Antigen targeting to dendritic cells elicits long-lived T cell help for antibody responses

Author:

Boscardin Silvia B.1,Hafalla Julius C.R.2,Masilamani Revati F.1,Kamphorst Alice O.1,Zebroski Henry A.3,Rai Urvashi2,Morrot Alexandre4,Zavala Fidel4,Steinman Ralph M.3,Nussenzweig Ruth S.2,Nussenzweig Michel C.15

Affiliation:

1. Laboratory of Molecular Immunology

2. Department of Medical and Molecular Parasitology, and Department of Pathology, New York University School of Medicine, New York, NY 10016

3. Laboratory of Cellular Physiology and Immunology,

4. Department of Molecular Microbiology and Immunology, Malaria Research Institute, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205

5. Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021

Abstract

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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