抗原
免疫学
生物
免疫系统
约氏疟原虫
抗体
卵清蛋白
佐剂
T细胞
CD40
B细胞
体液免疫
细胞毒性T细胞
生物化学
恶性疟原虫
体外
寄生虫血症
疟疾
作者
Silvia Beatriz Boscardin,Julius Clemence R. Hafalla,Revati F. Masilamani,Alice O. Kamphorst,Henry Zebroski,Urvashi Rai,Alexandre Morrot,Fidel Zavala,Ralph M. Steinman,Ruth S. Nussenzweig,Michel C. Nussenzweig
摘要
Resistance to several prevalent infectious diseases requires both cellular and humoral immune responses. T cell immunity is initiated by mature dendritic cells (DCs) in lymphoid organs, whereas humoral responses to most antigens require further collaboration between primed, antigen-specific helper T cells and naive or memory B cells. To determine whether antigens delivered to DCs in lymphoid organs induce T cell help for antibody responses, we targeted a carrier protein, ovalbumin (OVA), to DCs in the presence of a maturation stimulus and assayed for antibodies to a hapten, (4-hydroxy-3-nitrophenyl) acetyl (NP), after boosting with OVA-NP. A single DC-targeted immunization elicited long-lived T cell helper responses to the carrier protein, leading to large numbers of antibody-secreting cells and high titers of high-affinity antihapten immunoglobulin Gs. Small doses of DC-targeted OVA induced higher titers and a broader spectrum of anti-NP antibody isotypes than large doses of OVA in alum adjuvant. Similar results were obtained when the circumsporozoite protein of Plasmodium yoelii was delivered to DCs. We conclude that antigen targeting to DCs combined with a maturation stimulus produces broad-based and long-lived T cell help for humoral immune responses.
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