Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1987 Nov;70(2):345–353.

Modulation of the defective natural killer activity seen in thalassaemia major with desferrioxamine and alpha-interferon.

A N Akbar 1, P A Fitzgerald-Bocarsly 1, P J Giardina 1, M W Hilgartner 1, R W Grady 1
PMCID: PMC1542076  PMID: 3427826

Abstract

We previously observed that natural killer (NK) activity toward K562 cells is markedly depressed in patients with beta-thalassaemia major. Here we report that these patients also exhibit significantly decreased (P less than 0.005) NK cytotoxicity against human fibroblasts infected with herpes simplex virus-type 1 (HSV-1) and that the amount of alpha-interferon (alpha-IFN) generated during the latter assays is significantly less than normal (P less than 0.005). This decreased production of alpha-IFN may account in part for the decreased NK activity seen in the thalassaemia patients. On the other hand, the cytotoxicity of their mononuclear cells (MNC) toward both K562 cells and HSV-1-infected fibroblasts could be augmented to the same extent as that of normal MNC by preincubation with alpha-IFN suggesting that thalassaemia MNC are capable of responding to this lymphokine despite their reduced ability to produce it. Moreover, preincubation of thalassaemia MNC with desferrioxamine (DFO), an iron-chelating agent, consistently increased the lysis of K562 cells indicating that the transfusion-induced iron overload which these patients experience may also contribute to the defective NK function seen in this disease. We have now found that preincubation of such MNC with DFO has no effect upon production of alpha-IFN when the MNC are cocultured with either HSV-1-infected fibroblasts or K562 cells. Combining DFO and alpha-IFN resulted in an increase in the NK activity of both normal and thalassaemia MNC against the two targets which was greater than that with alpha-IFN alone. In fact, preincubation of thalassaemia cells with this combination increased their NK activity toward K562 targets to that of untreated normal cells. This was true when either unfractionated MNC or NK-enriched fractions were used as effector cells. These results suggest that DFO and alpha-IFN enhance NK activity by different mechanisms, both of which appear to be reversibly impaired in thalassaemia patients.

Full text

PDF
345

Selected References

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

  1. Abruzzo L. V., Rowley D. A. Homeostasis of the antibody response: immunoregulation by NK cells. Science. 1983 Nov 11;222(4624):581–585. doi: 10.1126/science.6685343. [DOI] [PubMed] [Google Scholar]
  2. Akbar A. N., Fitzgerald-Bocarsly P. A., de Sousa M., Giardina P. J., Hilgartner M. W., Grady R. W. Decreased natural killer activity in thalassemia major: a possible consequence of iron overload. J Immunol. 1986 Mar 1;136(5):1635–1640. [PubMed] [Google Scholar]
  3. Akbar A. N., Giardina P. J., Hilgartner M. W., Grady R. W. Immunological abnormalities in thalassaemia major. I. A transfusion-related increase in circulating cytoplasmic immunoglobulin-positive cells. Clin Exp Immunol. 1985 Nov;62(2):397–404. [PMC free article] [PubMed] [Google Scholar]
  4. Arai S., Yamamoto H., Itoh K., Kumagai K. Suppressive effect of human natural killer cells on pokeweed mitogen-induced B cell differentiation. J Immunol. 1983 Aug;131(2):651–657. [PubMed] [Google Scholar]
  5. Baines M. G., Lafleur F. L., Holbein B. E. Involvement of transferrin and transferrin receptors in human natural killer effector:target interaction. Immunol Lett. 1983;7(1):51–55. doi: 10.1016/0165-2478(83)90055-x. [DOI] [PubMed] [Google Scholar]
  6. Bryan C. F., Leech S. H. The immunoregulatory nature of iron. I. Lymphocyte proliferation. Cell Immunol. 1983 Jan;75(1):71–79. doi: 10.1016/0008-8749(83)90306-4. [DOI] [PubMed] [Google Scholar]
  7. Bryan C. F., Nishiya K., Pollack M. S., Dupont B., de Sousa M. Differential inhibition of the MLR by iron: association with HLA phenotype. Immunogenetics. 1981;12(1-2):129–140. doi: 10.1007/BF01561656. [DOI] [PubMed] [Google Scholar]
  8. Fitzgerald P. A., Evans R., Kirkpatrick D., Lopez C. Heterogeneity of human NK cells: comparison of effectors that lyse HSV-1-infected fibroblasts and K562 erythroleukemia targets. J Immunol. 1983 Apr;130(4):1663–1667. [PubMed] [Google Scholar]
  9. Fitzgerald P. A., von Wussow P., Lopez C. Role of interferon in natural kill of HSV-1-infected fibroblasts. J Immunol. 1982 Aug;129(2):819–823. [PubMed] [Google Scholar]
  10. Gascón P., Zoumbos N. C., Young N. S. Immunologic abnormalities in patients receiving multiple blood transfusions. Ann Intern Med. 1984 Feb;100(2):173–177. doi: 10.7326/0003-4819-100-2-173. [DOI] [PubMed] [Google Scholar]
  11. Grady R. W., Akbar A. N., Giardina P. J., Hilgartner M. W., de Sousa M. Disproportionate lymphoid cell subsets in thalassaemia major: the relative contributions of transfusion and splenectomy. Br J Haematol. 1985 Apr;59(4):713–724. doi: 10.1111/j.1365-2141.1985.tb07367.x. [DOI] [PubMed] [Google Scholar]
  12. Graziano J. H., Piomelli S., Hilgartner M., Giardina P., Karpatkin M., Andrew M., LoIacono N., Seaman C. Chelation therapy in beta-thalassemia major. III. The role of splenectomy in achieving iron balance. J Pediatr. 1981 Nov;99(5):695–699. doi: 10.1016/s0022-3476(81)80386-1. [DOI] [PubMed] [Google Scholar]
  13. Kapadia A., de Sousa M., Markenson A. L., Miller D. R., Good R. A., Gupta S. Lymphoid cell sets and serum immunoglobulins in patients with thalassaemia intermedia: relationship to serum iron and splenectomy. Br J Haematol. 1980 Jul;45(3):405–416. doi: 10.1111/j.1365-2141.1980.tb07161.x. [DOI] [PubMed] [Google Scholar]
  14. Kaplan J., Sarnaik S., Gitlin J., Lusher J. Diminished helper/suppressor lymphocyte ratios and natural killer activity in recipients of repeated blood transfusions. Blood. 1984 Jul;64(1):308–310. [PubMed] [Google Scholar]
  15. Lopez C., Kirkpatrick D., Read S. E., Fitzgerald P. A., Pitt J., Pahwa S., Ching C. Y., Smithwick E. M. Correlation between low natural killing of fibroblasts infected with herpes simplex virus type 1 and susceptibility to herpesvirus infections. J Infect Dis. 1983 Jun;147(6):1030–1035. doi: 10.1093/infdis/147.6.1030. [DOI] [PubMed] [Google Scholar]
  16. Matzner Y., Hershko C., Polliack A., Konijn A. M., Izak G. Suppressive effect of ferritin on in vitro lymphocyte function. Br J Haematol. 1979 Jul;42(3):345–353. doi: 10.1111/j.1365-2141.1979.tb01142.x. [DOI] [PubMed] [Google Scholar]
  17. Messina C., Kirkpatrick D., Fitzgerald P. A., O'Reilly R. J., Siegal F. P., Cunningham-Rundles C., Blaese M., Oleske J., Pahwa S., Lopez C. Natural killer cell function and interferon generation in patients with primary immunodeficiencies. Clin Immunol Immunopathol. 1986 Jun;39(3):394–404. doi: 10.1016/0090-1229(86)90167-4. [DOI] [PubMed] [Google Scholar]
  18. Modell B. Total management of thalassaemia major. Arch Dis Child. 1977 Jun;52(6):489–500. doi: 10.1136/adc.52.6.489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Nishiya K., Horwitz D. A. Contrasting effects of lactoferrin on human lymphocyte and monocyte natural killer activity and antibody-dependent cell-mediated cytotoxicity. J Immunol. 1982 Dec;129(6):2519–2523. [PubMed] [Google Scholar]
  20. Pelton B. K., Denman A. M. Immunoregulatory effects of interferon-alpha. I. Interferon-alpha inhibits in vitro antibody synthesis by normal human lymphocytes. Clin Exp Immunol. 1985 Feb;59(2):398–404. [PMC free article] [PubMed] [Google Scholar]
  21. Rönnblom L., Ramstedt U., Alm G. V. Properties of human natural interferon-producing cells stimulated by tumor cell lines. Eur J Immunol. 1983 Jun;13(6):471–476. doi: 10.1002/eji.1830130608. [DOI] [PubMed] [Google Scholar]
  22. Steinhauer E. H., Doyle A. T., Kadish A. S. Human natural killer cytotoxic factor (NKCF): role of IFN-alpha. J Immunol. 1985 Jul;135(1):294–299. [PubMed] [Google Scholar]
  23. Tovo P. A., Miniero R., Barbera C., Sacchetti L., Saitta M. Serum immunoglobulins in homozygous beta-thalassemia. Acta Haematol. 1981;65(1):21–25. doi: 10.1159/000207144. [DOI] [PubMed] [Google Scholar]
  24. Trinchieri G., Santoli D., Dee R. R., Knowles B. B. Anti-viral activity induced by culturing lymphocytes with tumor-derived or virus-transformed cells. Identification of the anti-viral activity as interferon and characterization of the human effector lymphocyte subpopulation. J Exp Med. 1978 May 1;147(5):1299–1313. doi: 10.1084/jem.147.5.1299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Wasi C., Wasi P., Thongcharoen P. Serum-immunoglobulin levels in thalassaemia and the effects of splenectomy. Lancet. 1971 Jul 31;2(7718):237–239. doi: 10.1016/s0140-6736(71)92573-6. [DOI] [PubMed] [Google Scholar]

Articles from Clinical and Experimental Immunology are provided here courtesy of British Society for Immunology

RESOURCES