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. 1984 Oct;20(4):696–700. doi: 10.1128/jcm.20.4.696-700.1984

Use of bone marrow fibroblasts to prepare targets for an HLA restricted-cytotoxicity assay system.

R A Bowden, L McGavren, A R Hayward, M J Levin
PMCID: PMC271414  PMID: 6490855

Abstract

Methods are described for obtaining and growing fibroblasts from bone marrow for use as virus-infected targets. Fibroblasts obtained at the time of routine marrow examination were maintained through 12 to 18 passages as confluent monolayers. Bone marrow fibroblasts could be infected with varicella-zoster virus, and these infected cells were suitable targets for a 51Cr-release cytotoxicity assay. Since these virus-infected cells retain their HLA-A and -B antigens, they are readily available to study the immune cells which mediate virus-specific cytotoxicity.

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Selected References

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  1. Arvin A. M., Pollard R. B., Rasmussen L. E., Merigan T. C. Selective impairment of lymphocyte reactivity to varicella-zoster virus antigen among untreated patients with lymphoma. J Infect Dis. 1978 May;137(5):531–540. doi: 10.1093/infdis/137.5.531. [DOI] [PubMed] [Google Scholar]
  2. Burke B. L., Steele R. W., Beard O. W., Wood J. S., Cain T. D., Marmer D. J. Immune responses to varicella-zoster in the aged. Arch Intern Med. 1982 Feb;142(2):291–293. [PubMed] [Google Scholar]
  3. Castro-Malaspina H., Gay R. E., Resnick G., Kapoor N., Meyers P., Chiarieri D., McKenzie S., Broxmeyer H. E., Moore M. A. Characterization of human bone marrow fibroblast colony-forming cells (CFU-F) and their progeny. Blood. 1980 Aug;56(2):289–301. [PubMed] [Google Scholar]
  4. Dolin R., Reichman R. C., Mazur M. H., Whitley R. J. NIH conference. Herpes zoster-varicella infections in immunosuppressed patients. Ann Intern Med. 1978 Sep;89(3):375–388. doi: 10.7326/0003-4819-89-3-375. [DOI] [PubMed] [Google Scholar]
  5. Feldman S., Hughes W. T., Daniel C. B. Varicella in children with cancer: Seventy-seven cases. Pediatrics. 1975 Sep;56(3):388–397. [PubMed] [Google Scholar]
  6. Feldman S., Hughes W. T., Kim H. Y. Herpes zoster in children with cancer. Am J Dis Child. 1973 Aug;126(2):178–184. doi: 10.1001/archpedi.1973.02110190156009. [DOI] [PubMed] [Google Scholar]
  7. Gershon A. A., Steinberg S. P. Cell-mediated immunity to varicella-zoster virus measured by virus inactivation: mechanism and blocking of the reaction by specific antibody. Infect Immun. 1979 Jul;25(1):164–169. doi: 10.1128/iai.25.1.164-169.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gershon A. A., Steinberg S., Smith M. Cell-mediated immunity to varicella-zoster virus demonstrated by viral inactivation with human leukocytes. Infect Immun. 1976 Jun;13(6):1549–1553. doi: 10.1128/iai.13.6.1549-1553.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gordon M. Y., Gordon-Smith E. C. Bone marrow fibroblastoid colony-forming cells (F-CFC) in aplastic anaemia: colony growth and stimulation of granulocyte-macrophage colony-forming cells (GM-CFC). Br J Haematol. 1981 Nov;49(3):465–477. doi: 10.1111/j.1365-2141.1981.tb07250.x. [DOI] [PubMed] [Google Scholar]
  10. Hayes F. A., Feldman S. Cell-mediated immunity to varicella zoster virus in children being treated for cancer. Cancer. 1978 Jul;42(1):159–163. doi: 10.1002/1097-0142(197807)42:1<159::aid-cncr2820420126>3.0.co;2-e. [DOI] [PubMed] [Google Scholar]
  11. Herberman R. R., Ortaldo J. R., Bonnard G. D. Augmentation by interferon of human natural and antibody-dependent cell-mediated cytotoxicity. Nature. 1979 Jan 18;277(5693):221–223. doi: 10.1038/277221a0. [DOI] [PubMed] [Google Scholar]
  12. Kumagai T., Chiba Y., Wataya Y., Hanazono H., Chiba S., Nakao T. Development and characteristics of the cellular immune response to infection with varicella-zoster virus. J Infect Dis. 1980 Jan;141(1):7–13. doi: 10.1093/infdis/141.1.7. [DOI] [PubMed] [Google Scholar]
  13. Mage M. G., McHugh L. L., Rothstein T. L. Mouse lymphocytes with and without surface immunoglobulin: preparative scale separation in polystyrene tissue culture dishes coated with specifically purified anti-immunoglobulin. J Immunol Methods. 1977;15(1):47–56. doi: 10.1016/0022-1759(77)90016-3. [DOI] [PubMed] [Google Scholar]
  14. Nabholz M., MacDonald H. R. Cytolytic T lymphocytes. Annu Rev Immunol. 1983;1:273–306. doi: 10.1146/annurev.iy.01.040183.001421. [DOI] [PubMed] [Google Scholar]
  15. Nagao T., Komatsuda M., Yamauchi K., Arimori S. Fibroblast colonies in monolayer cultures of human bone marrow. J Cell Physiol. 1981 Aug;108(2):155–161. doi: 10.1002/jcp.1041080206. [DOI] [PubMed] [Google Scholar]
  16. Patel P. A., Yoonessi S., O'Malley J., Freeman A., Gershon A., Ogra P. L. Cell-mediated immunity to varicella-zoster virus infection in subjects with lymphoma or leukemia. J Pediatr. 1979 Feb;94(2):223–230. doi: 10.1016/s0022-3476(79)80828-8. [DOI] [PubMed] [Google Scholar]
  17. Quinnan G. V., Jr, Kirmani N., Esber E., Saral R., Manischewitz J. F., Rogers J. L., Rook A. H., Santos G. W., Burns W. H. HLA-restricted cytotoxic T lymphocyte and nonthymic cytotoxic lymphocyte responses to cytomegalovirus infection of bone marrow transplant recipients. J Immunol. 1981 May;126(5):2036–2041. [PubMed] [Google Scholar]
  18. Quinnan G. V., Jr, Kirmani N., Rook A. H., Manischewitz J. F., Jackson L., Moreschi G., Santos G. W., Saral R., Burns W. H. Cytotoxic t cells in cytomegalovirus infection: HLA-restricted T-lymphocyte and non-T-lymphocyte cytotoxic responses correlate with recovery from cytomegalovirus infection in bone-marrow-transplant recipients. N Engl J Med. 1982 Jul 1;307(1):7–13. doi: 10.1056/NEJM198207013070102. [DOI] [PubMed] [Google Scholar]
  19. Reinherz E. L., Hussey R. E., Schlossman S. F. A monoclonal antibody blocking human T cell function. Eur J Immunol. 1980 Oct;10(10):758–762. doi: 10.1002/eji.1830101006. [DOI] [PubMed] [Google Scholar]
  20. Schimpff S., Serpick A., Stoler B., Rumack B., Mellin H., Joseph J. M., Block J. Varicella-Zoster infection in patients with cancer. Ann Intern Med. 1972 Feb;76(2):241–254. doi: 10.7326/0003-4819-76-2-241. [DOI] [PubMed] [Google Scholar]
  21. Seabright M. A rapid banding technique for human chromosomes. Lancet. 1971 Oct 30;2(7731):971–972. doi: 10.1016/s0140-6736(71)90287-x. [DOI] [PubMed] [Google Scholar]
  22. Slovin S. F., Schooley R. T., Thorley-Lawson D. A. Analysis of cellular immune response to EBV by using cloned T cell lines. J Immunol. 1983 May;130(5):2127–2132. [PubMed] [Google Scholar]
  23. Steele R. W., Hensen S. A., Vincent M. M., Fuccillo D. A., Bellanti J. A. A 51 Cr microassay technique for cell-mediated immunity to viruses. J Immunol. 1973 Jun;110(6):1502–1510. [PubMed] [Google Scholar]
  24. Steele R. W., Keeney R. E., Brown J., 3rd, Young E. J. Cellular immune responses to herpesviruses during treatment with adenine arabinoside. J Infect Dis. 1977 Apr;135(4):593–599. doi: 10.1093/infdis/135.4.593. [DOI] [PubMed] [Google Scholar]
  25. Steele R. W. Transfer factor and cellular reactivity to varicella-zoster antigen in childhood leukemia. Cell Immunol. 1980 Mar 15;50(2):282–289. doi: 10.1016/0008-8749(80)90283-x. [DOI] [PubMed] [Google Scholar]
  26. Yasukawa M., Shiroguchi T., Kobayashi Y. HLA-restricted T lymphocyte-mediated cytotoxicity against herpes simplex virus-infected cells in humans. Infect Immun. 1983 Apr;40(1):190–197. doi: 10.1128/iai.40.1.190-197.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Yu R. L., Aronson M. M., Nichols W. W. High-resolution bands in human fibroblast chromosomes induced by actinomycin D. Cytogenet Cell Genet. 1981;31(2):111–114. doi: 10.1159/000131634. [DOI] [PubMed] [Google Scholar]
  28. Zaia J. A., Oxman M. N. Antibody to varicella-zoster virus-induced membrane antigen: immunofluorescence assay using monodisperse glutaraldehyde-fixed target cells. J Infect Dis. 1977 Oct;136(4):519–530. doi: 10.1093/infdis/136.4.519. [DOI] [PubMed] [Google Scholar]

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