Literature DB >> 15033

Cell lines from old immunodeficient donors give normal responses in young recipients.

D E Harrison, C M Astle, J W Doubleday.   

Abstract

Two different immune responses were compared in spleen cells obtained from old and young CBA/HT6J mice. Spleen cells from old mice (23 to 33 months) responded about half as well as did spleen cells from young mice (4 to 10 months) in the adoptive transfer anti-sheep red blood cell (SRBC) plague-forming assay, and caused slightly less than half the uptake of tritiated thymidine in response to phytohemagglutinin (PHA) in vitro. Marrow stem cell from some of the old and young mice whose splenic immune responses were tested were transplanted into irradiated young CBA/CaJ recipients. Seven to 17 weeks later these same immune responses were tested in the spleen cells of these young recipients, and the T6 chromosome marker was used to identify donor cells. Old animals' responses varied greatly, perhaps due to suppressing cells or factors in some individuals. Therefore, cells were never pooled and the responses of receipients were compared to the responses of the donor whose marrow had populated them. The response for a particular old donor, or for the recipients of its stem cells, was divided by the response for the young control used with that donor, or for its stem cell recipients. This was called the old/young ratio. With original donors with an old/young ratio for the SRBC response of (mean +/- S.D.) 0.35 +/- 0.14, The old/young ratio for that same response in the recipients was significantly improved to 1.26 +/- 0.71. In original donors with an old/young ratio for the PHA response of 0.44 +/- 0.17, the old/young ratio in the recipients improved significantly to 0.86 +/- 0.27. Thus, little or none of the decline with age in these immune responses was intrinsic to the old lymphoid stem cells.

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Year:  1977        PMID: 15033

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  9 in total

Review 1.  Senescence of hematopoietic stem cells and bone marrow failure.

Authors:  Jichun Chen
Journal:  Int J Hematol       Date:  2005-10       Impact factor: 2.490

2.  Loss of proliferative capacity in immunohemopoietic stem cells caused by serial transplantation rather than aging.

Authors:  D E Harrison; C M Astle; J A Delaittre
Journal:  J Exp Med       Date:  1978-05-01       Impact factor: 14.307

3.  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

4.  Loss of stem cell repopulating ability upon transplantation. Effects of donor age, cell number, and transplantation procedure.

Authors:  D E Harrison; C M Astle
Journal:  J Exp Med       Date:  1982-12-01       Impact factor: 14.307

5.  Ultimate erythropoietic repopulating abilities of fetal, young adult, and old adult cells compared using repeated irradiation.

Authors:  D E Harrison; C M Astle; C Lerner
Journal:  J Exp Med       Date:  1984-09-01       Impact factor: 14.307

6.  Long-term erythropoietic repopulating ability of old, young, and fetal stem cells.

Authors:  D E Harrison
Journal:  J Exp Med       Date:  1983-05-01       Impact factor: 14.307

7.  Bone marrow function. I. Peripheral T cells are responsible for the increased auto-antiidiotype response of older mice.

Authors:  Y T Kim; E A Goidl; C Samarut; M E Weksler; G J Thorbecke; G W Siskind
Journal:  J Exp Med       Date:  1985-05-01       Impact factor: 14.307

8.  Production of auto-antiidiotypic antibody during the normal immune response. VII. Analysis of the cellular basis for the increased auto-antiidiotype antibody production by aged mice.

Authors:  E A Goidl; J W Choy; J J Gibbons; M E Weksler; G J Thorbecke; G W Siskind
Journal:  J Exp Med       Date:  1983-05-01       Impact factor: 14.307

9.  Hematotoxicity and carcinogenicity of inhaled benzene.

Authors:  E P Cronkite; R T Drew; T Inoue; Y Hirabayashi; J E Bullis
Journal:  Environ Health Perspect       Date:  1989-07       Impact factor: 9.031

  9 in total

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