Montes Carolina L, Acosta-Rodríguez Eva V, Merino Maria Cecilia, Bermejo Daniela A, Gruppi Adriana
Department of Clinical Biochemistry, School of Chemical Science, National University of Córdoba, Córdoba, Argentina.
J Leukoc Biol. 2007 Nov;82(5):1027-32. doi: 10.1189/jlb.0407214. Epub 2007 Jul 5.
Polyclonal B cell activation is not a peculiar characteristic to a particular infection, as many viruses, bacteria, and parasites induce a strong polyclonal B cell response resulting in hyper-gamma-globulinemia. Here, we discuss the different roles proposed for polyclonal B cell activation, which can be crucial for early host defense against rapidly dividing microorganisms by contributing antibodies specific for a spectrum of conserved structures present in the pathogens. In addition, polyclonal B cell activation can be responsible for maintenance of memory B cell responses because of the continuous, unrestricted stimulation of memory B cells whose antibody production may be sustained in the absence of the antigens binding-specific BCR. Conversely, polyclonal activation can be triggered by microorganisms to avoid the host-specific, immune response by activating B cell clones, which produce nonmicroorganism-specific antibodies. Finally, some reports suggest a deleterious role for polyclonal activation, arguing that it could potentially turn on anti-self-responses and lead to autoimmune manifestations during chronic infections.
多克隆B细胞激活并非特定感染所特有的特征,因为许多病毒、细菌和寄生虫都会诱导强烈的多克隆B细胞反应,导致高γ球蛋白血症。在此,我们讨论了多克隆B细胞激活所发挥的不同作用,这对于宿主早期抵御快速分裂的微生物可能至关重要,因为它能产生针对病原体中一系列保守结构的特异性抗体。此外,多克隆B细胞激活可能负责记忆B细胞反应的维持,这是由于记忆B细胞受到持续、无限制的刺激,其抗体产生在没有抗原结合特异性BCR的情况下仍可持续。相反,微生物可通过激活产生非微生物特异性抗体的B细胞克隆来触发多克隆激活,从而避免宿主特异性免疫反应。最后,一些报告表明多克隆激活具有有害作用,认为它可能在慢性感染期间引发自身反应并导致自身免疫表现。