Literature DB >> 1093967

Age-related decline in the antibody response to E. coli lipopolysaccharide in New Zealand Black mice.

M J Blankwater, L A Levert, W Hijmans.   

Abstract

A thymus-independent immune function in ageing NZB and BALB/c mice was compared by measuring the antibody response to E. coli lipopolysaccharide (LPS). Since it was found that 10-13 month-old NZB mice was particularly sensitive to LPS, this antigen had to be detoxified by alkali treatment. The anti-LPS splenic plaque-forming cell (PFC) response of NZB mice decreases with age and was lower than that of BALB/c mice in all age groups studied. The response of 4- and 10-month-old NZB mice showed an irregular time course and a number of mice showed no response. The present results indicate that, besides an impairment of T-cell functions, an impairment on the B-cell level must also be considered in ageing NZB mice.

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Year:  1975        PMID: 1093967      PMCID: PMC1445920     

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


  37 in total

Review 1.  The immunology and pathology of NZB mice.

Authors:  J B Howie; B J Helyer
Journal:  Adv Immunol       Date:  1968       Impact factor: 3.543

2.  Regulation of antibody synthesis against Escherichia coli endotoxin. II. Specificity, dose requirements and duration of paralysis induced in adult mice.

Authors:  S Britton
Journal:  Immunology       Date:  1969-04       Impact factor: 7.397

3.  Deficient immunologic functions of NZB mice.

Authors:  O Stutman; E J Yunis; R A Good
Journal:  Proc Soc Exp Biol Med       Date:  1968-04

4.  Further improvements in the plaque technique for detecting single antibody-forming cells.

Authors:  A J Cunningham; A Szenberg
Journal:  Immunology       Date:  1968-04       Impact factor: 7.397

5.  Immune response to a soluble protein antigen in NZB mice.

Authors:  D M Weir; W McBride; J D Naysmith
Journal:  Nature       Date:  1968-09-21       Impact factor: 49.962

6.  Response of NZB and NZB-NZW spleen cells to mitogenic agents.

Authors:  B G Leventhal; N Talal
Journal:  J Immunol       Date:  1970-04       Impact factor: 5.422

7.  Absorption of guinea pig serum with agar. A method for elimination of itscytotoxicity for murine thymus cells.

Authors:  A Cohen; M Schlesinger
Journal:  Transplantation       Date:  1970-07       Impact factor: 4.939

8.  Response of NZB mice to foreign antigen and development of autoimmune disease.

Authors:  J I Morton; B V Siegel
Journal:  J Reticuloendothel Soc       Date:  1969-02

9.  Increased 7S antibody response to sheep erythrocytes in the 2-month-old NZB mouse.

Authors:  J Baum
Journal:  Clin Exp Immunol       Date:  1969-09       Impact factor: 4.330

10.  Progressive loss in vitro of cellular immunity with ageing in strains of mice susceptible to autoimmune disease.

Authors:  G E Rodey; R A Good; E J Yunis
Journal:  Clin Exp Immunol       Date:  1971-09       Impact factor: 4.330

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  3 in total

1.  Age-related humoral antibody responses of AKR/J mice to T-cell dependent and independent antigens.

Authors:  B A Hatten; H Dunton
Journal:  Immunology       Date:  1978-11       Impact factor: 7.397

2.  The immune response in NZB mice of different ages to thymus-dependent and thymus-independent phosphorylcholine antigens.

Authors:  J P McKearn; G W Miller; J Quintáns
Journal:  Immunology       Date:  1978-06       Impact factor: 7.397

3.  Lymphocyte nucleoli activation as a marker of autoimmune disorder development. I. Observation in NZB mice.

Authors:  L Korcáková; J Rovenský; J Pekárek; V Haskova
Journal:  Immunology       Date:  1976-04       Impact factor: 7.397

  3 in total

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