer. 1971 Sep 15;8(2):222–233. doi: 10.1002/ijc.2910080206. [DOI] [PubMed] [Google Scholar]
- Sparks F. C., Ting C. C., Hammond W. G., Herberman R. B. An isotopic antiglobulin technique for measuring antibodies to cell-surface antigens. J Immunol. 1969 Apr;102(4):842–847. [PubMed] [Google Scholar]
- Spear P. G., Kellejmroian B. Proteins spcified by herpes simplex virus. II. Viral glycoprotins associated with cellular membranes. J Virol. 1970 Feb;5(2):123–131. doi: 10.1128/jvi.5.2.123-131.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WATKINS J. F. ADSORPTION OF SENSITIZED SHEEP ERYTHROCYTES TO HELA CELLS INFECTED WITH HERPES SIMPLEX VIRUS. Nature. 1964 Jun 27;202:1364–1365. doi: 10.1038/2021364a0. [DOI] [PubMed] [Google Scholar]
- Ziegler H. K., Henney C. S. Antibody-dependent cytolytically active human leukocytes: an analysis of inactivation following in vitro interaction with antibody-coated target cells. J Immunol. 1975 Dec;115(6):1500–1504. [PubMed] [Google Scholar]

