Le Thuan, Cherry James D, Chang Swei-Ju, Knoll Maria Deloria, Lee Martin L, Barenkamp Steve, Bernstein David, Edelman Robert, Edwards Kathryn M, Greenberg David, Keitel Wendy, Treanor John, Ward Joel I
UCLA Center for Vaccine Research, Research and Education Institute, Harbor-UCLA Medical Center, UCLA School of Medicine, Torrance 90502, USA.
J Infect Dis. 2004 Aug 1;190(3):535-44. doi: 10.1086/422035. Epub 2004 Jul 7.
As part of a prospective acellular pertussis (ACP) vaccine efficacy trial, 5 serum samples were obtained, over an 18-month period, from 101 ACP-vaccine recipients and 99 control subjects, to assess ACP antibody response and decay. Immunoglobulin (Ig) G and IgA antibodies to pertussis toxin (PT), filamentous hemagglutinin (FHA), pertactin (PRN), and fimbriae 2/3 (FIM) were measured by enzyme-linked immunosorbant assay, and titers of agglutinin were determined. Of the subjects, 16%-19% had preimmunization values of antibodies to PT that were above the assay's limit of quantitation (LOQ); in contrast, 36%-63% of the subjects had preimmunization values of antibodies to FHA, PRN, or FIM that were above the LOQ. Substantial increases in titers of IgG and IgA antibodies to the 3 ACP antigens (PT, FHA, and PRN) were observed. Over the 18-months, the percent decay in IgG and IgA antibodies ranged from 56% to 73% and from 57% to 70%, respectively; the IgG antibody response and decay suggests that geometric mean titers likely remain above the LOQ for 2-9 years and above the threshold of detection for 4-13 years. These findings support the use of ACP booster immunizations for adolescents and adults, to provide sustained levels of antibody.
作为一项前瞻性无细胞百日咳(ACP)疫苗效力试验的一部分,在18个月期间从101名接种ACP疫苗者和99名对照受试者中获取了5份血清样本,以评估ACP抗体反应和衰减情况。通过酶联免疫吸附测定法测量了针对百日咳毒素(PT)、丝状血凝素(FHA)、百日咳杆菌黏附素(PRN)和2/3型菌毛(FIM)的免疫球蛋白(Ig)G和IgA抗体,并测定了凝集素滴度。在这些受试者中,16% - 19%的人PT抗体的免疫前值高于检测方法的定量下限(LOQ);相比之下,36% - 63%的受试者FHA、PRN或FIM抗体的免疫前值高于LOQ。观察到针对3种ACP抗原(PT、FHA和PRN)的IgG和IgA抗体滴度大幅增加。在18个月期间,IgG和IgA抗体的衰减百分比分别为56%至73%和57%至70%;IgG抗体反应和衰减表明几何平均滴度可能在2至9年保持高于LOQ,在4至13年保持高于检测阈值。这些发现支持对青少年和成人使用ACP加强免疫,以提供持续的抗体水平。