Department of Obstetrics and Gynecology, Hôpital Foch, 92120 Suresnes, France; Risk in Pregnancy University Department, IAME, INSERM, Université Paris-Diderot, 75013 Paris, France; Groupe de Recherche sur les Infections pendant la Grossesse (GRIG), France.
Groupe de Recherche sur les Infections pendant la Grossesse (GRIG), France; AP-HP, Hôpital Paul Brousse, Department of Virology, WHO Rubella NRL, 94804 Villejuif, France.
J Clin Virol. 2019 Mar;112:27-33. doi: 10.1016/j.jcv.2019.01.009. Epub 2019 Jan 24.
Immunity to rubella-virus (RV) is commonly determined by measuring specific IgG (RV-IgG). However, RV-IgG results may be different and even discordant, depending on the assay used. Cell-mediated immunity is not routinely investigated for diagnostic purposes.
Our aim was to investigate humoral and cellular immunity of women with negative or equivocal RV-IgG before, and after post-partum vaccination.
A total of 186 pregnant women were included in the study. During pregnancy, humoral immunity was investigated with two RV-IgG immunoassays, an immunoblot and a T-cell mediated immunity test. In the post-partum vaccination period, measuring RV-IgM and RV-IgG avidity allowed us to determine whether women raised a primary or a secondary immune response.
Before vaccination, 52.2% women, supposed to be susceptible, had positive anti-E1 RV-IgG indicating strong evidence of previous exposure to RV. All (100%) pregant women who had a positive immunoblot before immunization raised a secondary immune response to vaccination, and 96.8% who had a negative immunoblot before immunization, raised a primary immune response to vaccination. All women who raised a primary immune response after vaccination had negative anti-E1 RV-IgG and negative cell-mediated immunity.
These results indicate that individuals can have evidence of protective immunity against rubella despite negative RV-IgG.
风疹病毒 (RV) 免疫力通常通过测量特异性 IgG (RV-IgG) 来确定。然而,由于检测方法的不同,RV-IgG 结果可能存在差异,甚至不一致。细胞介导的免疫通常不用于诊断目的。
我们的目的是研究阴性或可疑 RV-IgG 的女性在产后接种前后的体液和细胞免疫情况。
共有 186 名孕妇纳入本研究。在怀孕期间,通过两种 RV-IgG 免疫测定法、免疫印迹和 T 细胞介导的免疫测试来研究体液免疫。在产后疫苗接种期间,测量 RV-IgM 和 RV-IgG 亲和力可以确定女性产生的是原发性免疫反应还是次级免疫反应。
在接种疫苗前,52.2% 被认为易感染的女性具有抗 E1 RV-IgG 阳性,表明其以前曾接触过 RV,这是强烈的证据。所有(100%)在免疫前免疫印迹阳性的孕妇在接种疫苗后均产生了次级免疫反应,而在免疫前免疫印迹阴性的孕妇中,有 96.8% 产生了初级免疫反应。所有在接种疫苗后产生初级免疫反应的女性的抗 E1 RV-IgG 和细胞介导免疫均为阴性。
这些结果表明,尽管 RV-IgG 阴性,但个体可能具有针对风疹的保护性免疫证据。