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. Author manuscript; available in PMC: 2010 Mar 3.
Published in final edited form as: Curr Top Microbiol Immunol. 2008;325:361–382. doi: 10.1007/978-3-540-77349-8_20

Table 1.

HCMV vaccines that have undergone evaluation in clinical trials.

CMV Vaccines Evaluated in Clinical Trials
Live, Attenuated Vaccines
AD169 Vaccine
  • Elicited HCMV-specific antibody responses in seronegative vaccine recipients

  • Significant injection-site and systemic reactogenicity

  • No ongoing studies active

Towne (+/rhIL12)
  • Elicits broad-based humoral and cellular immune responses

  • Favorable safety profile; no evidence for latency or viral shedding in recipients

  • Lack of efficacy for HCMV infection; reduced HCMV disease in renal transplant recipients

  • Augmentation of immunogenicity by inclusion of recombinant IL-12 in phase 1 studies

Towne/Toledo Chimera Vaccines
  • Favorable safety profile; no evidence for latency or viral shedding in recipients

  • Attenuated compared to Toledo strain of HCMV

  • No efficacy data available

Subunit Vaccines
Glycoprotein B/MF59 Adjuvant (CHO Cell Expression)
  • Favorable safety profile

  • High-titer neutralizing antibody and strong cell- mediated immune responses

  • Efficacy studies ongoing in young women, adolescents, renal transplant patients

Glycoprotein B/Canarypox Vector
  • Favorable safety profile

  • Suboptimal immunogenicity

  • “Prime-Boost” effect when administered in combination with Towne vaccine

pp65 (U83)/Canarypox Vector
  • Favorable safety profile

  • Strong antibody and cell-mediated immune responses

  • No efficacy data available

gB/pp65/IE1 Trivalent DNA Vaccine
gB/pp65 Bivalent DNA Vaccine
  • DNA vaccine adjuvanted with poloxamer adjuvant and benzalkonium chloride

  • Phase I studies completed

  • Phase 2 study ongoing with bivalent gB/pp65 vaccine in HSC transplant recipients

gB/pp65/IE1 Alphavirus Replicon Trivalent Vaccine
  • Engineered using replication-deficient alphavirus technology

  • Generation of virus-like replicon particles (VRPs)

  • Phase 1 clinical trial recently initiated