Literature DB >> 376720

Defective tumoricidal capacity of macrophages from A/J mice. I. Characterization of the macrophage cytotoxic defect after in vivo and in vitro activation stimuli.

D Boraschi, M S Meltzer.   

Abstract

Macrophages from A/J mice fail to develop tumoricidal activity after any of several in vivo or in vitro treatments that activate cells from C3H/HeN mice. Peritoneal macrophages from A/J mice treated i.p. with viable Mycobacterium bovis, strain BCG, killed Corynebacterium parvum, or pyran copolymer fail to develop in vitro tumoricidal activity; varying the numbers of macrophages from treated mice added to target cells, or the dose and time of treatment, or the treatment schedule of these in vivo activation stimuli did not evoke cytotoxic activity. Moreover, cytotoxic activity by macrophages from A/J mice was not observed with any of four target cell lines derived from three different mouse strains. In vitro treatment of peritoneal exudate macrophages from A/J mice with lymphokine-rich supernatants, bacterial endotoxins, or T cell mitogens was also ineffective; varying the numbers of treated macrophages added to target cells, the dose of in vitro activation stimuli, or the time of treatment did not evoke cytotoxic activity. Thus, A/J mice exhibit a profound defect in macrophage tumoricidal capacity to both in vivo and in vitro activation stimuli over a wide range of experimental conditions.

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Year:  1979        PMID: 376720

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


  10 in total

1.  A novel rat monoclonal antibody reactive with murine tumoricidal Kupffer cells and activated peritoneal macrophages from BCG-infected mice.

Authors:  A Someya
Journal:  Immunology       Date:  1986-04       Impact factor: 7.397

2.  Tumor progression stage and anatomical site regulate tumor-associated macrophage and bone marrow-derived monocyte polarization.

Authors:  Elizabeth F Redente; Lori D Dwyer-Nield; Daniel T Merrick; Komal Raina; Rajesh Agarwal; William Pao; Pamela L Rice; Kenneth R Shroyer; Alvin M Malkinson
Journal:  Am J Pathol       Date:  2010-04-29       Impact factor: 4.307

3.  II. Tumor growth at sites of inflammation induced by mitogens in mice.

Authors:  M Nelson; D S Nelson
Journal:  Am J Pathol       Date:  1981-08       Impact factor: 4.307

4.  Natural resistance to infection with Legionella pneumophila: chromosomal localization of the Lgn1 susceptibility gene.

Authors:  M C Beckers; S Yoshida; K Morgan; E Skamene; P Gros
Journal:  Mamm Genome       Date:  1995-08       Impact factor: 2.957

5.  Rapid killing of actinomycin D-treated tumour cells by mononuclear phagocytes: reactivity in mouse strains with defective classical tumour cytotoxicity.

Authors:  F Collota; L Bersani; N Polentarutti; A Mantovani
Journal:  Immunology       Date:  1986-02       Impact factor: 7.397

6.  IFN-beta-induced reduction of superoxide anion generation by macrophages.

Authors:  D Boraschi; P Ghezzi; M Salmona; A Tagliabue
Journal:  Immunology       Date:  1982-04       Impact factor: 7.397

7.  Genetic control of natural resistance in mouse macrophages regulating intracellular Legionella pneumophila multiplication in vitro.

Authors:  S Yoshida; Y Goto; Y Mizuguchi; K Nomoto; E Skamene
Journal:  Infect Immun       Date:  1991-01       Impact factor: 3.441

8.  Effect of acute nutritional deprivation on immune function in mice. I. Macrophages.

Authors:  E J Wing; L K Barczynski; S M Boehmer
Journal:  Immunology       Date:  1983-03       Impact factor: 7.397

9.  Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4).

Authors:  I Smirnova; A Poltorak; E K Chan; C McBride; B Beutler
Journal:  Genome Biol       Date:  2000-04-27       Impact factor: 13.583

10.  Differences in tumour necrosis factor productive ability among rodents.

Authors:  K Haranaka; N Satomi; A Sakurai
Journal:  Br J Cancer       Date:  1984-10       Impact factor: 7.640

  10 in total

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