James K, Hansen B, Gewurz H
J Immunol. 1981 Dec;127(6):2539-44.
Our laboratory previously reported that C-reactive protein (CRP) binds selectively to T lymphocytes and inhibits certain of their reactivities in vitro. However, these findings could not be repeated using more highly purified CRP preparations even under a variety of experimental conditions. Purified CRP alone did not bind to peripheral blood lymphocytes (PBL); however, in the presence of a ligand such as pneumococcal C-polysaccharide (CPS), CRP binding was readily detectable both by immunofluorescence and by a radioassay established for this purpose. The optimal concentration of CRP, ratio of CRP:CPS, and time and temperature for reactivity were determined using both assays. A markedly enhanced rate of binding was observed after pre-equilibration of CRP with calcium. A small percentage (mean 3.0%; range 0.5 to 8.0%) of PBL bound complexed CRP, and saturation was reached with 200 microgram CRP/ml. Reactivity of CRP with a multimeric form of phosphocholine (PC) (KLH-PC44) led to binding comparable to that observed with CPS, whereas monomeric PC inhibited the binding. Thus, in the presence of a multimeric binding specificity, CRP binds to a small fraction of peripheral blood lymphocytes, which are characterized in the accompanying paper.
我们实验室先前报道,C反应蛋白(CRP)可选择性地与T淋巴细胞结合,并在体外抑制其某些反应性。然而,即使在多种实验条件下,使用纯度更高的CRP制剂也无法重复这些发现。单独的纯化CRP不与外周血淋巴细胞(PBL)结合;然而,在诸如肺炎球菌C多糖(CPS)之类的配体存在下,通过免疫荧光和为此目的建立的放射测定法都能很容易地检测到CRP结合。使用这两种测定法确定了CRP的最佳浓度、CRP与CPS的比例以及反应的时间和温度。CRP与钙预平衡后,观察到结合速率明显提高。一小部分(平均3.0%;范围0.5%至8.0%)的PBL结合了复合CRP,200微克CRP/毫升时达到饱和。CRP与多聚体形式的磷酸胆碱(PC)(钥孔戚血蓝蛋白-PC44)的反应导致的结合与CPS观察到的结合相当,而单体PC则抑制结合。因此,在存在多聚体结合特异性的情况下,CRP与一小部分外周血淋巴细胞结合,这些淋巴细胞的特征在随附论文中进行了描述。