a Department of Clinical Science; University of Bergen; Bergen, Norway.
Hum Vaccin Immunother. 2014;10(8):2408-16. doi: 10.4161/hv.29583.
T cellular responses play a significant role in mediating protective immune responses against influenza in humans. In the current study, we evaluated the ability of a candidate virosomal H5N1 vaccine adjuvanted with Matrix M(TM) to induce CD4(+) and CD8(+) T cell responses in a phase 1 clinical trial. We vaccinated 60 healthy adult volunteers (at days 0 and 21) with 30 μg haemagglutinin (HA) alone or 1.5, 7.5, or 30 μg HA formulated with Matrix M(TM). To evaluate the T cellular responses, lymphocytes were stimulated in vitro with homologous (A/Vietnam/1194/2004 [H5N1]) and heterologous H5N1 (A/Anhui/1/05 or A/Bar-headed Goose/Qinghai/1A/05) antigens. The antigen-specific cytokine responses were measured by intracellular cytokine staining and by multiplex (Luminex) assays. An increase in CD4(+) Th1 and Th2 cytokines was detected 21 days after the first vaccine dose. No increase in Th cytokine responses was observed after the second dose, although it is possible that the cytokine levels peaked earlier than sampling point at day 42. Formulation with the Matrix M(TM) adjuvant augmented both the homologous and cross-reactive cytokine response. Antigen-specific CD8(+) T cell responses were detected only in a few vaccinated individuals. The concentrations of Th1 and to a lesser extent, Th2 cytokines at 21 days post-vaccination correlated moderately with subsequent days 35 and 180 serological responses as measured by the microneutralisation, haemagglutination inhibition, and single radial hemolysis assays. Results presented here show that the virosomal H5N1 vaccine induced balanced Th1/Th2 cytokine responses and that Matrix M(TM) is a promising adjuvant for future development of candidate pandemic influenza vaccines.
T 细胞反应在介导人体对流感的保护性免疫反应中发挥着重要作用。在目前的研究中,我们评估了一种候选的 H5N1 病毒样颗粒疫苗与 Matrix M(TM)佐剂联合使用在人体中诱导 CD4(+)和 CD8(+)T 细胞反应的能力。我们在第 0 天和第 21 天给 60 名健康成年志愿者接种 30 μg 血凝素(HA),单独接种或与 Matrix M(TM)联合接种 1.5、7.5 或 30 μg HA。为了评估 T 细胞反应,我们将淋巴细胞在体外与同源(A/Vietnam/1194/2004 [H5N1])和异源 H5N1(A/Anhui/1/05 或 A/Bar-headed Goose/Qinghai/1A/05)抗原刺激。通过细胞内细胞因子染色和多重(Luminex)检测来测量抗原特异性细胞因子反应。在第一次疫苗接种后 21 天,检测到 CD4(+)Th1 和 Th2 细胞因子增加。第二次接种后未观察到 Th 细胞因子反应增加,尽管可能在第 42 天的采样点之前细胞因子水平已经达到峰值。用 Matrix M(TM)佐剂进行制剂增强了同源和交叉反应性细胞因子反应。仅在少数接种个体中检测到抗原特异性 CD8(+)T 细胞反应。接种后 21 天 Th1 和(在较小程度上)Th2 细胞因子的浓度与随后的第 35 天和第 180 天的血清学反应(通过微量中和、血凝抑制和单径向溶血测定测量)中度相关。这里呈现的结果表明,病毒样颗粒 H5N1 疫苗诱导了平衡的 Th1/Th2 细胞因子反应,Matrix M(TM)是未来开发候选大流行性流感疫苗的有前途的佐剂。