TY - JOUR
T1 - Aging exacerbates restraint stress-induced inhibition of antigen-specific antibody production in mice
AU - Ichihara, Yumiko
AU - Okano, Mitsuhiro
AU - Nishioka, Keiko
AU - Manabe, Noriko
AU - Ichihara, Naoto
AU - Jitsunari, Fumihiko
AU - Fujiwara, Tazuko
AU - Nizhizaki, Kazunori
N1 - Funding Information:
We wish to thank Yuko Okano for editorial assistance. This work was supported in part by grants for Research on Allergic Disease and Immunology by the Ministry of Health, Labour and Welfare (No. 14210301 to M.O.). This study was presented in part at the World Allergy Organization Congress XVIII ICACI, Vancouver, Canada, on September 10, 2003.
PY - 2009
Y1 - 2009
N2 - Background: We have recently found that exposure to acute restraint stress suppresses antigen-specific antibody production, including IgE, in a murine model of allergic rhinitis. Although age-related alterations in immune responses are known, it remains unclear whether aging modulates the antibody production under stressful conditions. In this study, we set out to determine the effects of aging on antibody production under acute restraint stress in mice. Methods: Both young and aged CBA/J mice were repeatedly sensitized intranasally with phospholipase A2 (PLA2) without adjuvants. Restraint stress was applied using uniform cylinders once a week for a continuous 8 h period, on 5 occasions in total. Blood samples were taken at 0, 20 and 30 days after primary sensitization, and production of PLA2-specific antibodies and levels of IL-4, IFN-γ, IL-10 and IL-1β in sera were determined by ELISA. Results: Repeated intranasal sensitization with PLA2 induced PLA2-specific IgE, IgG1 and IgG2a production in aged mice. We found that exposure to restraint stress significantly inhibited production of PLA2-specific IgE, IgG1 and IgG2a in aged mice. In addition, antibody production under restraint stress decreased significantly in aged mice when compared with young mice. No IL-4, IFN-γ, IL-10 or IL-1β were detected in sera from nonstressed or stressed aged mice. Conclusions: Aging exacerbates the immunosuppressive role of acute restraint stress in antigen-specific antibody production in mice.
AB - Background: We have recently found that exposure to acute restraint stress suppresses antigen-specific antibody production, including IgE, in a murine model of allergic rhinitis. Although age-related alterations in immune responses are known, it remains unclear whether aging modulates the antibody production under stressful conditions. In this study, we set out to determine the effects of aging on antibody production under acute restraint stress in mice. Methods: Both young and aged CBA/J mice were repeatedly sensitized intranasally with phospholipase A2 (PLA2) without adjuvants. Restraint stress was applied using uniform cylinders once a week for a continuous 8 h period, on 5 occasions in total. Blood samples were taken at 0, 20 and 30 days after primary sensitization, and production of PLA2-specific antibodies and levels of IL-4, IFN-γ, IL-10 and IL-1β in sera were determined by ELISA. Results: Repeated intranasal sensitization with PLA2 induced PLA2-specific IgE, IgG1 and IgG2a production in aged mice. We found that exposure to restraint stress significantly inhibited production of PLA2-specific IgE, IgG1 and IgG2a in aged mice. In addition, antibody production under restraint stress decreased significantly in aged mice when compared with young mice. No IL-4, IFN-γ, IL-10 or IL-1β were detected in sera from nonstressed or stressed aged mice. Conclusions: Aging exacerbates the immunosuppressive role of acute restraint stress in antigen-specific antibody production in mice.
KW - Aged mouse
KW - Immunosuppression
KW - Phospholipase A2
KW - Restraint stress
KW - Specific antibody
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U2 - 10.2332/allergolint.O-08-535
DO - 10.2332/allergolint.O-08-535
M3 - Article
C2 - 19153538
AN - SCOPUS:65449147833
SN - 1323-8930
VL - 58
SP - 119
EP - 124
JO - Allergology International
JF - Allergology International
IS - 1
ER -