Zeman Alenka M, Holmes Tyson H, Stamatis Shaye, Tu Wenwei, He Xiao-Song, Bouvier Nancy, Kemble George, Greenberg Harry B, Lewis David B, Arvin Ann M, Dekker Cornelia L
Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305-5208, USA.
Pediatr Infect Dis J. 2007 Feb;26(2):107-15. doi: 10.1097/01.inf.0000253251.03785.9b.
There have been no prior reports of the frequency of circulating influenza-specific, interferon gamma-producing memory CD4+ and CD8+ T-cells in healthy children who have received multiple influenza immunizations.
We evaluated 21 previously immunized children, ages 3 to 9 years, before and 1 month after administration of trivalent inactivated influenza vaccine. Frequencies of influenza-specific CD4+ and CD8+ T-cells stimulated with trivalent inactivated influenza vaccine or A/Panama (H3N2) virus were determined by flow cytometry, and antibody responses to vaccine strains and a drifted H3N2 strain were measured by hemagglutination inhibition assay and neutralizing antibody assays.
Mean change in CD4+ and in CD8+ T-cell frequencies after immunization was 0.01% (P > 0.39) with postimmunization CD4+ frequencies higher than CD8+ frequencies. Children with more previous vaccinations had a higher baseline frequency of CD4+ T-cells (P = 0.0002) but a smaller increase or even a decline from baseline after immunization (P = 0.003). An association between age and change in frequency was not detected. Baseline geometric mean titers (GMTs) and seroprotection rates were significantly higher in older children against A/Panama (neutralizing baseline GMT, P = 0.0488) and A/New Caledonia (hemagglutination inhibition baseline GMT and seroprotection, P < 0.0297). Baseline GMTs against B/Hong Kong were not associated with age or quantity of prior vaccinations.
These findings suggest that children may plateau in CD4+ T-cell responses to influenza antigens with repeated exposures and that the number of exposures may play a large role in building a memory CD4+ T-cell response to influenza A, perhaps independently from age.
此前尚无关于多次接种流感疫苗的健康儿童中循环流感特异性、产生干扰素γ的记忆性CD4+和CD8+T细胞频率的报道。
我们评估了21名年龄在3至9岁之间、之前已接种过疫苗的儿童,在接种三价灭活流感疫苗之前和之后1个月进行评估。通过流式细胞术确定用三价灭活流感疫苗或A/巴拿马(H3N2)病毒刺激后的流感特异性CD4+和CD8+T细胞频率,并通过血凝抑制试验和中和抗体试验测量对疫苗株和一株发生抗原漂移的H3N2毒株的抗体反应。
免疫后CD4+和CD8+T细胞频率的平均变化为0.01%(P>0.39),免疫后CD4+频率高于CD8+频率。之前接种次数较多的儿童CD4+T细胞的基线频率较高(P = 0.0002),但免疫后较基线的增加较小甚至下降(P = 0.003)。未检测到年龄与频率变化之间的关联。年龄较大的儿童针对A/巴拿马(中和基线几何平均滴度,P = 0.0488)和A/新喀里多尼亚(血凝抑制基线几何平均滴度和血清保护率,P<0.0297)的基线几何平均滴度(GMT)和血清保护率显著更高。针对B/香港的基线GMT与年龄或之前接种的次数无关。
这些发现表明,儿童在反复接触流感抗原后,其CD4+T细胞对流感抗原的反应可能会达到平台期,并且接触次数可能在建立对甲型流感的记忆性CD4+T细胞反应中起很大作用,这可能独立于年龄因素。