Clinical trial in healthy malaria-naïve adults to evaluate the safety, tolerability, immunogenicity and efficacy of MuStDO5, a five-gene, sporozoite/hepatic stage Plasmodium falciparum DNA vaccine combined with escalating dose human GM-CSF DNA

نویسندگان

  • Thomas L. Richie
  • Yupin Charoenvit
  • Ruobing Wang
  • Judith E. Epstein
  • Richard C. Hedstrom
  • Sanjai Kumar
  • Thomas C. Luke
  • Daniel A. Freilich
  • Joao C. Aguiar
  • John B. Sacci, Jr.
  • Martha Sedegah
  • Ronald A. Nosek, Jr.
  • Patricia De La Vega
  • Mara P. Berzins
  • Victoria F. Majam
  • Esteban N. Abot
  • Harini Ganeshan
  • Nancy O. Richie
  • Jo Glenna Banania
  • Maria Fe B. Baraceros
  • Tanya G. Geter
  • Robin Mere
  • Lolita Bebris
  • Keith Limbach
  • Bradley W. Hickey
  • David E. Lanar
  • Jennifer Ng
  • Meng Shi
  • Peter M. Hobart
  • Jon A. Norman
  • Lorraine A. Soisson
  • Michael R. Hollingdale
  • William O. Rogers
  • Denise L. Doolan
  • Stephen L. Hoffman
چکیده

When introduced in the 1990s, immunization with DNA plasmids was considered potentially revolutionary for vaccine development, particularly for vaccines intended to induce protective CD8 T cell responses against multiple antigens. We conducted, in 1997-1998, the first clinical trial in healthy humans of a DNA vaccine, a single plasmid encoding Plasmodium falciparum circumsporozoite protein (PfCSP), as an initial step toward developing a multi-antigen malaria vaccine targeting the liver stages of the parasite. As the next step, we conducted in 2000-2001 a clinical trial of a five-plasmid mixture called MuStDO5 encoding pre-erythrocytic antigens PfCSP, PfSSP2/TRAP, PfEXP1, PfLSA1 and PfLSA3. Thirty-two, malaria-naïve, adult volunteers were enrolled sequentially into four cohorts receiving a mixture of 500 μg of each plasmid plus escalating doses (0, 20, 100 or 500 μg) of a sixth plasmid encoding human granulocyte macrophage-colony stimulating factor (hGM-CSF). Three doses of each formulation were administered intramuscularly by needle-less jet injection at 0, 4 and 8 weeks, and each cohort had controlled human malaria infection administered by five mosquito bites 18 d later. The vaccine was safe and well-tolerated, inducing moderate antigen-specific, MHC-restricted T cell interferon-γ responses but no antibodies. Although no volunteers were protected, T cell responses were boosted post malaria challenge. This trial demonstrated the MuStDO5 DNA and hGM-CSF plasmids to be safe and modestly immunogenic for T cell responses. It also laid the foundation for priming with DNA plasmids and boosting with recombinant viruses, an approach known for nearly 15 y to enhance the immunogenicity and protective efficacy of DNA vaccines.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2012