Articles |
Production in Lymphocytes From Healthy Individuals
From the Department of Medicine, Division of Rheumatology, Karolinska Hospital, Karolinska Institute, Stockholm, Sweden.
Correspondence to Johan Frostegård, Department of Medicine, Karolinska Hospital, Karolinska Institute, S-17176 Stockholm, Sweden.
Abstract The early stages of atherosclerosis
are characterized by penetration into the arterial intima
by both T lymphocytes and monocytes. Some of these T lymphocytes show
signs of activation, though the mechanisms by which they become
activated are not known. The monocytes develop into
macrophages and subsequently into foam cells filled with
oxidized LDL (oxLDL)-derived lipids. OxLDL has been found to exert
several proinflammatory effects, including enhanced adhesiveness of
endothelial cells and monocytes, chemotaxis of
monocytes and T cells, and T-cell activation. The enzyme-linked
immunospot (ELISPOT) assay has been shown to be a sensitive method for
detection of single cells secreting antibodies or cytokines.
Here we have used this method to characterize the T-cell
cytokine secretion pattern after exposure to oxLDL in vitro. In
peripheral blood mononuclear cells from healthy donors
(n=27), a significantly enhanced number of INF-
producing cells
was detected by ELISPOT (P<.001) after stimulation with 5
µg/mL oxLDL. In contrast, production of interleukin-4 was not
significantly enhanced after stimulation with oxLDL. OxLDL-induced
IFN-
secretion and T-cell proliferation were completely inhibited by
major histocompatibility complex (MHC) class II antibodies.
Furthermore, oxLDL was found to enhance the antibody secretion,
indicating B-cell activation. Our results indicate that oxLDL
activates T cells by an MHC class IIdependent mechanism. In
healthy individuals, oxLDL induces IFN-
, which is produced by T
helper type 1like cells. These findings demonstrate that oxLDL
induces a cell-dependent immune reaction, which may play an
important role in the development of atherosclerosis.
Key Words: T lymphocytes antibodies oxidized LDL atherosclerosis IFN-
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