Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1973 Feb 28;137(3):751–775. doi: 10.1084/jem.137.3.751

IMMUNOLOGIC REJECTION OF DIETHYLNITROSAMINE-INDUCED HEPATOMAS IN STRAIN 2 GUINEA PIGS

PARTICIPATION OF BASOPHILIC LEUKOCYTES AND MACROPHAGE AGGREGATES

Harold F Dvorak 1, Ann M Dvorak 1, Winthrop H Churchill 1
PMCID: PMC2139377  PMID: 4347597

Abstract

The morphologic events associated with the immunologic rejection by strain 2 guinea pigs of ascites variants of two lines of diethylnitrosamine-induced tumors have been studied by light and electron microscopy. Tumor injection sites in the skin of control animals exhibited clusters of viable, actively mitotic tumor cells along with a modest inflammatory infiltrate composed of lymphocytes, macrophages, neutrophils, and rare basophils. In contrast, similar injections of either tumor line in specifically sensitized guinea pigs elicited typical delayed-type skin reactions associated with tumor cell necrosis and a more extensive inflammatory infiltrate including a selective increase in the number of basophilic leukocytes (12%, line 1, or 23%, line 10, of total inflammatory cells). That basophils may have a role in tumor resistance in vivo is suggested by the close anatomic associations observed between basophils and tumor cells, and by the fact that basophils were the only inflammatory cell to demonstrate a relative increase in frequency in the lesions of sensitized as compared with control animals. Moreover, intraperitoneal injection of line 1 tumor in specifically sensitized animals elicited a striking basophilia within 24 h. Unlike macrophages, basophils did not phagocytose tumor cells but did evidence occasional extrusion of granules and frequently exhibited loss of granule staining density, a change that may be related to release of mediator substances. Electron microscope studies of line 1 tumor rejection in the peritoneal cavities of specifically sensitized guinea pigs demonstrated aggregations of "activated" macrophages, lymphocytes, basophils, and damaged or dead tumor cells. These aggregates, held together by complex interdigitations of macrophage villi, closely resembled those occurring in vitro among peritoneal exudate cells whose migration from capillary tubes was inhibited by migration inhibition factor (MIF). Moreover, cells in these aggregates, as well as macrophages inhibited by MIF in vitro, lacked a normal coating of cell surface material.

Full Text

The Full Text of this article is available as a PDF (2.2 MB).

Selected References

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

  1. BAUER J. A., Jr Genetics of skin transplantation and an estimate of the number of histocompatibility genes in inbred guinea pigs. Ann N Y Acad Sci. 1960 May 31;87:78–92. doi: 10.1111/j.1749-6632.1960.tb23180.x. [DOI] [PubMed] [Google Scholar]
  2. Bast R. C., Jr, Simpson B. A., Dvorak H. F. Heterogeneity of the cellular immune response. II. The role of adjuvant, lymphocyte stimulation in cutaneous basophil hypersensitivity. J Exp Med. 1971 Feb 1;133(2):202–215. doi: 10.1084/jem.133.2.202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Black M. M., Leis H. P., Jr Cellular responses to autologous breast cancer tissue. Correlation with stage and lymphoreticuloendothelial reactive. Cancer. 1971 Aug;28(2):263–273. doi: 10.1002/1097-0142(197108)28:2<263::aid-cncr2820280202>3.0.co;2-a. [DOI] [PubMed] [Google Scholar]
  4. Burnet F. M. The concept of immunological surveillance. Prog Exp Tumor Res. 1970;13:1–27. doi: 10.1159/000386035. [DOI] [PubMed] [Google Scholar]
  5. Churchill W. H., Zbar B., Belli J. A., David J. R. Detection of cellular immunity to tumor antigens of a guinea pig hepatoma by inhibition of macrophage migration. J Natl Cancer Inst. 1972 Feb;48(2):541–549. [PubMed] [Google Scholar]
  6. Dvorak A. M., Dvorak H. F., Karnovsky M. J. Uptake of horseradish peroxidase by guinea pig basophilic leukocytes. Lab Invest. 1972 Jan;26(1):27–39. [PubMed] [Google Scholar]
  7. Dvorak A. M., Hammond M. E., Dvorak H. F., Karnovsky M. J. Loss of cell surface material from peritoneal exudate cells associated with lymphocyte-mediated inhibition of macrophage migration from capillary tubes. Lab Invest. 1972 Dec;27(6):561–574. [PubMed] [Google Scholar]
  8. Dvorak H. F., Dvorak A. M. Basophils, mast cells, and cellular immunity in animals and man. Hum Pathol. 1972 Dec;3(4):454–456. doi: 10.1016/s0046-8177(72)80004-2. [DOI] [PubMed] [Google Scholar]
  9. Dvorak H. F., Dvorak A. M., Simpson B. A., Richerson H. B., Leskowitz S., Karnovsky M. J. Cutaneous basophil hypersensitivity. II. A light and electron microscopic description. J Exp Med. 1970 Sep 1;132(3):558–582. doi: 10.1084/jem.132.3.558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Dvorak H. F., Hirsch M. S. Role of basophilic leukocytes in cellular immunity to vaccinia virus infection. J Immunol. 1971 Dec;107(6):1576–1582. [PubMed] [Google Scholar]
  11. Dvorak H. F., Mihm M. C., Jr Basophilic leukocytes in allergic contact dermatitis. J Exp Med. 1972 Feb 1;135(2):235–254. doi: 10.1084/jem.135.2.235. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Dvorak H. F. Role of the basophilic leukocyte in allograft rejection. J Immunol. 1971 Jan;106(1):279–281. [PubMed] [Google Scholar]
  13. Dvorak H. F., Simpson B. A., Bast R. C., Jr, Leskowitz S. Cutaneous basophil hypersensitivity. 3. Participation of the basophil in hypersensitivity to antigen-antibody complexes, delayed hypersensitivity and contact allergy. Passive transfer. J Immunol. 1971 Jul;107(1):138–148. [PubMed] [Google Scholar]
  14. Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J Cell Biol. 1965 Jul;26(1):263–291. doi: 10.1083/jcb.26.1.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Hellström I., Hellström K. E., Pierce G. E., Yang J. P. Cellular and humoral immunity to different types of human neoplasms. Nature. 1968 Dec 28;220(5174):1352–1354. doi: 10.1038/2201352a0. [DOI] [PubMed] [Google Scholar]
  16. Karnovsky M. J. The ultrastructural basis of capillary permeability studied with peroxidase as a tracer. J Cell Biol. 1967 Oct;35(1):213–236. doi: 10.1083/jcb.35.1.213. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Klein G. Tumor antigens. Annu Rev Microbiol. 1966;20:223–252. doi: 10.1146/annurev.mi.20.100166.001255. [DOI] [PubMed] [Google Scholar]
  18. Kronman B. S., Wepsic H. T., Churchill W. H., Jr, Zbar B., Borsos T., Rapp H. J. Immunotherapy of cancer: an experimental model in syngeneic guinea pigs. Science. 1970 Apr 10;168(3928):257–259. doi: 10.1126/science.168.3928.257. [DOI] [PubMed] [Google Scholar]
  19. Kronman B. S., Wepsic H. T., Churchill W. H., Jr, Zbar B., Borsos T., Rapp H. J. Tumor-specific antigens detected by inhibition of macrophage migration. Science. 1969 Jul 18;165(3890):296–297. doi: 10.1126/science.165.3890.296. [DOI] [PubMed] [Google Scholar]
  20. Lowell F. C. Clinical aspects of eosinophilia in atopic disease. JAMA. 1967 Nov 27;202(9):875–878. [PubMed] [Google Scholar]
  21. Old L. J., Boyse E. A. Antigens of tumors and leukemias induced by viruses. Fed Proc. 1965 Sep-Oct;24(5):1009–1017. [PubMed] [Google Scholar]
  22. ROSENAU W., MOON H. D. Lysis of homologous cells by sensitized lymphocytes in tissue culture. J Natl Cancer Inst. 1961 Aug;27:471–483. [PubMed] [Google Scholar]
  23. Rapp H. J., Churchill W. H., Jr, Kronman B. S., Rolley R. T., Hammond W. G., Borsos T. Antigenicity of a new diethylnitrosamine-induced transplantable guinea pig hepatoma: pathology and formation of ascites variant. J Natl Cancer Inst. 1968 Jul;41(1):1–7. [PubMed] [Google Scholar]
  24. Richerson H. B., Dvorak H. F., Leskowitz S. Cutaneous basophil hypersensitivity. I. A new look at the Jones-Mote reaction, general characteristics. J Exp Med. 1970 Sep 1;132(3):546–557. doi: 10.1084/jem.132.3.546. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Ruddle N. H., Waksman B. H. Cytotoxicity mediated by soluble antigen and lymphocytes in delayed hypersensitivity. 3. Analysis of mechanism. J Exp Med. 1968 Dec 1;128(6):1267–1279. doi: 10.1084/jem.128.6.1267. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Ward P. A., Offen C. D., Montgomery J. R. Chemoattractants of leukocytes, with special reference to lymphocytes. Fed Proc. 1971 Nov-Dec;30(6):1721–1724. [PubMed] [Google Scholar]
  27. Wepsic H. T., Zbar B., Rapp H. J., Borsos T. Systemic transfer of tumor immunity: delayed hypersensitivity and suppression of tumor growth. J Natl Cancer Inst. 1970 Apr;44(4):955–963. [PubMed] [Google Scholar]
  28. Williams T. W., Granger G. A. Lymphocyte in vitro cytotoxicity: correlation of derepression with release of lymphotoxin from human lymphocytes. J Immunol. 1969 Aug;103(2):170–178. [PubMed] [Google Scholar]
  29. Wilson D. B., Billingham R. E. Lymphocytes and transplantation immunity. Adv Immunol. 1967;7:189–273. doi: 10.1016/s0065-2776(08)60129-7. [DOI] [PubMed] [Google Scholar]
  30. Zbar B., Bernstein I. D., Rapp H. J. Suppression of tumor growth at the site of infection with living Bacillus Calmette-Guérin. J Natl Cancer Inst. 1971 Apr;46(4):831–839. [PubMed] [Google Scholar]
  31. Zbar B., Wepsic H. T., Borsos T., Rapp H. J. Tumor-graft rejection in syngeneic guinea pigs: evidence for a two-step mechanism. J Natl Cancer Inst. 1970 Feb;44(2):473–481. [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES