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. 1974 Nov;18(3):295–301.

Impaired responsiveness of lymphocytes in patients with systemic lupus erythematosus

Nicole Suciu-Foca, J A Buda, Traute Thiem, K Reemtsma
PMCID: PMC1537988  PMID: 4283364

Abstract

Cellular immune responsiveness, as measured by lymphocyte transformation in one-way mixed leucocyte cultures (MLC) and in phytohaemagglutinin (PHA) stimulated cultures was evaluated in forty patients with systemic lupus erythematosus (SLE) and in seventy-four normal controls. The effect produced by sera from these subjects on in vitro lymphocyte reactivity was tested on autologous cells and on homologous responding cells from a constant panel of ten healthy volunteers.

The reactivity of lymphocytes from SLE patients to PHA and to a battery of allogeneic cells was significantly lower than that of normal controls.

Sera from some SLE patients inhibited the MLC reactions, while in other cases a distinct stimulatory effect was found.

It is suggested that virus-induced modifications of normal histocompatibility antigens cause the appearance of blocking antibody that might bind to the surface of T lymphocytes, impairing their function.

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Selected References

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

  1. Allison A. C., Denman A. M., Barnes R. D. Cooperating and controlling functions of thymus-derived lymphocytes in relation to autoimmunity. Lancet. 1971 Jul 17;2(7716):135–140. doi: 10.1016/s0140-6736(71)92306-3. [DOI] [PubMed] [Google Scholar]
  2. Astorga G. P., Williams R. C., Jr Altered reactivity in mixed lymphocyte culture of lymphocytes from patients with rheumatoid arthritis. Arthritis Rheum. 1969 Dec;12(6):547–554. doi: 10.1002/art.1780120602. [DOI] [PubMed] [Google Scholar]
  3. Buckley R. H., Schiff R. I., Amos D. B. Blocking of autologous and homologous leukocyte responses by human alloimmune plasmas: a possible in vitro correlate of enhancement. J Immunol. 1972 Jan;108(1):34–44. [PubMed] [Google Scholar]
  4. Ceppellini R., Bonnard G. D., Coppo F., Miggiano V. C., Pospisil M., Curtoni E. S., Pellegrino M. Transplantation antigens: introductory symposium. Mixed leukocyte cultures and HL-A antigens. I. Reactivity of young fetuses, newborns and mothers at delivery. Transplant Proc. 1971 Mar;3(1):58–63. [PubMed] [Google Scholar]
  5. Feldman J. D. Immunological enhancement: a study of blocking antibodies. Adv Immunol. 1972;15:167–214. doi: 10.1016/s0065-2776(08)60685-9. [DOI] [PubMed] [Google Scholar]
  6. Gatti R. A., Yunis E. J., Good R. A. Characterization of a serum inhibitor of MLC reactions. Clin Exp Immunol. 1973 Mar;13(3):427–437. [PMC free article] [PubMed] [Google Scholar]
  7. Hattler B. G., Jr, Karesh C., Miller J. Inhibition of the mixed lymphocyte culture response by antibody following successful human renal transplantation. Tissue Antigens. 1971;1(6):270–275. doi: 10.1111/j.1399-0039.1971.tb00105.x. [DOI] [PubMed] [Google Scholar]
  8. Hedberg H., Källén B., Löw B., Nilsson O. Impaired mixed leucocyte reaction in some different diseases, notably multiple sclerosis and various arthritides. Clin Exp Immunol. 1971 Aug;9(2):201–207. [PMC free article] [PubMed] [Google Scholar]
  9. Klippel J. H., Grimley P. M., Decker J. L. Lymphocyte inclusions in newborns of mothers with systemic lupus erythematosus. N Engl J Med. 1974 Jan 10;290(2):96–97. doi: 10.1056/NEJM197401102900208. [DOI] [PubMed] [Google Scholar]
  10. Lueker R. D., Williams R. C., Jr Decreased reactivity of lymphocytes in mixed-leukocyte culture from patients with rheumatic fever. Circulation. 1972 Oct;46(4):655–660. doi: 10.1161/01.cir.46.4.655. [DOI] [PubMed] [Google Scholar]
  11. Messner R. P., Lindström F. D., Williams R. C., Jr Peripheral blood lymphocyte cell surface markers during the course of systemic lupus erythematosus. J Clin Invest. 1973 Dec;52(12):3046–3056. doi: 10.1172/JCI107503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. SELL S., GELL P. G. STUDIES ON RABBIT LYMPHOCYTES IN VITRO. I. STIMULATION OF BLAST TRANSFORMATION WITH AN ANTIALLOTYPE SERUM. J Exp Med. 1965 Aug 1;122:423–440. doi: 10.1084/jem.122.2.423. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Sengar D. P., Opelz G., Terasaki P. I. Outcome of kidney transplants and suppression of mixed leukocyte culture by plasma. Transplant Proc. 1973 Mar;5(1):641–647. [PubMed] [Google Scholar]
  14. Suciu-Foca N., Buda J., McManus J., Thiem T., Reemtsma K. Impaired responsiveness of lymphocytes and serum-inhibitory factors in patients with cancer. Cancer Res. 1973 Oct;33(10):2373–2377. [PubMed] [Google Scholar]
  15. Williams R. C., Jr, DeBoard J. R., Mellbye O. J., Messner R. P., Lindström F. D. Studies of T- and B-lymphocytes in patients with connective tissue diseases. J Clin Invest. 1973 Feb;52(2):283–295. doi: 10.1172/JCI107184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Williams R. C., Jr, Lies R. B., Messner R. P. Inhibition of mixed leukocyte culture responses by serum and gamma-globulin fractions from certain patients with connective tissue disorders. Arthritis Rheum. 1973 Sep-Oct;16(5):597–605. doi: 10.1002/art.1780160504. [DOI] [PubMed] [Google Scholar]

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