Long-term efficacy and immune responses following immunization with the RTS,S malaria vaccine

被引:205
作者
Stoute, JA
Kester, KE
Krzych, U
Wellde, BT
Hall, T
White, K
Glenn, G
Ockenhouse, CF
Garcon, N
Schwenk, R
Lanar, DE
Sun, P
Momin, P
Wirtz, RA
Golenda, C
Saloui, M
Wortmann, G
Holland, C
Dowler, M
Cohen, J
Ballou, WR
机构
[1] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Dept Immunol, Div Communicable Dis & Immunol, Washington, DC 20307 USA
[2] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Dept Entomol, Div Communicable Dis & Immunol, Washington, DC 20307 USA
[3] Walter Reed Army Med Ctr, Walter Reed Army Inst Res, Dept Membrane Biochem, Div Communicable Dis & Immunol, Washington, DC 20307 USA
[4] SmithKline Beecham Biol, Rixensart, Belgium
关键词
D O I
10.1086/515657
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The malaria sporozoite vaccine candidate RTS,S, formulated with an oil-in-water emulsion plus the immunostimulants monophosphoryl lipid A and the saponin derivative QS21 (vaccine 3), recently showed superior efficacy over two other experimental formulations, Immunized volunteers were followed to determine the duration of protective immune responses, Antibody levels decreased to between one-third and one-half of peak values 6 months after the last dose of vaccine. T cell proliferation and interferon-gamma production in vitro were observed in response to RTS,S or hepatitis B surface antigen, Seven previously protected volunteers received sporozoite challenge, and 2 remained protected (1/1 for vaccine 1, 0/1 for vaccine 2, and 1/5 for vaccine 3). The prepatent period was 10.8 days for the control group and 13.2 days for the vaccinees (P < .01). Immune responses did not correlate with protection. Further optimization in vaccine composition and/or immunization schedule will be required to induce longer-lasting protective immunity.
引用
收藏
页码:1139 / 1144
页数:6
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