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. 1973 Mar;27(3):203–211. doi: 10.1038/bjc.1973.25

Immunological Studies in Acute Myeloid Leukaemia: PHA Responsiveness and Serum Inhibitory Factors

J S Walker, D Davis, P Davies, C B Freeman, R Harris
PMCID: PMC2008775  PMID: 4511988

Abstract

Sera from 16 of 20 patients with AML at some stage of the disease inhibited the in vitro PHA transformation of normal lymphocytes assessed by measuring the rate of DNA synthesis after 67-70 hours; 42% of pretreatment sera were inhibitory. Inhibitory activity was overcome at PHA concentrations 2-3 times greater than the concentration which allowed maximum discrimination between NHS and leukaemia sera.

PHA transformation of washed lymphocytes obtained from AML patients before treatment and when receiving induction or consolidation (cytoreductive) chemotherapy was reduced only when cultures contained a high proportion of primitive cells. Even in primitive cell contaminated cultures significant responses to PHA could be measured if conditions were modified to prevent increasing acidity.

Reports of reduced in vitro immunological reactions in pretreatment and poor prognosis patients may therefore be due to the presence of primitive cells in culture, and in treated patients to the failure of chemotherapy to reduce the circulating primitive cell count. Serum inhibitory factors may have a significant immunosuppressive effect in vivo, but the accurate assessment of the role of immune mechanisms in AML should attempt the measurement of specific immunity.

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Selected References

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

  1. Astaldi G., Massimo L., Airo R., Mori P. G. Phytohaemagglutinin and lymphocytes from acute lymphocytic leukaemia. Lancet. 1966 Jun 4;1(7449):1265–1266. doi: 10.1016/s0140-6736(66)90279-0. [DOI] [PubMed] [Google Scholar]
  2. Ayoub J., Kasakura S. In vitro response of foetal lymphocytes to PHA, and a factor plasma which suppresses the PHA response of adult lymphocytes. Clin Exp Immunol. 1971 Mar;8(3):427–434. [PMC free article] [PubMed] [Google Scholar]
  3. Bardare M., Accorsi A., Apollonio T., Careddu P. Blastigenesi linfocitaria in vitro da PHA in bambini affetti da leucemia acuta. Minerva Pediatr. 1969 Jun 19;21(23):1019–1024. [PubMed] [Google Scholar]
  4. Cooperband S. R., Green J. A., Kennedy M. A., Grant M. M. Dissociation and inhibition of the stimulatory effect of phytohaemagglutinin on protein and DNA synthesis in human lymphocyte cultures. Nature. 1967 Jun 17;214(5094):1240–1241. doi: 10.1038/2141240a0. [DOI] [PubMed] [Google Scholar]
  5. Coulson A. S., Chalmers D. G. Response of human blood lymphocytes to tuberculin PPD in tissue culture. Immunology. 1967 Apr;12(4):417–429. [PMC free article] [PubMed] [Google Scholar]
  6. Craig A. W., Garrett J. V., Jackson S. M. Quantitation of lymphocyte transformation using radioactive iododeoxyuridine. J Clin Pathol. 1969 Sep;22(5):558–559. doi: 10.1136/jcp.22.5.558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dupuy J. M., Kourilsky F. M., Fradelizzi D., Feingold N., Jacquillat C., Bernard J., Dausset J. Depression of immunologic reactivity of patients with acute leukemia. Cancer. 1971 Feb;27(2):323–331. doi: 10.1002/1097-0142(197102)27:2<323::aid-cncr2820270212>3.0.co;2-m. [DOI] [PubMed] [Google Scholar]
  8. Fitzgerald M. G. The establishment of a normal human population dose-response curve for lymphocytes cultured with PHA (phytohaemagglutinin). Clin Exp Immunol. 1971 Mar;8(3):421–425. [PMC free article] [PubMed] [Google Scholar]
  9. Fridman W. H., Kourilsky F. M. Stimulation of lymphocytes by autologous leukaemic cells in acute leukaemia. Nature. 1969 Oct 18;224(5216):277–279. doi: 10.1038/224277a0. [DOI] [PubMed] [Google Scholar]
  10. Harris R. Leukaemia antigens and immunity in man. Nature. 1973 Jan 12;241(5385):95–100. doi: 10.1038/241095a0. [DOI] [PubMed] [Google Scholar]
  11. Hersh E. M., Whitecar J. P., Jr, McCredie K. B., Bodey G. P., Sr, Freireich E. J. Chemotherapy, immunocompetence, immunosuppression and prognosis in acute leukemia. N Engl J Med. 1971 Nov;285(22):1211–1216. doi: 10.1056/NEJM197111252852201. [DOI] [PubMed] [Google Scholar]
  12. Hsu C. C., Leevy C. M. Inhibition of PHA-stimulated lymphocyte transformation by plasma from patients with advanced alcoholic cirrhosis. Clin Exp Immunol. 1971 May;8(5):749–760. [PMC free article] [PubMed] [Google Scholar]
  13. Jones L. H., Hardisty R. M., Wells D. G., Kay H. E. Lymphocyte transformation in patients with acute lymphoblastic leukaemia. Br Med J. 1971 Nov 6;4(5783):329–330. doi: 10.1136/bmj.4.5783.329. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Knowles M., Hughes D., Caspary E. A., Field E. J. Lymphocyte transformation in multiple sclerosis. Inhibition of unstimulated thymidine uptake by a serum factor. Lancet. 1968 Dec 7;2(7580):1207–1209. doi: 10.1016/s0140-6736(68)91691-7. [DOI] [PubMed] [Google Scholar]
  15. Levene G. M., Turk J. L., Wright D. J., Grimble A. G. Reduced lymphocyte transformation due to a plasma factor in patients with active syphilis. Lancet. 1969 Aug 2;2(7614):246–247. doi: 10.1016/s0140-6736(69)90010-5. [DOI] [PubMed] [Google Scholar]
  16. McFarlin D. E., Oppenheim J. J. Impaired lymphocyte transformation in ataxia-telangiectasia in part due to a plasma inhibitory factor. J Immunol. 1969 Dec;103(6):1212–1222. [PubMed] [Google Scholar]
  17. Silk M. R. The effect of uremic plasma on lymphocyte transformation. Invest Urol. 1967 Sep;5(2):195–199. [PubMed] [Google Scholar]
  18. Silk M. Effect of plasma from patients with carcinoma on in vitro lymphocyte transformation. Cancer. 1967 Dec;20(12):2088–2089. doi: 10.1002/1097-0142(196712)20:12<2088::aid-cncr2820201205>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]
  19. Trubowitz S., Masek B., Del Rosario A. Lymphocyte response to phytohemagglutinin in Hodgkin's disease, lymphatic leukemia and lymphosarcoma. Cancer. 1966 Dec;19(12):2019–2023. doi: 10.1002/1097-0142(196612)19:12<2019::aid-cncr2820191228>3.0.co;2-h. [DOI] [PubMed] [Google Scholar]
  20. Walker J. S., Freeman C. B., Harris R. Lymphocyte reactivity in pregnancy. Br Med J. 1972 Aug 19;3(5824):469–469. doi: 10.1136/bmj.3.5824.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Winter G. C., McCarthy C. F., Read A. E., Yoffey J. M. Development of macrophages in phytohaemagglutinin cultures of blood from patients with idiopathic steatorrhoea and with cirrhosis. Br J Exp Pathol. 1967 Feb;48(1):66–80. [PMC free article] [PubMed] [Google Scholar]

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