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*Flu
The Journal of Immunology, 2006, 176: 6333-6339.
Copyright © 2006 by The American Association of Immunologists

T Cell Responses Are Better Correlates of Vaccine Protection in the Elderly1

Janet E. McElhaney2,*, Dongxu Xie*, W. David Hager{dagger}, Mary Beth Barry{dagger}, Yazhen Wang§, Alison Kleppinger{ddagger}, Catherine Ewen, Kevin P. Kane and R. Chris Bleackley||

* Center for Immunotherapy of Cancer and Infectious Diseases, {dagger} Division of Cardiology, and {ddagger} UConn Center on Aging, Department of Medicine, University of Connecticut School of Medicine, Farmington, CT 06030; § Department of Statistics, University of Connecticut, Storrs, CT 06269; and Department of Medical Microbiology and Immunology and || Department of Biochemistry, University of Alberta, Edmonton, Alberta, Canada

It is commonly held that increased risk of influenza in the elderly is due to a decline in the Ab response to influenza vaccination. This study prospectively evaluated the relationship between the development of influenza illness, and serum Ab titers and ex vivo cellular immune responses to influenza vaccination in community dwelling older adults including those with congestive heart failure (CHF). Adults age 60 years and older (90 subjects), and 10 healthy young adult controls received the 2003-04 trivalent inactivated influenza vaccine. Laboratory diagnosed influenza (LDI) was documented in 9 of 90 older adults. Pre- and postvaccination Ab titers did not distinguish between subjects who would subsequently develop influenza illness (LDI subjects) and those who would not (non-LDI subjects). In contrast, PBMC restimulated ex vivo with live influenza virus preparations showed statistically significant differences between LDI and non-LDI subjects. The mean IFN-{gamma}:IL-10 ratio in influenza A/H3N2-stimulated PBMC was 10-fold lower in LDI vs non-LDI subjects. Pre-and postvaccination granzyme B levels were significantly lower in CHF subjects with LDI compared with subjects without LDI. In non-CHF subjects with LDI, granzyme B levels increased to high levels at the time of influenza infection. In conclusion, measures of the ex vivo cellular immune response to influenza are correlated with protection against influenza while serum Ab responses may be limited as a sole measure of vaccine efficacy in older people. Ex vivo measures of the cell-mediated immune response should be incorporated into evaluation of new vaccines for older adults.




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