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. 1984 Aug;52(4):611–620.

Altered lymphocyte recognition repertoire during ageing. III. Changes in MHC restriction patterns in parental T lymphocytes and diminution in T suppressor function.

R M Gorczynski, M Kennedy, S MacRae
PMCID: PMC1454669  PMID: 6235179

Abstract

Irradiated C57BL/6 and (C57BL/6 X C3H)F1 mice have been reconstituted with bone marrow prepared from young (2 month) or aged (24 month) C57BL/6 donors. Indirect examination of the T cell receptor for H-2d alloantigens on H-2b splenocytes of these reconstituted mice, using the suppression of the H-2b anti-H-2d response induced by (H-2b X H-2d)F1 anti-(H-2b anti-H-2d) suppressor cells, suggests that the allo-receptor repertoire derived from bone marrow of aged mice is different from that of T cells derived from young bone-marrow precursors. These observations were supported by direct evidence, from rosette formation with murine erythrocytes, for changes in the T cell receptor of these different (radiation-chimaera) sources of H-2b-T cells. Along with these subtle changes in the allo-receptor repertoire of T cells derived from bone marrow of aged mice grown in irradiated F1 hosts, there is a decrease (compared with mice reconstituted with bone marrow from young donors) in the apparent frequency of T cells recognizing antigen in association with the new MHC-restricting elements in these parent F1 chimaeras. Analysis of those cell subsets reported to be involved in the regulation of MLC responses suggests that some of the differences observed between T cell differentiation from bone-marrow stem cells of young or aged donors may in part be explained by a diminution in the production from bone marrow of aged mice of those cells important for homeostasis within the immune system.

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Selected References

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  1. Finberg R., Burakoff S. J., Cantor H., Benacerraf B. Biological significance of alloreactivity: T cells stimulated by Sendai virus-coated syngeneic cells specifically lyse allogeneic target cells. Proc Natl Acad Sci U S A. 1978 Oct;75(10):5145–5149. doi: 10.1073/pnas.75.10.5145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Gorczynski R. M., Benzing K., Krogsrud R., MacRae S., Price G. B. Alteration of allospecific t-cell receptors after differentiation from prethymic precursor cells in semiallogeneic environments. Cell Immunol. 1981 Aug;62(2):350–366. doi: 10.1016/0008-8749(81)90336-1. [DOI] [PubMed] [Google Scholar]
  3. Gorczynski R. M., Kennedy M., MacRae S. Alteration in lymphocyte recognition repertoire during aging. II. Changes in the expressed T-cell receptor repertoire in aged mice and the persistence of that change after transplantation to a new differentiative environment. Cell Immunol. 1983 Feb 1;75(2):226–241. doi: 10.1016/0008-8749(83)90322-2. [DOI] [PubMed] [Google Scholar]
  4. Gorczynski R. M., Kennedy M., MacRae S. Ontogeny of diversity in the receptor repertoire of murine cytotoxic lymphocytes. I. Comparison of recognition patterns of activated T cells of B10.D2 and B10.BR mice of different ages and analysis of changes in F1 hybrid and bone marrow radiation chimeras. Cell Immunol. 1982 Oct;73(1):44–58. doi: 10.1016/0008-8749(82)90434-8. [DOI] [PubMed] [Google Scholar]
  5. Gorczynski R. M., Kennedy M., MacRae S. Ontogeny of diversity in the receptor repertoire of murine cytotoxic lymphocytes. II. Fine specificity of negative regulation (suppression) of the allo-receptor repertoire in congenic B10.D2 mice. Cell Immunol. 1982 Oct;73(1):59–71. doi: 10.1016/0008-8749(82)90435-x. [DOI] [PubMed] [Google Scholar]
  6. Gorczynski R. M., MacRae S. Suppression of cytotoxic response to histoincompatible cells. II. Analysis of the role of two independent T suppressor pools in maintenance of neonatally induced allograft tolerance in mice. J Immunol. 1979 Mar;122(3):747–752. [PubMed] [Google Scholar]
  7. Gorczynski R. M., Macrae S. Microheterogeneity in regulatory circuits for T-cell alloresponsiveness. Immunology. 1981 Dec;44(4):827–846. [PMC free article] [PubMed] [Google Scholar]
  8. Krawinkel U., Cramer M., Melchers I., Imanishi-Kari T., Rajewsky K. Isolated hapten-binding receptors of sensitized lymphocytes. III. Evidence for idiotypic restriction of T-cell receptors. J Exp Med. 1978 May 1;147(5):1341–1347. doi: 10.1084/jem.147.5.1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Shearer G. M. Cell-mediated cytotoxicity to trinitrophenyl-modified syngeneic lymphocytes. Eur J Immunol. 1974 Aug;4(8):527–533. doi: 10.1002/eji.1830040802. [DOI] [PubMed] [Google Scholar]
  10. Sherman L. A. Influence of the major histocompatibility complex on the repertoire of allospecific cytolytic T lymphocytes. J Exp Med. 1982 Feb 1;155(2):380–389. doi: 10.1084/jem.155.2.380. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Sia D. Y., Parish C. R. Anti-self receptors. I. Direct detection of H-2L region-restricted receptors on murine thymocytes. J Exp Med. 1980 Mar 1;151(3):553–565. doi: 10.1084/jem.151.3.553. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Zinkernagel R. M., Althage A., Cooper S., Callahan G., Klein J. In irradiation chimeras, K or D regions of the chimeric host, not of the donor lymphocytes, determine immune responsiveness of antiviral cytotoxic T cells. J Exp Med. 1978 Sep 1;148(3):805–810. doi: 10.1084/jem.148.3.805. [DOI] [PMC free article] [PubMed] [Google Scholar]

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