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Humoral and Cellular Immune Responses in Children Given Annual Immunization With Trivalent Inactivated Influenza Vaccine

Zeman, Alenka M. MD*; Holmes, Tyson H. PhD†; Stamatis, Shaye MS*; Tu, Wenwei MD, PhD*; He, Xiao-Song PhD§; Bouvier, Nancy PNP*; Kemble, George PhD‡; Greenberg, Harry B. MD§; Lewis, David B. MD*; Arvin, Ann M. MD*; Dekker, Cornelia L. MD*

Pediatric Infectious Disease Journal: February 2007 - Volume 26 - Issue 2 - pp 107-115
doi: 10.1097/01.inf.0000253251.03785.9b
Original Studies

Background: There have been no prior reports of the frequency of circulating influenza-specific, interferon gamma-producing memory CD4+ and CD8+ T-cells in healthy children who have received multiple influenza immunizations.

Methods: We evaluated 21 previously immunized children, ages 3 to 9 years, before and 1 month after administration of trivalent inactivated influenza vaccine. Frequencies of influenza-specific CD4+ and CD8+ T-cells stimulated with trivalent inactivated influenza vaccine or A/Panama (H3N2) virus were determined by flow cytometry, and antibody responses to vaccine strains and a drifted H3N2 strain were measured by hemagglutination inhibition assay and neutralizing antibody assays.

Results: Mean change in CD4+ and in CD8+ T-cell frequencies after immunization was 0.01% (P > 0.39) with postimmunization CD4+ frequencies higher than CD8+ frequencies. Children with more previous vaccinations had a higher baseline frequency of CD4+ T-cells (P = 0.0002) but a smaller increase or even a decline from baseline after immunization (P = 0.003). An association between age and change in frequency was not detected. Baseline geometric mean titers (GMTs) and seroprotection rates were significantly higher in older children against A/Panama (neutralizing baseline GMT, P = 0.0488) and A/New Caledonia (hemagglutination inhibition baseline GMT and seroprotection, P < 0.0297). Baseline GMTs against B/Hong Kong were not associated with age or quantity of prior vaccinations.

Conclusions: These findings suggest that children may plateau in CD4+ T-cell responses to influenza antigens with repeated exposures and that the number of exposures may play a large role in building a memory CD4+ T-cell response to influenza A, perhaps independently from age.

From the *Department of Pediatrics, the †Division of Biostatistics, Department of Health Research and Policy, and the §Department of Medicine and Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA; and ‡MedImmune Vaccines, Mountain View, CA.

Accepted for publication November 10, 2006.

Address for correspondence: Cornelia L. Dekker, MD, Division of Pediatric Infectious Diseases, Stanford University School of Medicine, 300 Pasteur Drive, Room G312, Stanford, CA 94305-5208. E-mail

© 2007 Lippincott Williams & Wilkins, Inc.