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Published on: November 8, 2011
B-lymphocyte proliferation during bovine leukemia virus-induced persistent lymphocytosis is enhanced by
E S Trueblood1, W C Brown, G H Palmer
1Department of Veterinary Microbiology and Pathology, Washington State University, Pullman 99164, USA. est@vetmed.wsu.edu
Insights
Bovine leukemia virus (BLV) infection causes persistent lymphocytosis, a condition linked to increased Interleukin-2 (IL-2) production by T-lymphocytes. This IL-2 drives B-lymphocyte proliferation, suggesting a key role in the disease.
Area of Science:
- Immunology
- Veterinary Virology
- Cell Biology
Background:
- Bovine leukemia virus (BLV) causes persistent lymphocytosis, characterized by abnormal B-lymphocyte expansion.
- The role of cytokines in the microenvironment of BLV-induced lymphocytosis is not fully understood.
Purpose of the Study:
- To investigate the role of the cytokine microenvironment, specifically Interleukin-2 (IL-2), Interleukin-4 (IL-4), Interleukin-10 (IL-10), and Interferon-gamma (IFN-gamma) mRNA expression, in BLV-induced persistent lymphocytosis.
- To determine the impact of IL-2 on B-lymphocyte proliferation and viral protein expression in BLV-infected cattle.
Main Methods:
- Measured mRNA expression of IL-2, IL-4, IL-10, and IFN-gamma in stimulated peripheral blood mononuclear cells (PBMCs) from BLV-infected (lymphocytotic and non-lymphocytotic) and uninfected cows.
- Assessed IL-2 functional activity and the response of isolated B lymphocytes to recombinant cytokines and T-lymphocyte supernatants.
- Utilized polyclonal anti-IL-2 and anti-BLV antibodies to inhibit spontaneous proliferation of PBMCs.
Main Results:
- Significantly increased IL-2 and IL-10 mRNA expression and IL-2 functional activity were observed in PBMCs from persistently lymphocytotic cows upon stimulation.
- Recombinant IL-2 (rhIL-2) increased viral protein (p24) and IL-2 receptor expression in isolated B lymphocytes and enhanced B-lymphocyte proliferation.
- T-lymphocyte supernatant-induced B-lymphocyte proliferation was inhibited by anti-IL-2 antibody, and spontaneous lymphoproliferation was dependent on IL-2 and antigen.
Conclusions:
- Increased T-lymphocyte expression of IL-2 in BLV-infected cows is a critical factor contributing to the development and/or maintenance of persistent B lymphocytosis.
- The findings highlight IL-2-dependent and antigen-dependent mechanisms underlying BLV-induced lymphoproliferation.
Abstract:
Bovine leukemia virus (BLV)-induced persistent lymphocytosis is characterized by a polyclonal expansion of CD5+ B lymphocytes. To examine the role of the cytokine microenvironment in this virus-induced B-lymphocyte expansion, the expression of interleukin-2 (IL-2), IL-4, IL-10, and gamma interferon (IFN-gamma) mRNA, was measured in stimulated peripheral blood mononuclear cells from persistently lymphocytotic BLV-infected cows, nonlymphocytotic BLV-infected cows, and uninfected cows. IL-2 and IL-10 mRNA expression and IL-2 functional activity were significantly increased when peripheral blood mononuclear cells from persistently lymphocytotic cows were stimulated with concanavalin A (ConA). Additionally, during persistent lymphocytosis, peak IL-2 and IL-10 mRNA expression was delayed, and elevated expression was prolonged. To determine the potential biologic importance of increased IL-2 and IL-10 expression, the response of isolated B lymphocytes from persistently lymphocytotic cows to human recombinant cytokines and to cytokine-containing supernatants from isolated T lymphocytes was examined. While recombinant human IL-10 (rhIL-10) did not consistently induce detectable changes, rhIL-2 increased viral protein (p24) and IL-2 receptor expression in isolated B lymphocytes from persistently lymphocytotic cows. Additionally, rhIL-2 and supernatant from ConA-stimulated T lymphocytes enhanced B-lymphocyte proliferation. The stimulatory activity of the T-lymphocyte supernatant could be completely inhibited with a polyclonal anti-rhIL-2 antibody. Finally, polyclonal anti-rhIL-2 antibody, as well as anti-BLV antibody, inhibited spontaneous proliferation of peripheral blood mononuclear cells from persistently lymphocytotic cows, demonstrating that the spontaneous lymphoproliferation characteristic of BLV-induced persistent lymphocytosis is IL-2 dependent and antigen dependent. Collectively, these findings strongly suggest that increased T-lymphocyte expression of IL-2 in BLV-infected cows contributes to development and/or maintenance of persistent B lymphocytosis.
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