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Journal of Virology, December 2002, p. 11911-11919, Vol. 76, No. 23
0022-538X/02/$04.00+0 DOI: 10.1128/JVI.76.23.11911-11919.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Neonates Mount Robust and Protective Adult-Like CD8+-T-Cell Responses to DNA Vaccines
Jie Zhang, Nicole Silvestri, J. Lindsay Whitton, and Daniel E. Hassett*
The Scripps Research Institute, La Jolla, California 92037
Received 29 April 2002/
Accepted 27 August 2002
Neonates are thought to mount less vigorous adaptive immune responses than adults to antigens and infectious agents. This concept has led to a delay in the administration of many currently available vaccines until late infancy or early childhood. It has recently been shown that vaccines composed of plasmid DNA can induce both humoral and cell-mediated antimicrobial immunity when administered within hours of birth. In most of these studies, immune responses were measured weeks or months after the initial vaccination, and it is therefore questionable whether the observed responses were actually the result of priming of splenocytes within the neonatal period. Here we show that DNA vaccination at birth results in the rapid induction of antigen-specific CD8+ T cells within neonatal life. Analyses of T-cell effector functions critical for the resolution of many viral infections revealed that neonatal and adult CD8+ T cells produce similar arrays of cytokines. Furthermore, the avidities of neonatal and adult CD8+ T cells for peptide and the rapidity with which they upregulate cytokine production after recall encounters with antigen are similar. Protective immunity against the arenavirus lymphocytic choriomeningitis virus, which is mediated by CD8+ cytotoxic T cells, is also rapidly acquired within the neonatal period. Collectively these data imply that, at least in the case of CD8+ T cells, neonates are not as immunodeficient as previously supposed and that DNA vaccines may be an effective and safe means of providing critical cell-mediated antiviral immunity extremely early in life.
* Corresponding author. Mailing address: The Scripps Research Institute CVN-9, 10550 North Torrey Pines Rd., La Jolla, CA 92037. Phone: (858) 784-7497. Fax: (858) 784-7377. E-mail:
dhassett{at}scripps.edu.
This is manuscript no. 14962-NP from the Scripps Research Institute.
Journal of Virology, December 2002, p. 11911-11919, Vol. 76, No. 23
0022-538X/02/$04.00+0 DOI: 10.1128/JVI.76.23.11911-11919.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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