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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1972 Mar;69(3):594–598. doi: 10.1073/pnas.69.3.594

A Factor That Can be Used to Regulate an In Vitro Primary Immune Response

James Watson 1, Marilyn Thoman 1
PMCID: PMC426514  PMID: 4551977

Abstract

A factor has been isolated that supports the stimulation of an immune response against heterologous erythrocyte antigens in mouse spleen cells cultured in a medium that contains deficient serum. The factor is secreted by certain spleen cells that are obtained in permanent culture after leukemia virus infection. The factor permits antigen-sensitive cells derived from bone marrow to mature to antibody-forming cells. This factor can be used in controlling the initiation of a primary immune response in vitro.

Keywords: mice, Rauscher leukemia virus, spleen cells, plaque-forming cells

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Chan E. L., Mishell R. I., Mitchell G. F. Cell interaction in an immune response in vitro: requirement for theta-carrying cells. Science. 1970 Dec 11;170(3963):1215–1217. doi: 10.1126/science.170.3963.1215. [DOI] [PubMed] [Google Scholar]
  2. Claman H. N., Chaperon E. A., Triplett R. F. Immunocompetence of transferred thymus-marrow cell combinations. J Immunol. 1966 Dec;97(6):828–832. [PubMed] [Google Scholar]
  3. Cosenza H., Leserman L. D., Rowley D. A. The third cell type required for the immune response of spleen cells in vitro. J Immunol. 1971 Aug;107(2):414–421. [PubMed] [Google Scholar]
  4. Duc-Nguyen H. Enhancing effect of diethylaminoethyl-dextran on the focus-forming titer of a murine sarcoma virus (Harvey strain). J Virol. 1968 Jun;2(6):643–644. doi: 10.1128/jvi.2.6.643-644.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Friend C., Scher W., Holland J. G., Sato T. Hemoglobin synthesis in murine virus-induced leukemic cells in vitro: stimulation of erythroid differentiation by dimethyl sulfoxide. Proc Natl Acad Sci U S A. 1971 Feb;68(2):378–382. doi: 10.1073/pnas.68.2.378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hartmann K., Dutton R. W., McCarthy M. M., Mishell R. I. Cell components in the immune response. II. Cell attachment separation of immune cells. Cell Immunol. 1970 Jul;1(2):182–189. doi: 10.1016/0008-8749(70)90005-5. [DOI] [PubMed] [Google Scholar]
  7. Haskill J. S., Byrt P., Marbrook J. In vitro and in vivo studies of the immune response to sheep erythrocytes using partially purified cell preparations. J Exp Med. 1970 Jan 1;131(1):57–76. doi: 10.1084/jem.131.1.57. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hoffmann M., Dutton R. W. Immune response restoration with macrophage culture supernatants. Science. 1971 Jun 4;172(3987):1047–1048. doi: 10.1126/science.172.3987.1047. [DOI] [PubMed] [Google Scholar]
  9. Horibata K., Harris A. W. Mouse myelomas and lymphomas in culture. Exp Cell Res. 1970 Apr;60(1):61–77. doi: 10.1016/0014-4827(70)90489-1. [DOI] [PubMed] [Google Scholar]
  10. Kasakura S. Production and specificity of a blastogenic factor in mixed leucocyte cultures from twin sisters. Nature. 1970 Aug 1;227(5257):507–508. doi: 10.1038/227507a0. [DOI] [PubMed] [Google Scholar]
  11. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  12. Mishell R. I., Dutton R. W. Immunization of dissociated spleen cell cultures from normal mice. J Exp Med. 1967 Sep 1;126(3):423–442. doi: 10.1084/jem.126.3.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Mishell R. I., Dutton R. W., Raidt D. J. Cell components in the immune response. I. Gradient separation of immune cells. Cell Immunol. 1970 Jul;1(2):175–181. doi: 10.1016/0008-8749(70)90004-3. [DOI] [PubMed] [Google Scholar]
  14. Mosier D. E. A requirement for two cell types for antibody formation in vitro. Science. 1967 Dec 22;158(3808):1573–1575. doi: 10.1126/science.158.3808.1573. [DOI] [PubMed] [Google Scholar]
  15. Nossal G. J., Cunningham A., Mitchell G. F., Miller J. F. Cell to cell interaction in the immune response. 3. Chromosomal marker analysis of single antibody-forming cells in reconstituted, irradiated, or thymectomized mice. J Exp Med. 1968 Oct 1;128(4):839–853. doi: 10.1084/jem.128.4.839. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Powles R., Balchin L., Currie G. A., Alexander P. Specific autostimulating factor released by lymphocytes. Nature. 1971 May 21;231(5299):161–164. doi: 10.1038/231161a0. [DOI] [PubMed] [Google Scholar]
  17. Watson J. D. The structure and assembly of murine leukemia virus: intracellular viral RNA. Virology. 1971 Sep;45(3):586–597. doi: 10.1016/0042-6822(71)90174-7. [DOI] [PubMed] [Google Scholar]
  18. Watson J., Ralph P., Sarkar S., Cohn M. Leukemia viruses associated with mouse myeloma cells. Proc Natl Acad Sci U S A. 1970 Jun;66(2):344–351. doi: 10.1073/pnas.66.2.344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Wright B. S., Lasfargues J. C. Long-term propagation of the Rauscher murine leukemia virus in tissue culture. J Natl Cancer Inst. 1965 Aug;35(2):319–327. [PubMed] [Google Scholar]

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