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生发中心发育早期的抗体形成细胞诱导及其随衰老的延迟。

Antibody-forming cell induction during an early phase of germinal centre development and its delay with ageing.

作者信息

Kosco M H, Burton G F, Kapasi Z F, Szakal A K, Tew J G

机构信息

Department of Microbiology and Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond.

出版信息

Immunology. 1989 Nov;68(3):312-8.

Abstract

The present study was initiated to determine if an early phase of germinal centre (GC) development is associated with the generation of antibody-forming cells (AFC). Germinal centres in draining lymph nodes from immune mice were examined histochemically after secondary immunization for the presence of AFC at both the light and electron microscopic levels. Additionally, peanut agglutinin (PNA) high (Hi) GC B cells were isolated, placed in cell culture and specific antibody production was monitored at successive intervals. Electron microscopy showed that plasma cells in all stages of differentiation were present within GC at 3-5 days and to a lesser extent at 7 days following antigenic challenge. Furthermore, PNAHi GC B cells obtained between Days 3 and 5 spontaneously produced specific IgG when placed in culture. Germinal centre B cells isolated either before or after this period did not produce antibody without the addition of T-cell cytokines. Induction of AFC in GC occurred at the time when GC B cells acquire follicular dendritic cell (FDC)-derived, immune complex-coated bodies (iccosomes) and process and present this antigen to helper T cells. This suggested a causal relationship between iccosome release and AFC induction. Support for this was obtained by examination of AFC induction in aged mice where iccosome release has not been observed. Peanut agglutinin-positive GC B cells isolated from aged mice on Days 3-5 after antigen challenge failed to spontaneously produce specific antibody. Collectively, these data show that GC development 3-5 days after booster immunization results in AFC generation and suggests a role for FDC iccosomes in their induction.

摘要

本研究旨在确定生发中心(GC)发育的早期阶段是否与抗体形成细胞(AFC)的产生有关。在二次免疫后,对免疫小鼠引流淋巴结中的生发中心进行组织化学检查,在光学和电子显微镜水平检测AFC的存在。此外,分离出花生凝集素(PNA)高表达(Hi)的GC B细胞,置于细胞培养中,并在连续的时间间隔监测特异性抗体的产生。电子显微镜显示,在抗原攻击后3 - 5天,GC内存在各个分化阶段的浆细胞,7天时数量较少。此外,在第3天至第5天获得的PNAHi GC B细胞在培养时自发产生特异性IgG。在此期间之前或之后分离的GC B细胞在不添加T细胞细胞因子的情况下不产生抗体。GC中AFC的诱导发生在GC B细胞获得滤泡树突状细胞(FDC)衍生的免疫复合物包被小体(iccosomes)并处理该抗原并将其呈递给辅助性T细胞的时候。这表明iccosome释放与AFC诱导之间存在因果关系。通过检查未观察到iccosome释放的老年小鼠中的AFC诱导获得了对此的支持。从抗原攻击后第3 - 5天的老年小鼠中分离的花生凝集素阳性GC B细胞未能自发产生特异性抗体。总体而言,这些数据表明加强免疫后3 - 5天的GC发育导致AFC产生,并提示FDC iccosomes在其诱导中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0a3/1385441/d16fb2d18737/immunology00138-0023-a.jpg

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