Pakkanen S H, Kantele J M, Rombo L, Kantele A
Department of Bacteriology and Immunology, University of Helsinki, Helsinki, Finland.
Occupational Health and Environmental Medicine, Department of Public Health, University of Turku, Turku, Finland.
Scand J Immunol. 2017 Oct;86(4):207-215. doi: 10.1111/sji.12583.
Secondary immunization with polysaccharide vaccines may imply a risk of hyporesponsiveness. Despite the wide use of typhoid Vi capsular polysaccharide vaccine, its potential tendency to hyporesponsiveness has been inadequately addressed. While previous studies have explored serum antibody responses, we applied a more sensitive approach, a single-cell assay for circulating plasmablasts, to compare primary and secondary responses. Twelve subjects received primary and booster doses of the Vi vaccine (Typherix ) at 30- to 37-month intervals. Plasmablasts specific to the Vi or typhoidal O antigens or cross-reactive with paratyphoid and non-typhoidal Salmonella strains were identified as antibody-secreting cells (ASC) with ELISPOT. Before vaccinations, none had plasmablasts specific to the antigens tested. Twelve of 12 subjects showed a Vi-specific response after primary, but only eight of 12 after booster vaccination. All responded to typhoidal O-9,12 antigen after both immunizations. The geometric mean of plasmablasts specific to the Vi antigen was 59 (95% CI 24-119) and 1 (0-54) IgA + IgG + IgM-ASC/10 peripheral blood mononuclear cell (PBMC) after primary and booster immunizations, respectively, and 20 (9-49) and 56 (29-103) to the O-9,12 antigen. We detected 1 (0-28) and 17 (6-36) ASC/10 PBMC cross-reactive with Salmonella Paratyphi A; 3 (0-30) and 22 (8-48) with S. Paratyphi B; 3 (0-29) and 18 (7-47) with S. Paratyphi C; 19 (10-34) and 51 (26-94) with Salmonella Enteritidis; and 1 (0-35) and 23 (9-52) with Salmonella Typhimurium, respectively. One-third of the vaccinees, although responding to the O-9,12 antigen, failed to respond to the Vi antigen after booster immunization, suggesting hyporesponsiveness in part of the vaccinees. The findings warrant further investigation.
用多糖疫苗进行二次免疫可能意味着存在低反应性风险。尽管伤寒Vi荚膜多糖疫苗被广泛使用,但其潜在的低反应性倾向尚未得到充分研究。虽然先前的研究探讨了血清抗体反应,但我们采用了一种更敏感的方法,即循环浆母细胞单细胞检测法,来比较初次和二次反应。12名受试者每隔30至37个月接受一次Vi疫苗(Typherix)的初次和加强剂量接种。通过酶联免疫斑点法(ELISPOT)将对Vi或伤寒O抗原特异或与副伤寒和非伤寒沙门氏菌菌株交叉反应的浆母细胞鉴定为抗体分泌细胞(ASC)。接种疫苗前,无人有针对所测抗原的浆母细胞。12名受试者中有12名在初次接种后出现了Vi特异性反应,但在加强接种后只有8名出现反应。两次免疫后,所有人均对伤寒O-9,12抗原产生反应。初次和加强免疫后,针对Vi抗原的浆母细胞几何平均值分别为59(95%CI 24 - 119)和1(0 - 54)个IgA + IgG + IgM-ASC/10外周血单个核细胞(PBMC),针对O-9,12抗原的分别为20(9 - 49)和56(29 - 103)个。我们检测到每10个PBMC中与甲型副伤寒沙门氏菌交叉反应的ASC分别为1(0 - 28)和17(6 - 36)个;与乙型副伤寒沙门氏菌交叉反应的分别为3(0 - 30)和22(8 - 48)个;与丙型副伤寒沙门氏菌交叉反应的分别为3(0 - 29)和18(7 - 47)个;与肠炎沙门氏菌交叉反应的分别为19(10 - 34)和51(26 - 94)个;与鼠伤寒沙门氏菌交叉反应的分别为1(0 - 35)和23(9 - 52)个。三分之一的疫苗接种者尽管对O-9,12抗原产生反应,但在加强免疫后对Vi抗原无反应,提示部分疫苗接种者存在低反应性。这些发现值得进一步研究。