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华氏巨球蛋白血症中的自身抗体活性。

Autoantibody activity in Waldenstrom's macroglobulinemia.

作者信息

Stone Marvin J, Merlini Giampaolo, Pascual Virginia

机构信息

Baylor Charles A. Sammons Cancer Center, 3535 Worth Street, Dallas, TX 75246, USA.

出版信息

Clin Lymphoma. 2005 Mar;5(4):225-9. doi: 10.3816/clm.2005.n.004.

Abstract

Some monoclonal proteins from patients with Waldenstrom's macroglobulinemia (WM) or immunoglobulin (Ig) M monoclonal gammopathy of undetermined significance possess antigen-binding activity directed to autogenous or foreign antigens. These monoclonal IgM autoantibodies include cold agglutinins, mixed cryoglobulins, and antineural components. Because of the antigenantibody interaction, patients with these autoimmune syndromes often present with hemolytic anemia, mixed cryoglobulinemia, or peripheral neuropathy, respectively, at an earlier stage than patients with typical WM who do not have evident antibody activity. The presence of monoclonal macroglobulin autoreactive antibodies thus influences clinical presentation and natural history. Monoclonal IgM antibodies display polyreactivity to antigens of microbial origin in addition to autogenous antigens and may arise through T-independent as well as T-dependent pathways. Waldenstrom proteins with antibody activity appear to provide a link between autoimmunity, infection, and lymphoproliferative disease. Study of the antigens reacting with monoclonal IgMs may provide further insight into the pathogenesis of WM.

摘要

一些来自华氏巨球蛋白血症(WM)患者或意义未明的免疫球蛋白(Ig)M单克隆丙种球蛋白病患者的单克隆蛋白具有针对自身或外来抗原的抗原结合活性。这些单克隆IgM自身抗体包括冷凝集素、混合冷球蛋白和抗神经成分。由于抗原-抗体相互作用,与没有明显抗体活性的典型WM患者相比,患有这些自身免疫综合征的患者通常分别在更早阶段出现溶血性贫血、混合冷球蛋白血症或周围神经病变。因此,单克隆巨球蛋白自身反应性抗体的存在会影响临床表现和自然病程。单克隆IgM抗体除了对自身抗原外,还对微生物来源的抗原表现出多反应性,并且可能通过非T细胞依赖性以及T细胞依赖性途径产生。具有抗体活性的华氏巨球蛋白似乎在自身免疫、感染和淋巴增殖性疾病之间提供了一种联系。研究与单克隆IgM反应的抗原可能会为WM的发病机制提供进一步的见解。

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