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. 1983 Dec;50(4):519–528.

The human thymus in ageing: histologic involution paralleled by increased mitogen response and by enrichment of OKT3+ lymphocytes.

C D Baroni, M Valtieri, A Stoppacciaro, L P Ruco, S Uccini, C Ricci
PMCID: PMC1454384  PMID: 6606611

Abstract

In the present study, based on 24 individuals aged 5-61 years, the histological pattern of the thymus has been determined and correlated to the thymus lymphocyte in-vitro responses to phytohaemagglutinin (PHA) and concanavalin A (Con A). It has been found that lymphocytes from histologically involuted thymus were significantly more responsive to PHA and Con A stimulation than lymphocytes from histologically normal thymus. These data indicate that thymus age-dependent involution is associated with increased lymphocyte in-vitro reactivity. In addition, in 10 cases the relative proportions of the thymus lymphocyte subpopulations have been determined by the use of monoclonal antibodies OKT3, OKT4, OKT6 and OKT8. These results have been correlated to the histology of the organ and to the mitogen responsiveness of thymus lymphocytes. In normal thymus the majority of the cells were OKT6+, while there were lower numbers were OKT3+. However, in involuted thymus, OKT3+ lymphocytes prevailed over OKT6+ cells. Furthermore, a direct relationship between the proportion of OKT3+ lymphocytes and the response to mitogens has been observed. These findings indicate that the increased mitogen response noticed in histologically involuted thymus is accompanied by an OKT3+-cell enrichment which is paralleled by a depletion of OKT6+ cells.

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Selected References

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  1. Baroni C. D., Fabris N., Bertoli G. Effects of hormones on development and function of lymphoid tissues. Synergistic action of thyroxin and somatotropic hormone in pituitary dwarf mice. Immunology. 1969 Aug;17(2):303–314. [PMC free article] [PubMed] [Google Scholar]
  2. Baroni C. D., Rigato P., Ruco L., Uccini S., Mineo T., Ricci C. PHA and ConA lymphocyte response in normal, hyperplastic and neoplastic human thymus: morphologic and functional correlations. Cancer. 1980 Nov 1;46(9):2055–2061. doi: 10.1002/1097-0142(19801101)46:9<2055::aid-cncr2820460925>3.0.co;2-s. [DOI] [PubMed] [Google Scholar]
  3. Baroni C. D., Ruco L., Uccini S., Foschi A., Occhionero M., Marcorelli E. Tissue T-lymphocytes in untreated Hodgkin's disease: morphologic and functional correlations in spleens and lymph nodes. Cancer. 1982 Jul 15;50(2):259–268. doi: 10.1002/1097-0142(19820715)50:2<259::aid-cncr2820500216>3.0.co;2-b. [DOI] [PubMed] [Google Scholar]
  4. Baroni C., Fabris N., Bertoli G. Age dependency of the primary immune response in the hereditary pituitary dwarf and normal Snell-Bagg mouse. Experientia. 1967 Dec 15;23(12):1059–1060. doi: 10.1007/BF02136450. [DOI] [PubMed] [Google Scholar]
  5. Bellamy D., Mohamed K. A comparative study of age involution of the bursa of Fabricius an thymus in birds. Thymus. 1982 Feb;4(2):107–114. [PubMed] [Google Scholar]
  6. Bentwich Z., Douglas S. D., Siegal F. P., Kunkel H. G. Human lymphocyte-sheep erythrocyte rosette formation: some characteristics of the interaction. Clin Immunol Immunopathol. 1973 Jul;1(4):511–522. doi: 10.1016/0090-1229(73)90007-x. [DOI] [PubMed] [Google Scholar]
  7. Chan C., Sainte-Marie G. Distribution and morphology of the subcapsular and reticular cells of the ten-week-old rat thymus. J Anat. 1968 Mar;102(Pt 3):477–491. [PMC free article] [PubMed] [Google Scholar]
  8. Gery I., Gershon R. K., Waksman B. H. Potentiation of cultured mouse thymocyte responses by factors released by peripheral leucocytes. J Immunol. 1971 Dec;107(6):1778–1780. [PubMed] [Google Scholar]
  9. Hayward A. R., Kurnick J. T., Clarke D. R. T cell growth factor-enhanced PHA response of human thymus cells: requirement for T3+ cells. J Immunol. 1981 Nov;127(5):2079–2082. [PubMed] [Google Scholar]
  10. Janossy G., Tidman N., Papageorgiou E. S., Kung P. C., Goldstein G. Distribution of t lymphocyte subsets in the human bone marrow and thymus: an analysis with monoclonal antibodies. J Immunol. 1981 Apr;126(4):1608–1613. [PubMed] [Google Scholar]
  11. MILLER J. F. Immunological function of the thymus. Lancet. 1961 Sep 30;2(7205):748–749. doi: 10.1016/s0140-6736(61)90693-6. [DOI] [PubMed] [Google Scholar]
  12. MILLER J. F. THE THYMUS AND THE DEVELOPMENT OF IMMUNOLOGIC RESPONSIVENESS. Science. 1964 Jun 26;144(3626):1544–1551. doi: 10.1126/science.144.3626.1544. [DOI] [PubMed] [Google Scholar]
  13. Miller J. F. Effect of thymectomy in adult mice on immunological responsiveness. Nature. 1965 Dec 25;208(5017):1337–1338. doi: 10.1038/2081337a0. [DOI] [PubMed] [Google Scholar]
  14. Naparstek Y., Holoshitz J., Eisenstein S., Reshef T., Rappaport S., Chemke J., Ben-Nun A., Cohen I. R. Effector T lymphocyte line cells migrate to the thymus and persist there. Nature. 1982 Nov 18;300(5889):262–264. doi: 10.1038/300262a0. [DOI] [PubMed] [Google Scholar]
  15. Oosterom R., Kater L., Oosterom J. Effects of human thymic epithelial-conditioned medium on mitogen responsiveness of human and mouse lymphocytes. Clin Immunol Immunopathol. 1979 Apr;12(4):460–470. doi: 10.1016/0090-1229(79)90051-5. [DOI] [PubMed] [Google Scholar]
  16. Oosterom R., Kater L. The thymus in the aging individual. I. Mitogen responsiveness of human thymocytes. Clin Immunol Immunopathol. 1981 Feb;18(2):187–194. doi: 10.1016/0090-1229(81)90024-6. [DOI] [PubMed] [Google Scholar]
  17. Oosterom R., Kater L. The thymus in the aging individual. II. Thymic epithelial function in vitro in aging and in thymus pathology. Clin Immunol Immunopathol. 1981 Feb;18(2):195–202. doi: 10.1016/0090-1229(81)90025-8. [DOI] [PubMed] [Google Scholar]
  18. Piantelli M., Lauriola L., Maggiano N., Ranelletti F. O., Musiani P. Role of interleukins 1 and 2 on human thymocyte mitogen activation. Cell Immunol. 1981 Nov 1;64(2):337–349. doi: 10.1016/0008-8749(81)90485-8. [DOI] [PubMed] [Google Scholar]
  19. Simpson J. G., Gray E. S., Beck J. S. Age involution in the normal human adult thymus. Clin Exp Immunol. 1975 Feb;19(2):261–265. [PMC free article] [PubMed] [Google Scholar]
  20. Singh J., Singh A. K. Age-related changes in human thymus. Clin Exp Immunol. 1979 Sep;37(3):507–511. [PMC free article] [PubMed] [Google Scholar]
  21. Weissman I. L. Thymus cell maturation. Studies on the origin of cortisone-resistant thymic lymphocytes. J Exp Med. 1973 Feb 1;137(2):504–510. doi: 10.1084/jem.137.2.504. [DOI] [PMC free article] [PubMed] [Google Scholar]

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