Literature DB >> 2787777

Production of auto-anti-idiotype antibody during the normal immune response. XIV. Evidence for the antigen-independent operation of the idiotype network.

Y T Kim1, T Deblasio, G J Thorbecke, M E Weksler, G W Siskind.   

Abstract

We have previously shown that that idiotype (Id) repertoire expressed by old mice is different from that of young mice after immunization with trinitrophenylated Ficoll. Older mice also produce more auto-anti-Id antibodies than do young mice. Mice surviving a normally lethal dose of radiation (800 rads) as result of partial shielding of their bone marrow slowly recover immune function, after the repopulation of their peripheral lymphoid system by bone marrow precursor cells. Aged mice subjected to such a procedure produce low auto-anti-Id responses, like those of young mice. However, transfer of splenic T cells from old donors into such mice increases the magnitude of the auto-anti-Id response. In the present studies, we show that the age-related shift in Id expression is also determined by the age of the donor T cells. Furthermore, we show in serial cell transfer studies that the peripheral T-cell population of old mice modifies the level of the auto-anti-Id response in the absence of antigen. The results thus provide evidence for the normal, in vivo, operation of an Id-anti-Id network between B and T lymphocytes.

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Year:  1989        PMID: 2787777      PMCID: PMC1385256     

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


  25 in total

1.  Impaired delayed hypersensitivity in an aging population. Association with antinuclear reactivity and rheumatoid factor.

Authors:  D S Waldorf; R F Willkens; J L Decker
Journal:  JAMA       Date:  1968-03-04       Impact factor: 56.272

Review 2.  Immunologicc activity of the aged.

Authors:  T Makinodan; E H Perkins; M G Chen
Journal:  Adv Gerontol Res       Date:  1971

3.  Antitrinitrophenyl (TNP) plaque assay. Primary response of Balb/c mice to soluble and particulate immunogen.

Authors:  M B Rittenberg; K L Pratt
Journal:  Proc Soc Exp Biol Med       Date:  1969-11

4.  Production of auto-anti-idiotypic antibody during the normal immune response. XII. An enzyme-linked immunosorbent assay for auto-anti-idiotype antibody.

Authors:  J J Gibbons; E A Goidl; G M Shepherd; G J Thorbecke; G W Siskind
Journal:  J Immunol Methods       Date:  1985-05-23       Impact factor: 2.303

5.  Ontogeny of B lymphocyte function. VIII. Failure of thymus cells from aged donors to induce the functional maturation of B lymphocytes from immature donors.

Authors:  M R Szewczuk; R H DeKruyff; E A Goidl; M E Weksler; G W Siskind
Journal:  Eur J Immunol       Date:  1980-12       Impact factor: 5.532

6.  Production of auto-anti-idiotypic antibody during the normal immune response. VI. Hapten augmentation of plaque formation and hapten-reversible inhibition of plaque formation as assays for anti-idiotype antibody.

Authors:  E A Goidl; T Hayama; G M Shepherd; G W Siskind; G J Thorbecke
Journal:  J Immunol Methods       Date:  1983-03-11       Impact factor: 2.303

7.  Production of auto-anti-idiotypic antibody during the normal immune response: changes in the auto-anti-idiotypic antibody response and the idiotype repertoire associated with aging.

Authors:  E A Goidl; G J Thorbecke; M E Weksler; G W Siskind
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

8.  Loss of immune competence with age may be due to auto-anti-idiotypic antibody regulation.

Authors:  M R Szewczuk; R J Campbell
Journal:  Nature       Date:  1980-07-10       Impact factor: 49.962

9.  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

10.  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

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