Correlation of Cellular Immune Responses with Protection against Culture-Confirmed Influenza Virus in Young Children

American Society for Microbiology - Tập 15 Số 7 - Trang 1042-1053 - 2008
Bruce D. Forrest1,2, Michael W. Pride1,2, Andrew J. Dunning1,2, María Rosario Capeding3, Tawee Chotpitayasunondh4,3, John S. Tam5,6,7,8, Ruth Rappaport1,2, John H. Eldridge1,2, William C. Gruber6,7,2
1Research Institute for Tropical Medicine, Muntinlupa City, Philippines
2Wyeth Vaccines Research, 401 N. Middletown Road, Pearl River, New York 10960
3Queen Sirikit National Institute of Child Health, Bangkok 10400, Thailand
4; and Chinese University of Hong Kong, Hong Kong SAR, China
5Chinese University of Hong Kong, Hong Kong, SAR, China
6Sanofi Pasteur, Discovery Drive, Swiftwater, PA 18370.
7Wyeth Vaccines Re-search, 401 North Middletown Road, Pearl River, NY 10965.
8Wyeth Vaccines Research, 401 N. Middletown Road, Pearl River, NY 10960.

Tóm tắt

ABSTRACT

The highly sensitive gamma interferon (IFN-γ) enzyme-linked immunosorbent spot (ELISPOT) assay permits the investigation of the role of cell-mediated immunity (CMI) in the protection of young children against influenza. Preliminary studies of young children confirmed that the IFN-γ ELISPOT assay was a more sensitive measure of influenza memory immune responses than serum antibody and that among seronegative children aged 6 to <36 months, an intranasal dose of 107fluorescent focus units (FFU) of a live attenuated influenza virus vaccine (CAIV-T) elicited substantial CMI responses. A commercial inactivated influenza virus vaccine elicited CMI responses only in children with some previous exposure to related influenza viruses as determined by detectable antibody levels prevaccination. The role of CMI in actual protection against community-acquired, culture-confirmed clinical influenza by CAIV-T was investigated in a large randomized, double-blind, placebo-controlled dose-ranging efficacy trial with 2,172 children aged 6 to <36 months in the Philippines and Thailand. The estimated protection curve indicated that the majority of infants and young children with ≥100 spot-forming cells/106peripheral blood mononuclear cells were protected against clinical influenza, establishing a possible target level of CMI for future influenza vaccine development. The ELISPOT assay for IFN-γ is a sensitive and reproducible measure of CMI and memory immune responses and contributes to establishing requirements for the future development of vaccines against influenza, especially those used for children.

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