Yu Esther Dawen, Grifoni Alba, Sutherland Aaron, Voic Hannah, Wang Eric, Frazier April, Jimenez-Truque Natalia, Yoder Sandra, Welsh Sabrina, Wooden Stacey, Koff Wayne, Creech Buddy, Sette Alessandro, da Silva Antunes Ricardo
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, CA 92037, USA.
Vanderbilt Vaccine Research Program, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Vaccines (Basel). 2021 Apr 23;9(5):426. doi: 10.3390/vaccines9050426.
The role of T cell immunity has been acknowledged in recent vaccine development and evaluation. We tested the humoral and cellular immune responses to Flucelvax, a quadrivalent inactivated seasonal influenza vaccine containing two influenza A (H1N1 Singapore/GP1908/2015 IVR-180 and H3N2 North Carolina/04/2016) and two influenza B (Iowa/06/2017 and Singapore/INFTT-16-0610/2016) virus strains, using peripheral blood mononuclear cells stimulated by pools of peptides overlapping all the individual influenza viral protein components. Baseline reactivity was detected against all four strains both at the level of CD4 and CD8 responses and targeting different proteins. CD4 T cell reactivity was mostly directed to HA/NA proteins in influenza B strains, and NP/M1/M2/NS1/NEP proteins in the case of the Influenza A strains. CD8 responses to both influenza A and B viruses preferentially targeted the more conserved core viral proteins. Following vaccination, both CD4 and CD8 responses against the various influenza antigens were increased in day 15 to day 91 post vaccination period, and maintained a Th1 polarized profile. Importantly, no vaccine interference was detected, with the increased responses balanced across all four included viral strains for both CD4 and CD8 T cells, and targeting HA and multiple additional viral antigens.
T细胞免疫在近期疫苗研发和评估中的作用已得到认可。我们使用外周血单核细胞,通过与所有单个流感病毒蛋白成分重叠的肽池刺激,测试了对Flucelvax(一种四价灭活季节性流感疫苗,包含两种甲型流感病毒株(H1N1新加坡/GP1908/2015 IVR - 180和H3N2北卡罗来纳/04/2016)以及两种乙型流感病毒株(爱荷华/06/2017和新加坡/INFTT - 16 - 0610/2016))的体液免疫和细胞免疫反应。在CD4和CD8反应水平以及针对不同蛋白质方面,均检测到对所有四种病毒株的基线反应性。CD4 T细胞反应性在乙型流感病毒株中主要针对HA/NA蛋白,在甲型流感病毒株中则针对NP/M1/M2/NS1/NEP蛋白。对甲型和乙型流感病毒的CD8反应均优先靶向更保守的核心病毒蛋白。接种疫苗后,在接种后第15天至第91天期间,针对各种流感抗原的CD4和CD8反应均增强,并维持Th1极化状态。重要的是,未检测到疫苗干扰,CD4和CD8 T细胞对所有四种纳入病毒株的反应性增加且平衡,同时针对HA和多种其他病毒抗原。