Literature DB >> 224787

Persistent lymphocytosis in cattle: its cause, nature and relation to lymphosarcoma.

J F Ferrer, R R Marshak, D A Abt, S J Kenyon.   

Abstract

Studies in well-characterized cattle populations strongly support the view that the bovine leukemia virus (BLV) is the causative agent of the adult (enzootic) form of bovine lymphosarcoma and persistent lymphocytosis (PL), and that host genetic factors play an important role in the development of these two conditions. On the other hand, the available information indicates that the genetic factors controlling the development of PL are frequently independent of those controlling the development of lymphosarcoma. There is no evidence that clinically normal cattle with PL harbor malignant cells or have any other clinical abnormality. In these animals lymphocytosis results from the expansion of two distinct subpopulations of non-neoplastic B lymphocytes, one of which is free of BLV. Long-term studies have shown that the large majority of cattle with PL do not develop lymphosarcoma even when kept to advanced age. These data indicate that PL is not a disease nor a preclinical stage of lymphosarcoma. Rather PL should be considered as a benign response to BLV infection which, although frequently associated with lymphosarcoma, is independant of it.

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Year:  1978        PMID: 224787

Source DB:  PubMed          Journal:  Ann Rech Vet        ISSN: 0003-4193


  18 in total

1.  Development of persistent lymphocytosis in cattle is closely associated with DRB2.

Authors:  M J van Eijk; J A Stewart-Haynes; J E Beever; R L Fernando; H A Lewin
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

2.  Progression to persistent lymphocytosis and tumor development in bovine leukemia virus (BLV)-infected cattle correlates with impaired proliferation of CD4+ T cells in response to gag- and env-encoded BLV proteins.

Authors:  O Orlik; G A Splitter
Journal:  J Virol       Date:  1996-11       Impact factor: 5.103

3.  Milk and fat production in dairy cattle influenced by advanced subclinical bovine leukemia virus infection.

Authors:  M C Wu; R D Shanks; H A Lewin
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

4.  Mutational analysis of bovine leukemia virus Rex: identification of a dominant-negative inhibitor.

Authors:  Eun-A Choi; Thomas J Hope
Journal:  J Virol       Date:  2005-06       Impact factor: 5.103

5.  The prevalence of proviral bovine leukemia virus in peripheral blood mononuclear cells at two subclinical stages of infection.

Authors:  M L Mirsky; C A Olmstead; Y Da; H A Lewin
Journal:  J Virol       Date:  1996-04       Impact factor: 5.103

6.  Integration of bovine leukaemia virus at all stages of enzootic bovine leukosis.

Authors:  J Coulston; R C Daniel; M F Lavin
Journal:  Arch Virol       Date:  1991       Impact factor: 2.574

7.  Milk and fat yields decline in bovine leukemia virus-infected Holstein cattle with persistent lymphocytosis.

Authors:  Y Da; R D Shanks; J A Stewart; H A Lewin
Journal:  Proc Natl Acad Sci U S A       Date:  1993-07-15       Impact factor: 11.205

8.  Increased cell proliferation, but not reduced cell death, induces lymphocytosis in bovine leukemia virus-infected sheep.

Authors:  Christophe Debacq; Becca Asquith; Pierre Kerkhofs; Daniel Portetelle; Arsène Burny; Richard Kettmann; Luc Willems
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-15       Impact factor: 11.205

9.  Association between BoLA and subclinical bovine leukemia virus infection in a herd of Holstein-Friesian cows.

Authors:  H A Lewin; M C Wu; J A Stewart; T J Nolan
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

10.  Overview of Mitigation Programs for Non-EU-Regulated Cattle Diseases in Austria.

Authors:  Franz-Ferdinand Roch; Beate Conrady
Journal:  Front Vet Sci       Date:  2021-06-15
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