Skip to search boxSkip to navigationSkip to main content

Recombinant lentivector as a genetic immunization vehicle for antitumor immunity

*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Encouraged by remarkable successes in preventing infectious diseases and by the well-established potential of the immune system for controlling tumor growth, active therapeutic immunization approaches hold great promise for treating malignant tumors. In recent years, engineered recombinant viral vectors have been carefully examined as genetic-immunization vehicles and have been demonstrated to induce potent T-cell-mediated immune responses that can control tumor growth. Very recent efforts suggest that lentivectors possess important advantages over other candidate recombinant viral vectors for genetic immunization. Here, we review the development of recombinant lentivectors and the characteristics of T-cell immune responses elicited by lentivector immunization, including the mechanism of T-cell priming with a focus on the role of skin dendritic cells and potential applications for tumor immunotherapy.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 913-924 (12 pages)

Journal (Volume, Issue Number)

Expert Review of Vaccines (Volume 6, Issue 6)

Publication milestones

  • Published - 12/2007

Publication status

Published - 12/2007

ISSN

1476-0584

Publication IDs

  • Scopus: 37149001171
  • PubMed: 18377355

Publication metrics

Metrics

SciVal
citations
24
SciVal
FWCI
0.46
SciVal
Author count
3
SciVal
Paper percentile
77
Scopus
citations
Fractional count
2
Fractional count
0.67
Fractional count
1
Fractional count
0.33
Fractional count
2
Fractional count
1

PlumX, opens in new tab

Captures
16
Citation count
24

Funding Details

Researches conducted in the authors’ lab are supported by NIH grants and by start-up fund from MCG Cancer Center. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
FundersFunding number
MCG Cancer Center
-
NIH
-
NIAMS
K01AR047576