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

Journal of Virology
|April 3, 1998
PubMed

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.

Related Concept Videos

Cells of the Adaptive Immune Response01:23

Cells of the Adaptive Immune Response

The T and B lymphocytes of the adaptive immune system develop from common lymphoid progenitor cells in the bone marrow. These progenitors give rise to precursors that eventually develop into both T and B lymphocytes. As these precursors mature, they gain the ability to detect and respond to foreign antigens in the body, a process known as immunocompetence. Additionally, these precursors acquire self-tolerance, a process that ensures they do not react to self-antigens. This intricate system...
T Cell Activation and Clonal Selection01:22

T Cell Activation and Clonal Selection

T cells are integral to our adaptive immune system, recognizing and effectively responding to foreign antigens. T cell activation and clonal selection are pivotal in orchestrating this immune response. This article elucidates these mechanisms, detailing the roles of cluster of differentiation (CD) markers, major histocompatibility complex (MHC) molecules, costimulatory signals, and the process of clonal selection.
Naive T cells that have not yet encountered an antigen express two primary CD...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...