Li S, Maine G, Suzuki Y, Araujo F G, Galvan G, Remington J S, Parmley S
Department of Immunology, Research Institute, Palo Alto Medical Foundation, Palo Alto, California 94301, USA.
J Clin Microbiol. 2000 Jan;38(1):179-84. doi: 10.1128/JCM.38.1.179-184.2000.
A portion of a cDNA encoding a 35-kDa antigen from Toxoplasma gondii was cloned into the CKS expression vector and expressed in Escherichia coli. By using the enzyme-linked immunosorbent assay (ELISA), the recombinant protein (rP35 antigen) was examined for reactivity with immunoglobulin G (IgG) antibodies in the sera of pregnant women. Of these women, 41 had a toxoplasma serologic profile suggestive of recently acquired T. gondii infection (Sabin-Feldman dye test [DT] titers from 1:256 to 1:32,000, positive IgM ELISA titers from 2.3 to 9.7, positive IgA ELISA from 1 to >28, and acute patterns in the differential agglutination [AC/HS] test) (group I), and 50 women had a toxoplasma serologic profile suggestive of infection acquired in the distant past (low DT titers from 1:16 to 1:512, negative IgM ELISA titers from 0 to 0.8, and chronic patterns in the AC/HS test) (group II). The classification of acute or chronic profile was based on the individual's clinical history as well as the combination of the results of the toxoplasma serological profile. An additional group (group III) was composed of sera from 50 women who were seronegative for T. gondii antibodies in the DT. The results revealed that whereas 85.3% of women in group I had IgG antibodies that reacted with the rP35 antigen, only 8% of women in group II had IgG antibodies that reacted with the same antigen. In immunoblots, the rP35 antigen was recognized by IgG antibodies in a pool of sera from individuals with a toxoplasma serologic profile compatible with acute infection but not in a pool of sera from individuals with a serologic profile characteristic of a chronic infection. These results reveal that IgG antibodies against the P35 antigen are produced during the acute stage of the infection but are uncommon in the latent or chronic phase of the infection. Thus, the rP35 antigen may be a useful serologic marker to differentiate between recently acquired infection and that acquired in the more distant past.
将编码来自刚地弓形虫35 kDa抗原的部分cDNA克隆到CKS表达载体中,并在大肠杆菌中表达。通过酶联免疫吸附测定(ELISA),检测重组蛋白(rP35抗原)与孕妇血清中免疫球蛋白G(IgG)抗体的反应性。这些孕妇中,41人具有提示近期感染刚地弓形虫的弓形虫血清学特征(Sabin - Feldman染色试验[DT]效价从1:256至1:32,000,IgM ELISA阳性效价从2.3至9.7,IgA ELISA阳性从1至>28,以及差异凝集[AC/HS]试验中的急性模式)(第一组),50名妇女具有提示既往感染弓形虫的血清学特征(DT效价低,从1:16至1:512,IgM ELISA阴性效价从0至0.8,以及AC/HS试验中的慢性模式)(第二组)。急性或慢性特征的分类基于个体的临床病史以及弓形虫血清学特征结果的组合。另外一组(第三组)由50名在DT中弓形虫抗体血清学阴性的妇女的血清组成。结果显示,第一组中85.3%的妇女具有与rP35抗原反应的IgG抗体,而第二组中只有8%的妇女具有与相同抗原反应的IgG抗体。在免疫印迹中,rP35抗原在具有与急性感染相符的弓形虫血清学特征的个体血清池中被IgG抗体识别,但在具有慢性感染血清学特征的个体血清池中未被识别。这些结果表明,针对P35抗原的IgG抗体在感染急性期产生,但在感染的潜伏或慢性期不常见。因此,rP35抗原可能是区分近期获得的感染和既往获得的感染的有用血清学标志物。