Abstract
A study of the susceptibility of human peripheral blood mononuclear cells to measles virus infection and replication is reported. Resting lymphocytes obtained from adults showed very low levels of infection and virus replication while lymphocytes activated by plant mitogens or allogenic lymphocytes supported mononuclear cells obtained from the umbilical cord of healthy neonates were more susceptible to measles virus infection than those of adults; however, activated cord lymphocytes supported viral replication in the range observed with adult activated lymphocytes. Monocytes obtained from adults were relatively resistant to measles virus infection and replication while neonatal cord blood monocytes supported viral replication to the degree observed with activated lymphocytes. It is hypothesized that infection of acitivated lymphocytes may explain the depression of cell-mediated immunity seen during acute measles virus infection. The significance of the finding that neonatal monocytes are more susceptible to viral infection and replication than adult monocytes is discussed.
Full Text
The Full Text of this article is available as a PDF (799.5 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Allison A. C. On the role of mononuclear phagocytes in immunity against viruses. Prog Med Virol. 1974;18(0):15–31. [PubMed] [Google Scholar]
- BLACK F. L., ROSEN L. Patterns of measles antibodies in residents of Tahiti and their stability in the absence of re-exposure. J Immunol. 1962 Jun;88:725–731. [PubMed] [Google Scholar]
- Brodersen M. P., Burns C. P., Hoak J. C. The separation of human monocytes from blood including biochemical observations. Proc Soc Exp Biol Med. 1973 Dec;144(3):941–944. doi: 10.3181/00379727-144-37716. [DOI] [PubMed] [Google Scholar]
- Brody J. A., Detels R. Subacute sclerosing panencephalitis: a zoonosis following aberrant measles. Lancet. 1970 Sep 5;2(7671):500–501. doi: 10.1016/s0140-6736(70)90116-9. [DOI] [PubMed] [Google Scholar]
- Böyum A. Isolation of mononuclear cells and granulocytes from human blood. Isolation of monuclear cells by one centrifugation, and of granulocytes by combining centrifugation and sedimentation at 1 g. Scand J Clin Lab Invest Suppl. 1968;97:77–89. [PubMed] [Google Scholar]
- Chess L., MacDermott R. P., Schlossman S. F. Immunologic functions of isolated human lymphocyte subpopulations. I. Quantitative isolation of human T and B cells and response to mitogens. J Immunol. 1974 Oct;113(4):1113–1121. [PubMed] [Google Scholar]
- GOOD R. A., ZAK S. J. Disturbances in gamma globulin synthesis as experiments of nature. Pediatrics. 1956 Jul;18(1):109–149. [PubMed] [Google Scholar]
- GRESSER I., CHANY C. Isolation of measles virus from the washed leucocytic fraction of blood. Proc Soc Exp Biol Med. 1963 Jul;113:695–698. doi: 10.3181/00379727-113-28465. [DOI] [PubMed] [Google Scholar]
- Hirsch M. S., Zisman B., Allison A. C. Macrophages and age-dependent resistance to Herpes simplex virus in mice. J Immunol. 1970 May;104(5):1160–1165. [PubMed] [Google Scholar]
- JOHNSON R. T. THE PATHOGENESIS OF HERPES VIRUS ENCEPHALITIS. II. A CELLULAR BASIS FOR THE DEVELOPMENT OF RESISTANCE WITH AGE. J Exp Med. 1964 Sep 1;120:359–374. doi: 10.1084/jem.120.3.359. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jimenez L., Bloom B. R., Blume M. R., Oettgen H. F. On the number and nature of antigen-sensitive lymphocytes in the blood of delayed-hypersensitive human donors. J Exp Med. 1971 Apr 1;133(4):740–751. doi: 10.1084/jem.133.4.740. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kano S., Bloom B. R., Howe M. L. Enumeration of activated thymus-derived lymphocytes by the virus plaque assay. Proc Natl Acad Sci U S A. 1973 Aug;70(8):2299–2303. doi: 10.1073/pnas.70.8.2299. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koller C. A., King G. W., Hurtubise P. E., Sagone A. L., LoBuglio A. F. Characterization of glass adherent human mononuclear cells. J Immunol. 1973 Nov;111(5):1610–1612. [PubMed] [Google Scholar]
- Lohrmann H. P., Novikovs L., Graw R. G., Jr Cellular interactions in the proliferative response of human T and B lymphocytes to phytomitogens and allogeneic lymphocytes. J Exp Med. 1974 Jun 1;139(6):1553–1567. doi: 10.1084/jem.139.6.1553. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MITUS A., ENDERS J. F., EDSALL G., HOLLOWAY A. MEASLES IN CHILDREN WITH MALIGNANCY PROBLEMS AND PREVENTION. Arch Gesamte Virusforsch. 1965;16:331–337. doi: 10.1007/BF01253832. [DOI] [PubMed] [Google Scholar]
- Nahmias A. J., Griffith D., Salsbury C., Yoshida K. Thymic aplasia with lymphopenia, plasma cells, and normal immunoglobulins. Relation to measles virus infection. JAMA. 1967 Sep 4;201(10):729–734. [PubMed] [Google Scholar]
- Norrby E., Vandvik B. Measles and multiple sclerosis. Proc R Soc Med. 1974 Nov;67(11):1129–1132. doi: 10.1177/003591577406701118. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Osunkoya B. O., Adeleye G. I., Adejumo T. A., Salimonu L. S. Studies on leukocyte cultures in measles. II. Detection of measles virus antigen in human leucocytes by immunofluorescence. Arch Gesamte Virusforsch. 1974;44(4):323–329. doi: 10.1007/BF01251013. [DOI] [PubMed] [Google Scholar]
- Osunkoya B. O., Cooke A. R., Ayeni O., Adejumo T. A. Studies on leukocyte cultures in measles. I. Lymphocyte transformation and giant cell formation in leukocyte cultures from clinical cases of measles. Arch Gesamte Virusforsch. 1974;44(4):313–322. [PubMed] [Google Scholar]
- Poste G., Alexander D. J., Reeve P., Hewlett G. Modification of Newcastle disease virus release and cytopathogenicity in cells treated with plant lectins. J Gen Virol. 1974 Jun;23(3):255–270. doi: 10.1099/0022-1317-23-3-255. [DOI] [PubMed] [Google Scholar]
- ROSENBAUM M. J., PHILLIPS I. A., SULLIVAN E. J., EDWARDS E. A., MILLER L. F. A simplified method for virus-tissue culture procedures in microtitration plates. Proc Soc Exp Biol Med. 1963 May;113:224–229. doi: 10.3181/00379727-113-28325. [DOI] [PubMed] [Google Scholar]
- Reeve P., Hewlett G., Watkins H., Alexander D. J., Poste G. Virus-induced cell fusion enhanced by phytohaemagglutinin. Nature. 1974 May 24;249(455):355–356. doi: 10.1038/249355a0. [DOI] [PubMed] [Google Scholar]
- Royston I., Graze P. R., Pitts R. B. Failure of cultured human T-cell lymphoid lines to stimulate in mixed leukocyte culture. J Natl Cancer Inst. 1974 Aug;53(2):361–367. doi: 10.1093/jnci/53.2.361. [DOI] [PubMed] [Google Scholar]
- STARR S., BERKOVICH S. EFFECTS OF MEASLES, GAMMA-GLOBULIN-MODIFIED MEASLES AND VACCINE MEASLES ON THE TUBERCULIN TEST. N Engl J Med. 1964 Feb 20;270:386–391. doi: 10.1056/NEJM196402202700802. [DOI] [PubMed] [Google Scholar]
- Schumacher H. P., Albrecht P., Tauraso N. M. Markers for measles virus. II. Tissue culture properties. Arch Gesamte Virusforsch. 1972;36(3):296–310. doi: 10.1007/BF01249860. [DOI] [PubMed] [Google Scholar]
- Sullivan J. L., Barry D. W., Albrecht P., Lucas S. J. Inhibition of lymphocyte stimulation by measles virus. J Immunol. 1975 May;114(5):1458–1461. [PubMed] [Google Scholar]
- Wheelock E. F., Toy S. T. Participation of lymphocytes in viral infections. Adv Immunol. 1973;16:123–184. doi: 10.1016/s0065-2776(08)60297-7. [DOI] [PubMed] [Google Scholar]
- White R. G., Boyd J. F. The effect of measles on the thymus and other lymphoid tissues. Clin Exp Immunol. 1973 Mar;13(3):343–357. [PMC free article] [PubMed] [Google Scholar]
- Winter G. C., Byles A. B., Yoffey J. M. Blood-lymphocytes in newborn and adult. Lancet. 1965 Nov 6;2(7419):932–933. doi: 10.1016/s0140-6736(65)92905-3. [DOI] [PubMed] [Google Scholar]
- Yamanouchi K., Chino F., Kobune F., Kodama H., Tsuruhara T. Growth of measles virus in the lymphoid tissues of monkeys. J Infect Dis. 1973 Dec;128(6):795–799. doi: 10.1093/infdis/128.6.795. [DOI] [PubMed] [Google Scholar]
