TY - JOUR
T1 - Human Effector and Memory CD8+ T Cell Responses to Smallpox and Yellow Fever Vaccines
AU - Miller, Joseph D.
AU - van der Most, Robbert G.
AU - Akondy, Rama S.
AU - Glidewell, John T.
AU - Albott, Sophia
AU - Masopust, David
AU - Murali-Krishna, Kaja
AU - Mahar, Patryce L.
AU - Edupuganti, Srilatha
AU - Lalor, Susan
AU - Germon, Stephanie
AU - Del Rio, Carlos
AU - Mulligan, Mark J J.
AU - Staprans, Silvija I.
AU - Altman, John D.
AU - Feinberg, Mark B.
AU - Ahmed, Rafi
PY - 2008/5/16
Y1 - 2008/5/16
N2 - To explore the human T cell response to acute viral infection, we performed a longitudinal analysis of CD8+ T cells responding to the live yellow fever virus and smallpox vaccines-two highly successful human vaccines. Our results show that both vaccines generated a brisk primary effector CD8+ T cell response of substantial magnitude that could be readily quantitated with a simple set of four phenotypic markers. Secondly, the vaccine-induced T cell response was highly specific with minimal bystander effects. Thirdly, virus-specific CD8+ T cells passed through an obligate effector phase, contracted more than 90% and gradually differentiated into long-lived memory cells. Finally, these memory cells were highly functional and underwent a memory differentiation program distinct from that described for human CD8+ T cells specific for persistent viruses. These results provide a benchmark for CD8+ T cell responses induced by two of the most effective vaccines ever developed.
AB - To explore the human T cell response to acute viral infection, we performed a longitudinal analysis of CD8+ T cells responding to the live yellow fever virus and smallpox vaccines-two highly successful human vaccines. Our results show that both vaccines generated a brisk primary effector CD8+ T cell response of substantial magnitude that could be readily quantitated with a simple set of four phenotypic markers. Secondly, the vaccine-induced T cell response was highly specific with minimal bystander effects. Thirdly, virus-specific CD8+ T cells passed through an obligate effector phase, contracted more than 90% and gradually differentiated into long-lived memory cells. Finally, these memory cells were highly functional and underwent a memory differentiation program distinct from that described for human CD8+ T cells specific for persistent viruses. These results provide a benchmark for CD8+ T cell responses induced by two of the most effective vaccines ever developed.
KW - CELLIMMUNO
UR - http://www.scopus.com/inward/record.url?scp=43049154506&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=43049154506&partnerID=8YFLogxK
U2 - 10.1016/j.immuni.2008.02.020
DO - 10.1016/j.immuni.2008.02.020
M3 - Article
C2 - 18468462
AN - SCOPUS:43049154506
SN - 1074-7613
VL - 28
SP - 710
EP - 722
JO - Immunity
JF - Immunity
IS - 5
ER -