Literature DB >> 6213555

Studies on the syngeneic mixed lymphocyte reaction. II. Decline in he syngeneic mixed lymphocyte reaction with age.

J K Gutowski, M E Weksler.   

Abstract

The syngeneic mixed lymphocyte reaction (SMLR) is the proliferative response of T lymphocytes cultured with syngeneic non-T lymphocytes. In previous studies, we found that the SMLR reaches adult level of activity at 4 weeks of age in BALB/c mice. We now report that the SMLR declines with age in this strain. The decline was first documented at 12 months of age, when non-T spleen cells were less able to stimulate young adult T cells than were non-T cells from 2 to 3 month-old mice. Splenic T cells from 12 month old mice were as responsive as splenic T cells from 2 to 3 months old mice. By 24 months of age, mice had no significant SMLR activity. Splenic T cells from 24 month old mice did not respond and splenic non-T cells did not stimulate SMLR when cultured with cells from young adult mice. Finally, suppressor cells were demonstrated in spleen cells preparations from 24 month old mice and may explain or contribute to the impaired SMLR in these animals.

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Mesh:

Year:  1982        PMID: 6213555      PMCID: PMC1555476     

Source DB:  PubMed          Journal:  Immunology        ISSN: 0019-2805            Impact factor:   7.397


  35 in total

1.  The cellular basis of the impaired autologous mixed lymphocyte reaction in patients with systemic lupus erythematosus.

Authors:  M M Kuntz; J B Innes; M E Weksler
Journal:  J Clin Invest       Date:  1979-01       Impact factor: 14.808

2.  Specificity and suppressor function of human T cells responsive to autologous non-T cells.

Authors:  T Sakane; I Green
Journal:  J Immunol       Date:  1979-08       Impact factor: 5.422

3.  Induction of suppressor activity in the autologous mixed lymphocyte reaction and in cultures with concanavalin A.

Authors:  J B Innes; M M Kuntz; Y T Kim; M E Weksler
Journal:  J Clin Invest       Date:  1979-12       Impact factor: 14.808

4.  Age related changes in the in vitro immune response: increased suppressor activity in immature and aged mice.

Authors:  R H DeKruyff; Y T Kim; G W Siskind; M E Weksler
Journal:  J Immunol       Date:  1980-07       Impact factor: 5.422

5.  T cells and macrophages involved in the autologous mixed lymphocyte reaction are required for the response to conventional antigen.

Authors:  P B Hausman; H V Raff; R C Gilbert; L J Picker; J D Stobo
Journal:  J Immunol       Date:  1980-09       Impact factor: 5.422

6.  Activation of suppressor T cells in human autologous mixed lymphocyte culture.

Authors:  J B Smith; R P Knowlton
Journal:  J Immunol       Date:  1979-07       Impact factor: 5.422

7.  Syngeneic mixed lymphocyte reaction in mice: strain distribution, kinetics, participating cells, and absence in NZB mice.

Authors:  J B Smith; R D Pasternak
Journal:  J Immunol       Date:  1978-11       Impact factor: 5.422

8.  Immunological senescence. I. The role of suppressor cells.

Authors:  J C Roder; A K Duwe; D A Bell; S K Singhal
Journal:  Immunology       Date:  1978-11       Impact factor: 7.397

9.  Immunologic studies of aging. V. Impaired proliferation of PHA responsive human lymphocytes in culture.

Authors:  J M Hefton; G J Darlington; B A Casazza; M E Weksler
Journal:  J Immunol       Date:  1980-09       Impact factor: 5.422

10.  Immunological studies of aging. IV. The contribution of thymic involution to the immune deficiencies of aging mice and reversal with thymopoietin32-36.

Authors:  M C Weksler; J D Innes; G Goldstein
Journal:  J Exp Med       Date:  1978-10-01       Impact factor: 14.307

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  1 in total

1.  T cell proliferation induced by anti-self-I-A-specific T cell hybridomas. Evidence of a T cell network.

Authors:  D W Kennedy; C Russo; Y T Kim; M E Weksler
Journal:  J Exp Med       Date:  1986-08-01       Impact factor: 14.307

  1 in total

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