Cytokine mRNA expression in B cells from bovine leukemia virus-infected cattle with persistent lymphocytosis

Cytokine ◽  
2004 ◽  
Vol 28 (1) ◽  
pp. 25-28 ◽  
Author(s):  
Marcel Amills ◽  
Junzo Norimine ◽  
Colleen A. Olmstead ◽  
Harris A. Lewin
2020 ◽  
Vol 64 (04) ◽  
pp. 451-456
Author(s):  
C. Úsuga-Monroy ◽  
L. G. González Herrera ◽  
J. J. Echeverri Zuluaga ◽  
F. J. Díaz ◽  
A. López-Herrera

2009 ◽  
Vol 71 (1) ◽  
pp. 49-54 ◽  
Author(s):  
Shinji YAMADA ◽  
Satoru KONNAI ◽  
Saiki IMAMURA ◽  
Martin SIMUUNZA ◽  
Mwelwa CHEMBENSOFU ◽  
...  

1998 ◽  
Vol 72 (8) ◽  
pp. 6917-6921 ◽  
Author(s):  
Dohun Pyeon ◽  
Gary A. Splitter

ABSTRACT Interleukin-12 (IL-12), a key cytokine in immune regulation, has an important role in activating the cell-mediated immune response in infectious diseases. Recently, a dichotomy between IL-12 and IL-10 regarding progression of a variety diseases has emerged. IL-12 activates type 1 cytokine production and has an antagonistic effect on type 2 cytokines. Here, by using quantitative competitive PCR, we show that peripheral blood mononuclear cells from bovine leukemia virus-infected animals in the alymphocytotic stage of disease express an increased amount of IL-12 p40 mRNA. In contrast, IL-12 p40 mRNA expression by cells from animals with late-stage disease, termed persistent lymphocytosis, was significantly decreased compared to that by normal and alymphocytotic animals. Interestingly, IL-12 p40 mRNA was also detected in tumor-bearing animals. IL-12 p40 expression occurred only in monocytes/macrophages, not B or T lymphocytes. The present study combined with previous findings suggest that IL-12 in bovine leukemia virus-infected animals may regulate production of other cytokines such as gamma interferon and IL-10 and the progression of bovine leukosis in animals that develop more advanced disease such as a persistent lymphocytosis of B cells or B-cell lymphosarcoma.


Author(s):  
Shiho TAKEZAWA ◽  
Masaki MAEZAWA ◽  
Satoko TSUZUKU ◽  
Junko KAWAKAMI ◽  
Yoshinao OOUCI ◽  
...  

2014 ◽  
Vol 95 (8) ◽  
pp. 1832-1842 ◽  
Author(s):  
Ryoyo Ikebuchi ◽  
Satoru Konnai ◽  
Tomohiro Okagawa ◽  
Asami Nishimori ◽  
Ayako Nakahara ◽  
...  

Bovine leukemia virus (BLV) induces abnormal B-cell proliferation and B-cell lymphoma in cattle, where the BLV provirus is integrated into the host genome. BLV-infected B-cells rarely express viral proteins in vivo, but short-term cultivation augments BLV expression in some, but not all, BLV-infected B-cells. This observation suggests that two subsets, i.e. BLV-silencing cells and BLV-expressing cells, are present among BLV-infected B-cells, although the mechanisms of viral expression have not been determined. In this study, we examined B-cell markers and viral antigen expression in B-cells from BLV-infected cattle to identify markers that may discriminate BLV-expressing cells from BLV-silencing cells. The proportions of IgMhigh B-cells were increased in blood lymphocytes from BLV-infected cattle. IgMhigh B-cells mainly expressed BLV antigens, whereas IgMlow B-cells did not, although the provirus load was equivalent in both subsets. Several parameters were investigated in these two subsets to characterize their cellular behaviour. Real-time PCR and microarray analyses detected higher expression levels of some proto-oncogenes (e.g. Maf, Jun and Fos) in IgMlow B-cells than those in IgMhigh B-cells. Moreover, lymphoma cells obtained from the lymph nodes of 14 BLV-infected cattle contained IgMlow or IgM− B-cells but no IgMhigh B-cells. To our knowledge, this is the first study to demonstrate that IgMhigh B-cells mainly comprise BLV-expressing cells, whereas IgMlow B-cells comprise a high proportion of BLV-silencing B-cells in BLV-infected cattle.


PLoS ONE ◽  
2021 ◽  
Vol 16 (9) ◽  
pp. e0256588
Author(s):  
Chihiro Ochiai ◽  
Sonoko Miyauchi ◽  
Yuta Kudo ◽  
Yuta Naruke ◽  
Syuji Yoneyama ◽  
...  

Bovine leukemia virus (BLV) is the causative agent of enzootic bovine leukosis (EBL), a malignant B cell lymphoma. However, the mechanisms of BLV-associated lymphomagenesis remain poorly understood. Here, after deep sequencing, we performed comparative analyses of B cell microRNAs (miRNAs) in cattle infected with BLV and those without BLV. In BLV-infected cattle, BLV-derived miRNAs (blv-miRNAs) accounted for 38% of all miRNAs in B cells. Four of these blv-miRNAs (blv-miR-B1-5p, blv-miR-B2-5p, blv-miR-B4-3p, and blv-miR-B5-5p) had highly significant positive correlations with BLV proviral load (PVL). The read counts of 90 host-derived miRNAs (bta-miRNAs) were significantly down-regulated in BLV-infected cattle compared to those in uninfected cattle. Only bta-miR-375 had a positive correlation with PVL in BLV-infected cattle and was highly expressed in the B cell lymphoma tissue of EBL cattle. There were a few bta-miRNAs that correlated with BLV tax/rex gene expression; however, BLV AS1 expression had a significant negative correlation with many of the down-regulated bta-miRNAs that are important for tumor development and/or tumor suppression. These results suggest that BLV promotes lymphomagenesis via AS1 and blv-miRNAs, rather than tax/rex, by down-regulating the expression of bta-miRNAs that have a tumor-suppressing function, and this downregulation is linked to increased PVL.


Virology ◽  
2002 ◽  
Vol 304 (1) ◽  
pp. 1-9 ◽  
Author(s):  
Marcel Amills ◽  
Vijayakumar Ramiya ◽  
Junzo Norimine ◽  
Colleen A. Olmstead ◽  
Harris A. Lewin

2001 ◽  
Vol 75 (4) ◽  
pp. 1689-1696 ◽  
Author(s):  
Glenn H. Cantor ◽  
Suzanne M. Pritchard ◽  
Franck Dequiedt ◽  
Luc Willems ◽  
Richard Kettmann ◽  
...  

ABSTRACT Bovine leukemia virus (BLV), a retrovirus related to human T-cell leukemia virus types 1 and 2, can induce persistent nonneoplastic expansion of the CD5+ B-cell population, termed persistent lymphocytosis (PL). As in human CD5+ B cells, we report here that CD5 was physically associated with the B-cell receptor (BCR) in normal bovine CD5+ B cells. In contrast, in CD5+ B cells from BLV-infected PL cattle, CD5 was dissociated from the BCR. In B cells from PL cattle, apoptosis decreased when cells were stimulated with antibody to surface immunoglobulin M (sIgM), while in B cells from uninfected cattle, apoptosis increased after sIgM stimulation. The functional significance of the CD5-BCR association was suggested by experimental dissociation of the CD5-BCR interaction by cross-linking of CD5. This caused CD5+ B cells from uninfected animals to decrease apoptosis when stimulated with anti-sIgM. In contrast, in CD5+ B cells from PL animals, in which CD5 was already dissociated from the BCR, there was no statistically significant change in apoptosis when CD5 was cross-linked and the cells were stimulated with anti-sIgM. Disruption of CD5-BCR interactions and subsequent decreased apoptosis and increased survival in antigenically stimulated B cells may be a mechanism of BLV-induced PL.


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