Skip to main content
Clinical and Experimental Immunology logoLink to Clinical and Experimental Immunology
. 1982 Dec;50(3):621–628.

Lymphocyte dysfunction in cartilage hair hypoplasia. II. Evidence for a cell cycle specific defect in T cell growth

G F Pierce, S H Polmar
PMCID: PMC1536810  PMID: 6984669

Abstract

Defects of in vitro B and T lymphocyte function and impaired delayed type hypersen-sitivity reactions, as well as an increased risk of lethal viral infections have been reported in cartilage hair hypoplasia (CHH), an autosomal recessive form of short limbed dwarfism. We have previously found an intrinsic proliferative defect that affected several cell types from CHH individuals. In order to further evaluate it we developed continuous T cell lines (CTCL) from CHH and normal individuals. The T cells from cultures of CHH and normal individuals were indistinguishable with respect to cell surface antigens characteristic of fully differentiated T cells, as defined by monoclonal antibody analysis. However, CHH T cells produced significantly less interleukin 2 (IL2) than normal T cells and the growth of CHH CTCL in response to exogenously supplied IL2 was markedly diminished (cell cycle 120-165 hr) compared to normal CTCL (cell cycle 48-60 hr). Furthermore, the exogenous IL2 was not absorbed from growth medium by CHH CTCL at the same rate as normal CTCL. Both production and utilization of IL2 are cell cycle specific events that occur during G1 phase before the onset of DNA synthesis (S phase). Thus, CHH T lymphocytes appear to have a defect related to G1 phase that results in a longer cell cycle for individual cells, and leads to decreased proliferation of the population. We postulate that this G1 phase defect is present in multiple cell types in CHH and that analysis of continuous T cell lines from CHH individuals may permit the identification of this defect.

Full text

PDF
621

Selected References

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

  1. Alvarez J. M., Silva A., de Landazuri M. O. Human T cell growth factor. I. Optimal conditions for its production. J Immunol. 1979 Sep;123(3):977–983. [PubMed] [Google Scholar]
  2. Birch R. E., Polmar S. H. Induction of Fc gamma receptors on a subpopulation of human T lymphocytes by adenosine and impromidine, an H2-histamine agonist. Cell Immunol. 1981 Jan 15;57(2):455–467. doi: 10.1016/0008-8749(81)90103-9. [DOI] [PubMed] [Google Scholar]
  3. Brooks R. F., Bennett D. C., Smith J. A. Mammalian cell cycles need two random transitions. Cell. 1980 Feb;19(2):493–504. doi: 10.1016/0092-8674(80)90524-3. [DOI] [PubMed] [Google Scholar]
  4. Castor L. N. A G1 rate model accounts for cell-cycle kinetics attributed to 'transition probability'. Nature. 1980 Oct 30;287(5785):857–859. doi: 10.1038/287857a0. [DOI] [PubMed] [Google Scholar]
  5. De Vries J. E., Vyth F. A., Mendelsohn J. T-cell growth factor-mediated proliferation of lymphocytes from a T-chronic lymphocytic leukaemia patient lacking mitogen and alloantigen responsiveness. Clin Exp Immunol. 1981 Feb;43(2):302–310. [PMC free article] [PubMed] [Google Scholar]
  6. Ferrarini M., Cadoni A., Franzi A. T., Ghigliotti C., Leprini A., Zicca A., Grossi C. E. Ultrastructure and cytochemistry of human peripheral blood lymphocytes. Similarities between the cells of the third population and TG lymphocytes. Eur J Immunol. 1980 Jul;10(7):562–570. doi: 10.1002/eji.1830100714. [DOI] [PubMed] [Google Scholar]
  7. Gelfand E. W., Lee J. J., Dosch H. M. Selective toxicity of purine deoxynucleosides for human lymphocyte growth and function. Proc Natl Acad Sci U S A. 1979 Apr;76(4):1998–2002. doi: 10.1073/pnas.76.4.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gillis S., Kozak R., Durante M., Weksler M. E. Immunological studies of aging. Decreased production of and response to T cell growth factor by lymphocytes from aged humans. J Clin Invest. 1981 Apr;67(4):937–942. doi: 10.1172/JCI110143. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Inouye H., Hank J. A., Alter B. J., Bach F. H. TCGF production for cloning and growth of functional human T lymphocytes. Scand J Immunol. 1980;12(2):149–154. doi: 10.1111/j.1365-3083.1980.tb00051.x. [DOI] [PubMed] [Google Scholar]
  10. Kurnick J. T., Hayward A. R., Altevogt P. Helper and suppressor-inducer activity of human T cells and their cloned progeny maintained in long-term culture. J Immunol. 1981 Apr;126(4):1307–1311. [PubMed] [Google Scholar]
  11. Larsson E. L. Mechanism of T cell activation. II. Antigen- and lectin-dependent acquisition of responsiveness to TCGF is a nonmitogenic, active response of resting T cells. J Immunol. 1981 Apr;126(4):1323–1326. [PubMed] [Google Scholar]
  12. Lux S. E., Johnston R. B., Jr, August C. S., Say B., Penchaszadeh V. B., Rosen F. S., McKusick V. A. Chronic neutropenia and abnormal cellular immunity in cartilage-hair hypoplasia. N Engl J Med. 1970 Jan 29;282(5):231–236. doi: 10.1056/NEJM197001292820501. [DOI] [PubMed] [Google Scholar]
  13. López-Botet M., Fontán G., Garcia Rodriguez M. C., de Landázuri M. O. Relationship between IL 2 synthesis and the proliferative response to PHA in different primary immunodeficiencies. J Immunol. 1982 Feb;128(2):679–683. [PubMed] [Google Scholar]
  14. MCKUSICK V. A., ELDRIDGE R., HOSTETLER J. A., RUANGWIT U., EGELAND J. A. DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA. Bull Johns Hopkins Hosp. 1965 May;116:285–326. [PubMed] [Google Scholar]
  15. Maizel A. L., Mehta S. R., Hauft S., Franzini D., Lachman L. B., Ford R. J. Human T lymphocyte/monocyte interaction in response to lectin: kinetics of entry into the S-phase. J Immunol. 1981 Sep;127(3):1058–1064. [PubMed] [Google Scholar]
  16. Pawelec G., Rehbein A., Müller C., Sonneborn H. H., Wernet P. Human T lymphocytes grown in T-cell growth factor: functional attributes in MLC, CML, PLT and allogeneic suppression. Immunology. 1981 Apr;42(4):529–540. [PMC free article] [PubMed] [Google Scholar]
  17. Pierce G. F., Polmar S. H. Lymphocyte dysfunction in cartilage-hair hypoplasia: evidence for an intrinsic defect in cellular proliferation. J Immunol. 1982 Aug;129(2):570–575. [PubMed] [Google Scholar]
  18. Polmar S. H. Metabolic aspects of immunodeficiency disease. Semin Hematol. 1980 Jan;17(1):30–43. [PubMed] [Google Scholar]
  19. Raivio K. O. The biochemical basis of immunodeficiency disease. Eur J Pediatr. 1980 Oct;135(1):13–20. doi: 10.1007/BF00445887. [DOI] [PubMed] [Google Scholar]
  20. Ranki A., Perheentupa J., Andersson L. C., Häyry P. In vitro T- and B-cell reactivity in cartilage hair hypoplasia. Clin Exp Immunol. 1978 May;32(2):352–360. [PMC free article] [PubMed] [Google Scholar]
  21. Robb R. J., Munck A., Smith K. A. T cell growth factor receptors. Quantitation, specificity, and biological relevance. J Exp Med. 1981 Nov 1;154(5):1455–1474. doi: 10.1084/jem.154.5.1455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Ruscetti F. W., Gallo R. C. Human T-lymphocyte growth factor: regulation of growth and function of T lymphocytes. Blood. 1981 Mar;57(3):379–394. [PubMed] [Google Scholar]
  23. Smith K. A., Lachman L. B., Oppenheim J. J., Favata M. F. The functional relationship of the interleukins. J Exp Med. 1980 Jun 1;151(6):1551–1556. doi: 10.1084/jem.151.6.1551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Stadler B. M., Dougherty S. F., Farrar J. J., Oppenheim J. J. Relationship of cell cycle to recovery of IL 2 activity from human mononuclear cells, human and mouse T cell lines. J Immunol. 1981 Nov;127(5):1936–1940. [PubMed] [Google Scholar]
  25. Strausser J. L., Rosenberg S. A. In vitro growth of cytotoxic human lymphocytes. I. Growth of cells sensitized in vitro to alloantigens. J Immunol. 1978 Oct;121(4):1491–1495. [PubMed] [Google Scholar]
  26. Trojak J. E., Polmar S. H., Winkelstein J. A., Hsu S., Francomano C., Pierce G. F., Scillian J. J., Gale A. N., McKusick V. A. Immunologic studies of cartilage-hair hypoplasia in the Amish. Johns Hopkins Med J. 1981 Apr;148(4):157–164. [PubMed] [Google Scholar]
  27. Virolainen M., Savilahti E., Kaitila I., Perheentupa J. Cellular and humoral immmunity in cartilage-hair hypoplasia. Pediatr Res. 1978 Oct;12(10):961–966. doi: 10.1203/00006450-197810000-00002. [DOI] [PubMed] [Google Scholar]

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

RESOURCES