Granato Alessandra, Chen Yuezhou, Wesemann Duane R
Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Curr Opin Immunol. 2015 Apr;33:126-31. doi: 10.1016/j.coi.2015.02.011. Epub 2015 Mar 19.
The primary immunoglobulin repertoire develops via opposing forces of expanding diversification balanced by contracting selection mechanisms. The resulting shape is essential for host health and immune fitness. While the molecular mechanisms of Ig diversification have largely been defined, selection forces shaping emerging Ig repertoires are poorly understood. During lifetime, human and mouse early B cell development occurs at distinct locations-beginning in fetal liver before transferring to bone marrow and spleen by the end of gestation. During an early life window of time, the murine gut lamina propria harbors developing immature B cells in proximity to intestinal contents such as commensal microbes and dietary antigens. Location and timing of early B cell development may thus endow neighboring antigens with primary repertoire-shaping capabilities.
初始免疫球蛋白库通过扩张多样化的对抗力量与收缩选择机制相平衡而形成。其最终形态对宿主健康和免疫适应性至关重要。虽然免疫球蛋白多样化的分子机制已基本明确,但塑造新出现的免疫球蛋白库的选择力量却知之甚少。在整个生命周期中,人类和小鼠的早期B细胞发育发生在不同的位置——始于胎儿肝脏,在妊娠末期转移至骨髓和脾脏。在生命早期的一段时间内,小鼠肠道固有层中存在发育中的未成熟B细胞,它们靠近肠道内容物,如共生微生物和饮食抗原。因此,早期B细胞发育的位置和时间可能赋予邻近抗原塑造初始库的能力。