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This article was retracted on October 15, 2008.
Blood, 1 July 2004, Vol. 104, No. 1, pp. 184-191.
Prepublished online as a Blood First Edition Paper on March 4, 2004; DOI 10.1182/blood-2003-12-4274.

Submitted December 17, 2003
Accepted February 25, 2004
TNF related apoptosis inducing ligand is involved in neutropenia of systemic lupus erythematosus
Wataru Matsuyama*, Masuki Yamamoto, Ikkou Higashimoto, Ken-ichi Oonakahara, Masaki Watanabe, Kentarou Machida, Teizo Yoshimura, Nobutaka Eiraku, Masaharu Kawabata, Mitsuhiro Osame, and Kimiyoshi Arimura
Third Department of Internal Medicine, Kagoshima University Faculty of Medicine, Kagoshima, Japan
Laboratory of Molecular Immunoregulation, National Cancer Institute-Frederick, Frederick, MD, USA
Department of Respiratory Medicine, National Minami-kyushu Hospital, Kagoshima, Japan
* Corresponding author; email: vega{at}xa2.so-net.ne.jp.
Neutropenia is a common laboratory finding in systemic lupus erythematosus (SLE). However, the molecular mechanism of SLE neutropenia has not been fully explained. In this study, we examined whether TNF related apoptosis inducing ligand (TRAIL) is involved in the pathogenesis of SLE neutropenia using samples from SLE patients. Serum TRAIL levels in SLE patients with neutropenia were significantly higher than those of either SLE patients without neutropenia and healthy volunteers. Serum TRAIL levels showed a significant negative correlation with neutrophil counts in SLE patients. The expression of TRAIL receptor 3 was significantly lower in SLE patients with neutropenia than in either patients without neutropenia and healthy volunteers. Treatment with glucocorticoids negated the decrease of TRAIL receptor 3 expression on neutrophils of SLE patients. TRAIL may accelerate neutrophil apoptosis of neutrophils from SLE patients and autologous T-cells of SLE patients, which express TRAIL on surface, may kill autologous neutrophils. Interferon gamma and glucocorticoid modulated the expression of TRAIL on T cells of SLE patients and also modulated the expression of cellular FLICE-inhibitory protein (cFLIP), an inhibitor of death receptor signaling, in neutrophils. Thus, our results provide a novel insight in the molecular pathogenesis of SLE neutropenia.

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