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通过抗体介导的免疫疗法治疗浆细胞异常增殖性疾病。

Treatment of plasma cell dyscrasias by antibody-mediated immunotherapy.

作者信息

Treon S P, Shima Y, Preffer F I, Doss D S, Ellman L, Schlossman R L, Grossbard M L, Belch A R, Pilarski L M, Anderson K C

机构信息

Division of Adult Oncology, Dana Farber Cancer Institute, Boston, MA 02115, USA.

出版信息

Semin Oncol. 1999 Oct;26(5 Suppl 14):97-106.

Abstract

The use of serotherapy to treat patients with plasma cell dyscrasias (PCDs) has been sought by us and others. Candidate antigens that have been targeted or proposed for targeting in PCDs include the immunoglobulin idiotype, CD19, CD38, CD54, CD126, HM1.24, and Muc-1 core protein. Unfortunately, many of these antigens are not ideal for use in serotherapy since they are not selectively expressed, are either shed or secreted, or have not been fully characterized. Serotherapy with an anti-CD19 monoclonal antibody (B4) conjugated to a blocked ricin toxin had no significant activity in patients with multiple myeloma (MM). Circulating CD20+ clonotypic B cells have been detected in the circulation of most MM and Waldenstrom's macroglobulinemia (WM) patients. Plasma cells from most WM patients express CD20, but most MM patient plasma cells either lack CD20 or express it weakly. In view of recent successes with anti-CD20-directed serotherapy in other B-cell malignancies, we initiated a phase II trial to study the anti-CD20 monoclonal antibody rituximab (Rituxan; IDEC Pharmaceuticals, San Diego, CA, and Genentech, Inc, San Francisco, CA) in patients with MM. We describe two PCD patients (one with WM and one with MM) who responded to therapy. By flow cytometric analysis, CD20+ plasma cells and B cells present in the bone marrow and peripheral blood of a patient with MM disappeared with response to rituximab therapy. However, residual CD20- tumor cells remained in the bone marrow following rituximab therapy, and after 6 months this patient progressed with CD20- myeloma cells. As a potential strategy to overcome this limitation, we demonstrated that interferon-gamma at pharmacologically achievable levels induced CD20 expression on these CD20- plasma cells, consistent with our recent findings that interferon-gamma is a potent inducer of CD20 expression on MM patient plasma cells and B cells. We also characterize a response to rituximab with a decrease in paraprotein and resolution of anemia in a patient with WM whose response to rituximab is ongoing after 19+ months. This preliminary experience supports the potential use of serotherapy targeting CD20 in PCDs. Our studies further suggest that interferon-gamma may enhance CD20 expression on MM plasma cells, thereby increasing their susceptibility to anti-CD20 monoclonal antibody therapies.

摘要

我们和其他研究人员一直在探索使用血清疗法治疗浆细胞异常增殖症(PCD)患者。在PCD中已被靶向或提议靶向的候选抗原包括免疫球蛋白独特型、CD19、CD38、CD54、CD126、HM1.24和Muc-1核心蛋白。不幸的是,这些抗原中的许多并不适合用于血清疗法,因为它们不是选择性表达,要么会脱落或分泌,要么尚未得到充分表征。用与封闭的蓖麻毒素偶联的抗CD19单克隆抗体(B4)进行血清疗法,在多发性骨髓瘤(MM)患者中没有显著活性。在大多数MM和华氏巨球蛋白血症(WM)患者的循环中检测到循环CD20+克隆型B细胞。大多数WM患者的浆细胞表达CD20,但大多数MM患者的浆细胞要么缺乏CD20,要么表达较弱。鉴于抗CD20导向的血清疗法在其他B细胞恶性肿瘤中最近取得的成功,我们启动了一项II期试验,研究抗CD20单克隆抗体利妥昔单抗(美罗华;IDEC制药公司,加利福尼亚州圣地亚哥,以及基因泰克公司,加利福尼亚州旧金山)在MM患者中的应用。我们描述了两名对治疗有反应的PCD患者(一名WM患者和一名MM患者)。通过流式细胞术分析,一名MM患者骨髓和外周血中的CD20+浆细胞和B细胞在对利妥昔单抗治疗有反应时消失。然而,利妥昔单抗治疗后骨髓中仍残留CD20-肿瘤细胞,6个月后该患者出现CD20-骨髓瘤细胞进展。作为克服这一局限性的潜在策略,我们证明在药理学可达到的水平下,干扰素-γ可诱导这些CD20-浆细胞表达CD20,这与我们最近的发现一致,即干扰素-γ是MM患者浆细胞和B细胞上CD20表达的有效诱导剂。我们还描述了一名WM患者对利妥昔单抗的反应,其副蛋白减少且贫血症状缓解,该患者在19个多月后仍在持续对利妥昔单抗有反应。这一初步经验支持了在PCD中使用靶向CD20的血清疗法的可能性。我们的研究进一步表明,干扰素-γ可能增强MM浆细胞上CD20的表达,从而增加它们对抗CD20单克隆抗体疗法的敏感性。

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