Bone marrow CD34+ progenitor cells from rheumatoid arthritis patients support spontaneous transformation of peripheral blood B cells from healthy individuals

被引:0
作者
S. Hirohata
T. Yanagida
H. Nakamura
S. Yoshino
T. Tomita
T. Ochi
机构
[1] Department of Internal Medicine,
[2] Teikyo University School of Medicine,undefined
[3] 2-11-1 Kaga,undefined
[4] Itabashi-ku,undefined
[5] Tokyo 173-8605,undefined
[6] Japan e-mail: shunsei@med.teikyo-u.ac.jp Tel.: +81-3-3964-1211,undefined
[7] Ext. 1592; Fax: +81-3-3964-4707,undefined
[8] Department of Joint Disease and Rheumatism,undefined
[9] Nippon Medical School,undefined
[10] Tokyo,undefined
[11] Japan,undefined
[12] Department of Orthopedic Surgery,undefined
[13] Osaka University Medical School,undefined
[14] Osaka,undefined
[15] Japan,undefined
来源
Rheumatology International | 2000年 / 19卷
关键词
Key words Epstein-Barr virus; GM-CSF; Rheumatoid arthritis; Bone marrow; B cell activation;
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摘要
We show that bone marrow (BM) CD34+ progenitor cells from rheumatoid arthritis (RA) patients have the capacity to support spontaneous transformation of peripheral blood B cells. CD34+ cells purified from BM blood from eight RA patients and eight osteoarthritis (OA) patients were expanded with granulocyte/macrophage colony stimulating factor (GM-CSF) for 4–6 weeks. GM-CSF-stimulated BM CD34+ cells from three of eight RA patients, but none from seven OA patients, gave rise to spontaneous transformation of highly purified B cells of Epstein-Barr virus (EBV)- seronegative healthy donors. GM-CSF-stimulated BM CD34+ cells from four of six RA patients and from one of four OA patients also supported the spontaneous transformation of peripheral blood B cells from EBV-seropositive healthy donors. All the transformed B cell lines were positive for EBV-DNA as determined by PCR. Neither GM-CSF-stimulated BM CD34+ cells alone nor highly purified B cells alone gave rise to spontaneously transformed B cell lines. These results suggest that the capacity of BM CD34+ cells to support survival of B cells might contribute to the pathogenesis of RA by sustaining abnormal B cell responses.
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页码:153 / 159
页数:6
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