Aberrant expression of Fas ligand on anti-DNA autoantibody secreting B lymphocytes in patients with systemic lupus erythematosus: "Immune privilege"-like state of the autoreactive B cells
H. Nagafuchi, S. Wakisaka, Y. Takeba, M. Takeno, T. Sakane, N. Suzuki
Departments of Immunology and Medicine, and Institute of Medical Science, St. Marianna University School of Medicine, Kanagawa, Japan
ABSTRACT
Background
Fas/Fas ligand (FasL) system has been assigned a pivotal role in the development and maintenance of peripheral
tolerance, and mice with defects in their Fas/FasL system develop lupus-like symptoms. In this study we examined FasL expression of peripheral blood lymphocytes in patients with systemic lupus erythematosus
(SLE).
Methods
We assessed FasL mRNA and protein expression by reverse transcription (RT)-PCR and immunoblotting and immunocytochemical staining, respectively, in patients with SLE. Anti-DNA antibody secreting B cells were purified using biotin labeled DNA and streptavidin-bead.
Results
Expression of FasL protein was not or very weakly detected in freshly isolated PBMC in normal individuals. In
contrast, freshly isolated SLE PBMC exhibited the enhanced expression of FasL protein without in vitro stimulation. Not only purified T cells but also purified B cells expressed FasL on their cell surface spontaneously. In addition, freshly isolated anti-DNA autoantibody secreting B cells express FasL without in vitro stimulation.
Conclusion
The results suggest that autoreactive B lymphocytes which aberrantly express FasL may kill Fas+ immunoregulatory T lymphocytes. Thus aberrantly expressed FasL may facilitate escape of the autoreactive B cells from the immune
tolerance system, and may contribute to the sustained secretion of autoantibodies in patients with SLE.
Key words
Human, B lymphocytes, lupus, apoptosis.
Please address correspondence and reprint requests to: Dr. Noboru Suzuki, Departments of Immunology and Medicine, St. Marianna University School of Medicine, 2-16-1, Sugao, Miyamae-ku, Kawasaki, Kanagawa 216-8511, Japan.
E-mail: n3suzuki@marianna-u.ac.jp
Clin Exp Rheumatol 2002; 20: 625-631.
© Copyright Clinical and Experimental
Rheumatology 2002.