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Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1991 Sep;85(3):424–428. doi: 10.1111/j.1365-2249.1991.tb05743.x

Impaired T cell signal transduction through CD28 in a patient with idiopathic thrombocytopenia.

M Pérez-Blas 1, A Arnaiz-Villena 1, R Góngora 1, O G Segurado 1, J L Vivanco 1, J R Regueiro 1
PMCID: PMC1535620  PMID: 1654236

Abstract

We describe an infant whose peripheral blood mononuclear cells were unable to proliferate or synthesize IL-2 in response to a mitogenic combination of antibodies directed against CD2 and CD28. This peculiar defect, which has been stable to date, was attributed to an impairment in CD28-mediated T cell activation, because further comitogenic combinations containing anti-CD28 monoclonals also failed to induce normal proliferation of the patient's T cells. In contrast, proliferation after membrane stimulation (with anti-CD2, recombinant IL-2, or certain lectins) or transmembrane activation (with phorbol ester and calcium ionophore) was normal, suggesting that his lymphocytes did not have a general membrane or intracellular signalling impairment. A T cell line derived from the patient confirmed the existence of a severe defect in CD28-mediated T cell proliferation, but also showed a profound impairment in CD3-induced T cell proliferation. Other cell surface molecules like CD2 and CD25 were, in contrast, capable of transducing normal proliferation signals. As all relevant molecules were detectable by cytofluorography and immunoprecipitation, we conclude that the patient's lymphocytes had an intrinsic defect in the delivery of CD28-mediated signals which, in the absence of monocytes, also affected CD3-mediated proliferation. The study of this novel kind of immunodeficiency may help to unravel the complex interactions that take place among CD2, CD3 and CD28 during T cell activation. The presence of an idiopathic thrombocytopenia in the patient suggests the intriguing possibility of a role for CD28 in the maintenance of peripheral blood platelets levels, although alternative interpretations are not ruled out.

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Selected References

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  1. Alarcon B., Terhorst C., Arnaiz-Villena A., Perez-Aciego P., Regueiro J. R. Congenital T-cell receptor immunodeficiencies in man. Immunodefic Rev. 1990;2(1):1–16. [PubMed] [Google Scholar]
  2. Alcover A., Ramarli D., Richardson N. E., Chang H. C., Reinherz E. L. Functional and molecular aspects of human T lymphocyte activation via T3-Ti and T11 pathways. Immunol Rev. 1987 Feb;95:5–36. doi: 10.1111/j.1600-065x.1987.tb00498.x. [DOI] [PubMed] [Google Scholar]
  3. Briddell R. A., Hoffman R. Cytokine regulation of the human burst-forming unit-megakaryocyte. Blood. 1990 Aug 1;76(3):516–522. [PubMed] [Google Scholar]
  4. De Felice M., Giarrusso P. C., Lamberti A., Turco M. C., Valerio G., van Lier R. A., Yang S. Y., Ferrone S., Venuta S. Mitogenic activity of anti-CD28 MoAb CLB-CD28/1 on peripheral blood mononuclear cells and its cooperation with other anti-T cells MoAb in the activation of purified T lymphocytes. Tissue Antigens. 1990 Jul;36(1):12–18. doi: 10.1111/j.1399-0039.1990.tb01792.x. [DOI] [PubMed] [Google Scholar]
  5. Doita M., Maeda S., Kawai K., Hirohata K., Sugiyama T. Analysis of lymphocyte subsets of bone marrow in patients with rheumatoid arthritis by two colour immunofluorescence and flow cytometry. Ann Rheum Dis. 1990 Mar;49(3):168–171. doi: 10.1136/ard.49.3.168. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gillis S., Ferm M. M., Ou W., Smith K. A. T cell growth factor: parameters of production and a quantitative microassay for activity. J Immunol. 1978 Jun;120(6):2027–2032. [PubMed] [Google Scholar]
  7. Guba S. C., Stella G., Turka L. A., June C. H., Thompson C. B., Emerson S. G. Regulation of interleukin 3 gene induction in normal human T cells. J Clin Invest. 1989 Dec;84(6):1701–1706. doi: 10.1172/JCI114352. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hara T., Fu S. M., Hansen J. A. Human T cell activation. II. A new activation pathway used by a major T cell population via a disulfide-bonded dimer of a 44 kilodalton polypeptide (9.3 antigen). J Exp Med. 1985 Jun 1;161(6):1513–1524. doi: 10.1084/jem.161.6.1513. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. June C. H., Ledbetter J. A., Linsley P. S., Thompson C. B. Role of the CD28 receptor in T-cell activation. Immunol Today. 1990 Jun;11(6):211–216. doi: 10.1016/0167-5699(90)90085-n. [DOI] [PubMed] [Google Scholar]
  10. Kimura H., Ishibashi T., Uchida T., Maruyama Y., Friese P., Burstein S. A. Interleukin 6 is a differentiation factor for human megakaryocytes in vitro. Eur J Immunol. 1990 Sep;20(9):1927–1931. doi: 10.1002/eji.1830200909. [DOI] [PubMed] [Google Scholar]
  11. Meuer S. C., Hussey R. E., Fabbi M., Fox D., Acuto O., Fitzgerald K. A., Hodgdon J. C., Protentis J. P., Schlossman S. F., Reinherz E. L. An alternative pathway of T-cell activation: a functional role for the 50 kd T11 sheep erythrocyte receptor protein. Cell. 1984 Apr;36(4):897–906. doi: 10.1016/0092-8674(84)90039-4. [DOI] [PubMed] [Google Scholar]
  12. Mills G. B., Girard P., Grinstein S., Gelfand E. W. Interleukin-2 induces proliferation of T lymphocyte mutants lacking protein kinase C. Cell. 1988 Oct 7;55(1):91–100. doi: 10.1016/0092-8674(88)90012-8. [DOI] [PubMed] [Google Scholar]
  13. Moretta A., Pantaleo G., Lopez-Botet M., Moretta L. Involvement of T44 molecules in an antigen-independent pathway of T cell activation. Analysis of the correlations to the T cell antigen-receptor complex. J Exp Med. 1985 Sep 1;162(3):823–838. doi: 10.1084/jem.162.3.823. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Pierres A., Cerdan C., Lopez M., Mawas C., Olive D. "CD3low" human thymocyte populations can readily be triggered via the CD2 and/or CD28 activation pathways whereas the CD3 pathway remains nonfunctional. J Immunol. 1990 Feb 15;144(4):1202–1207. [PubMed] [Google Scholar]
  15. Regueiro J. R., López-Botet M., De Landazuri M. O., Alcami J., Corell A., Martín-Villa J. M., Vicario J. L., Arnaiz-Villena A. An in vivo functional immune system lacking polyclonal T-cell surface expression of the CD3/Ti(WT31) complex. Scand J Immunol. 1987 Dec;26(6):699–708. doi: 10.1111/j.1365-3083.1987.tb02306.x. [DOI] [PubMed] [Google Scholar]
  16. Weiss A., Imboden J., Hardy K., Manger B., Terhorst C., Stobo J. The role of the T3/antigen receptor complex in T-cell activation. Annu Rev Immunol. 1986;4:593–619. doi: 10.1146/annurev.iy.04.040186.003113. [DOI] [PubMed] [Google Scholar]

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