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. 1981 Oct;44(4):514–521. doi: 10.1038/bjc.1981.220

Canine transmissible venereal sarcoma: distribution of T and B lymphocytes in blood, draining lymph nodes and tumours at different stages of growth.

J P Chandler, T J Yang
PMCID: PMC2010818  PMID: 6975111

Abstract

The levels of T, B and null lymphocytes in the peripheral blood, draining lymph nodes, and tumour masses at different growth stages in dogs transplanted with canine transmissible venereal sarcoma (CTVS) were determined by immunofluorescence techniques. The tumours were classified at excision into "progressor", "steady state", and "regressor" stages of growth. The percentage of B cells in the lymphocytes infiltrating into the progressively growing tumours (n = 10, 37.3 +/- 7.4%) was significantly higher (P less than 0.025) than that in regressing tumours (n = 21, 26.1 +/- 1.9%). In contrast, the percentage of T cells in the lymphocytes infiltrating into the regressing tumours (n = 21, 61.2 +/- 2.6%) was significantly higher (P less than 0.005) than that in the progressively growing tumours (n = 10, 34.0 +/- 5.1%). The tumours at the steady-state growth stage (n = 9) had 50.8 +/- 5.7% infiltrating T-cells, which was significantly higher (P less than 0.005) than the progressors and lower (P less than 0.005) than the regressors. The percentage of null cells of progressors (n = 10, 26.0 +/- 6.9%) was significantly (P less than 0.025) higher than in regressors (n = 21, 13.5 +/- 2.9%). The draining lymph nodes of progressor dogs (n = 5) had significantly fewer (P less than 0.025) B cells (8.2 +/- 2.3%) than in normal (n = 5, 16.1 +/- 3.1%), regressors (n = 12, 19.1 +/- 1.7%) and steady-state dogs (n = 5, 15.8 +/- 2.6%). Although there was slight lymphopenia and fluctuation of null cells, no significant differences in T- and B-lymphocyte levels were noted in the peripheral blood of the tumour dogs (n = 44) studied.

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Selected References

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  1. Alexander E. L., Sanders S. K. F(ab')2 reagents are not required if goat, rather than rabbit, antibodies are used to detect human surface immunoglobulin. J Immunol. 1977 Sep;119(3):1084–1088. [PubMed] [Google Scholar]
  2. Blazer B. A., Heppner G. H. In situ lymphoid cells of mouse mammary tumors. II. The characterization of lymphoid cells separated from mouse mammary tumors. J Immunol. 1978 Jun;120(6):1881–1886. [PubMed] [Google Scholar]
  3. Chandler J. P., Yang T. J. Identification of canine lymphocyte populations by immunofluorescence surface marker analysis. Int Arch Allergy Appl Immunol. 1981;65(1):62–68. doi: 10.1159/000232738. [DOI] [PubMed] [Google Scholar]
  4. Cohen D. In vitro cell-mediated cytotoxicity and antibody-dependent cellular cytotoxicity to the transmissible venereal tumor of the dog. J Natl Cancer Inst. 1980 Feb;64(2):317–321. doi: 10.1093/jnci/64.2.317. [DOI] [PubMed] [Google Scholar]
  5. Cohen D. The biological behaviour of the transmissible venereal tumour in immunosuppressed dogs. Eur J Cancer. 1973 Apr;9(4):253–258. doi: 10.1016/0014-2964(73)90090-x. [DOI] [PubMed] [Google Scholar]
  6. Domagala W., Emeson E. E., Koss L. G. Distribution of T-lymphocytes and B-lymphocytes in peripheral blood and effusions of patients with cancer. J Natl Cancer Inst. 1978 Aug;61(2):295–300. [PubMed] [Google Scholar]
  7. Edelson R. L., Hearing V. J., Dellon A. L., Frank M., Edelson E. K., Green I. Differentiation between B cells, T cells, and histiocytes in melanocytic lesions: primary and metastatic melanoma and halo and giant pigmented nevi. Clin Immunol Immunopathol. 1975 Nov;4(4):557–568. doi: 10.1016/0090-1229(75)90097-5. [DOI] [PubMed] [Google Scholar]
  8. Emeson E. E. Migratory behavior of lymphocytes with specific reactivity to alloantigens. II. Selective recruitment to lymphoid cell allografts and their draining lymph nodes. J Exp Med. 1978 Jan 1;147(1):13–24. doi: 10.1084/jem.147.1.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Garnis S., Lala P. K. Surface markers of small lymphocytes appearing in the mouse Ehrlich ascites tumour, host spleen and blood. Immunology. 1978 Mar;34(3):487–499. [PMC free article] [PubMed] [Google Scholar]
  10. Harding M. W., Yang T. J. Canine transmissible venereal sarcoma: leukocyte adherence inhibition (LAI) reactivity of various lymphoid tissues of dogs with tumors at different stages of growth. Int J Cancer. 1981 Mar 15;27(3):349–355. doi: 10.1002/ijc.2910270314. [DOI] [PubMed] [Google Scholar]
  11. Holden H. T., Haskill J. S., Kirchner H., Herberman R. B. Two functionally distinct anti-tumor effector cells isolated from primary murine sarcoma virus-induced tumors. J Immunol. 1976 Aug;117(2):440–446. [PubMed] [Google Scholar]
  12. Klein E., Becker S., Svedmyr E., Jondal M., Vánky F. Tumor infiltrating lymphocytes. Ann N Y Acad Sci. 1976;276:207–216. doi: 10.1111/j.1749-6632.1976.tb41647.x. [DOI] [PubMed] [Google Scholar]
  13. Klobusická M., Kalafut F., Novotná L. Studies on T and B lymphocytes in rats bearing methylcholanthrene-induced tumor. Neoplasma. 1978;25(6):667–677. [PubMed] [Google Scholar]
  14. Konorza G., Sesterhenn K., Krueger G. R., Ablashi D. V. Distribution of T- and B-cells and of immunoglobulin-producing cells in tumor tissue of patients with nasopharyngeal carcinoma. J Cancer Res Clin Oncol. 1979 Feb 19;93(2):195–204. doi: 10.1007/BF00406578. [DOI] [PubMed] [Google Scholar]
  15. Muscoplat C. C., Schoster J. V., Osborne C. A., Johnson D. W. Density gradient separation of lymphocytes, eosinophils, and microfilariae from blood of dogs infected with Dirofilaria immitis. Am J Vet Res. 1977 Dec;38(12):2095–2096. [PubMed] [Google Scholar]
  16. Palker T. J., Yang T. J. Identification and physicochemical characterization of a tumor-associated antigen from canine transmissible venereal sarcoma. J Natl Cancer Inst. 1981 Apr;66(4):779–787. [PubMed] [Google Scholar]
  17. Russell S. W., Gillespie G. Y., Hansen C. B., Cochrane C. G. Inflammatory cells in solid murine neoplasms. II. Cell types found throughout the course of Moloney sarcoma regression or progression. Int J Cancer. 1976 Sep 15;18(3):331–338. doi: 10.1002/ijc.2910180310. [DOI] [PubMed] [Google Scholar]
  18. Santer V., Mastromarino J. H., Lala P. K. Characterization of lymphocyte subsets in spontaneous mouse mammary tumors and host lymphoid organs. Int J Cancer. 1980 Jan 15;25(1):159–168. doi: 10.1002/ijc.2910250122. [DOI] [PubMed] [Google Scholar]
  19. Silverman N. A., Alexander J. C., Jr, Potvin C., Chretien P. B. In vitro lymphocyte reactivity and T cell levels in patients with melanoma: correlations with clinical and pathological stage. Surgery. 1976 Mar;79(3):332–339. [PubMed] [Google Scholar]
  20. Svennevig J. L., Closs O., Harboe M., Svaar H. Characterization of lymphocytes isolated from non-lymphoid human malignant tumours. Scand J Immunol. 1978;7(6):487–493. doi: 10.1111/j.1365-3083.1978.tb00482.x. [DOI] [PubMed] [Google Scholar]
  21. Svennevig J. L., Lövik M., Svaar H. Isolation and characterization of lymphocytes and macrophages from solid, malignant human tumours. Int J Cancer. 1979 May 15;23(5):626–631. doi: 10.1002/ijc.2910230507. [DOI] [PubMed] [Google Scholar]
  22. Thynne G. S., Moertel C. G., Silvers A. Preoperative lymphocyte counts in peripheral blood in patients with colorectal neoplasms: a correlation with tumor type, Dukes' classification, site of primary tumor, and five-year survival rate in 1,000 patients. Dis Colon Rectum. 1979 May-Jun;22(4):221–222. doi: 10.1007/BF02586878. [DOI] [PubMed] [Google Scholar]
  23. Vider M., Maruyama Y., Narvaez R. Significance of the vertebral venous (Batson's) plexus in metastatic spread in colorectal carcinoma. Cancer. 1977 Jul;40(1):67–71. doi: 10.1002/1097-0142(197707)40:1<67::aid-cncr2820400113>3.0.co;2-f. [DOI] [PubMed] [Google Scholar]
  24. Vose B. M., Vánky F., Klein E. Human tumour--lymphocyte interaction in vitro. V. Comparison of the reactivity of tumour-infiltrating, blood and lymph-node lymphocytes with autologous tumour cells. Int J Cancer. 1977 Dec 15;20(6):895–902. doi: 10.1002/ijc.2910200612. [DOI] [PubMed] [Google Scholar]
  25. Wood G. W., Neff J. R. A reevaluation of B-lymphocyte levels in peripheral blood from cancer patients. J Natl Cancer Inst. 1978 Sep;61(3):715–718. [PubMed] [Google Scholar]
  26. Yang T. J., Jones J. B. Canine transmissible venereal sarcoma: transplantation studies in neonatal and adult dogs. J Natl Cancer Inst. 1973 Dec;51(6):1915–1918. doi: 10.1093/jnci/51.6.1915. [DOI] [PubMed] [Google Scholar]
  27. Yang T. J., Roberts R. S., Jones J. B. Quantitative study of lymphoreticular infiltration into canine transmissible venereal sarcoma. Virchows Arch B Cell Pathol. 1976 Apr 29;20(3):197–204. doi: 10.1007/BF02890339. [DOI] [PubMed] [Google Scholar]

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