Wang C H, Richards E M, Block R D, Lezcano E M, Gutierrez R
Biology Department, California State University, 5500 University parkway, San Bernardino, CA 92407, USA.
Front Biosci. 1998 Nov 1;3:A58-65. doi: 10.2741/a253.
In this study, B lymphocytes from the small intestine of immunized rats were examined for their expression of specific antibodies against Trichinella spiralis (TS) antigen. The isotypes of the antigen-specific antibodies on B cells were examined via immunofluorescence microscopy. Monoclonal mouse anti-rat IgE, IgG1, IgG2a, IgG2b, IgG2c, IgA and IgM primary antibodies in conjunction with FITC-conjugated goat anti-mouse Ig secondary antibody and XRITC-conjugated 9D4 T. spiralis antigen were used to study the dynamics of the appearance of activated B lymphocytes in the small intestine, Peyer's patch, both the germinal center (PP-GC) and the non-germinal center (PP-NGC), the mesenteric lymph node (MLN), and the spleen. The results demonstrate that activated B cells are elicited by TS in the non-Peyer's patch region of the small intestine to express all isotypes of antibodies against TS antigen. IgG- and IgE-producing cells (Ab-PC) began proliferation only 1 and 2 days after infection, respectively. The strongest response was mounted by the IgE-PC in the lamina propria of the intestine. The response by IgA-PC generated was not only significantly delayed and also much weaker than that of the IgE- and IgG-PC. Peyer's patches failed to be a significant contributor in this immune response. Although this antigen-specific immune response was produced in the MLN and the spleen, it was weaker than that of the small intestine. The study indicates the potential ability of an immunized host to generate an early, yet effective, humoral immunity against T. spiralis in the non-Peyer's patch region of the small intestine."
在本研究中,检测了免疫大鼠小肠中的B淋巴细胞针对旋毛虫(TS)抗原的特异性抗体表达情况。通过免疫荧光显微镜检查B细胞上抗原特异性抗体的亚型。使用单克隆小鼠抗大鼠IgE、IgG1、IgG2a、IgG2b、IgG2c、IgA和IgM一抗,结合异硫氰酸荧光素(FITC)偶联的山羊抗小鼠Ig二抗以及异硫氰酸罗丹明(XRITC)偶联的9D4旋毛虫抗原,研究小肠、派伊尔结、生发中心(PP-GC)和非生发中心(PP-NGC)、肠系膜淋巴结(MLN)以及脾脏中活化B淋巴细胞出现的动态变化。结果表明,TS在小肠的非派伊尔结区域引发活化B细胞表达针对TS抗原的所有抗体亚型。产生IgG和IgE的细胞(抗体产生细胞,Ab-PC)分别在感染后仅1天和2天开始增殖。肠道固有层中的IgE-PC产生的反应最强。IgA-PC产生的反应不仅明显延迟,而且比IgE-PC和IgG-PC产生的反应弱得多。派伊尔结在这种免疫反应中并非主要贡献者。尽管在MLN和脾脏中产生了这种抗原特异性免疫反应,但比小肠中的要弱。该研究表明,免疫宿主在小肠的非派伊尔结区域具有针对旋毛虫产生早期且有效体液免疫的潜在能力。