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Updated: Jul 15, 2025

Skin Tattooing As A Novel Approach For DNA Vaccine Delivery
Published on: October 18, 2012
Immune responses, therapeutic anti-tumor effects, and tolerability upon therapeutic HPV16/18 E6/E7 DNA vaccination
Shiwen Peng1, Hsin-Fang Tu1, Michelle Cheng1
1Department of Pathology, Johns Hopkins University , Baltimore, Maryland, USA.
Importance:
Respectively, HPV16 and HPV18 cause 50% and 20% of cervical cancer cases globally. Viral proteins E6 and E7 are obligate drivers of oncogenic transformation. We recently developed a candidate therapeutic DNA vaccine, pBI-11, that targets HPV16 and HPV18 E6 and E7. Single-site intramuscular delivery of pBI-11 via a needle elicited therapeutic anti-tumor effects in mice and is now being tested in high-risk human papillomavirus+ head and neck cancer patients (NCT05799144). Needle-free biojectors such as the Tropis device show promise due to ease of administration, high patient acceptability, and the possibility of improved delivery. For example, vaccination of patients with the ZyCoV-D DNA vaccine using the Tropis device is effective against COVID19, well tolerated, and licensed. Here we show that split-dose, multi-site administration and intradermal delivery via the Tropis biojector increase the delivery of pBI-11 DNA vaccine, enhance HPV antigen-specific CD8+ T-cell responses, and improve anti-tumor therapeutic effects, suggesting its translational potential to treat HPV16/18 infection and disease.
Insights
Needle-free delivery of a novel DNA vaccine targeting human papillomavirus (HPV) E6 and E7 proteins enhanced anti-tumor effects. This approach shows promise for treating HPV-related cancers.
Area of Science:
- Oncology
- Immunology
- Vaccinology
Background:
- Human papillomavirus (HPV) types 16 and 18 are major causes of cervical cancer.
- The viral oncoproteins E6 and E7 are critical for oncogenic transformation.
- A DNA vaccine candidate, pBI-11, targeting HPV16/18 E6 and E7, demonstrated therapeutic anti-tumor effects via intramuscular injection.
Purpose of the Study:
- To evaluate the efficacy of needle-free intradermal delivery of the pBI-11 DNA vaccine using the Tropis biojector.
- To assess the impact of split-dose, multi-site administration on vaccine delivery and immune response.
- To determine the translational potential of this enhanced delivery method for HPV-related diseases.
Main Methods:
- Split-dose, multi-site intradermal administration of the pBI-11 DNA vaccine via the Tropis biojector in a preclinical model.
- Assessment of vaccine DNA delivery efficiency.
- Quantification of HPV antigen-specific CD8+ T-cell responses.
- Evaluation of anti-tumor therapeutic effects.
Main Results:
- Intradermal delivery via the Tropis biojector increased pBI-11 DNA vaccine delivery compared to needle injection.
- Split-dose, multi-site administration enhanced HPV antigen-specific CD8+ T-cell responses.
- Improved anti-tumor therapeutic effects were observed with the Tropis biojector delivery method.
Conclusions:
- Needle-free, intradermal delivery of the pBI-11 DNA vaccine using the Tropis biojector enhances immune responses and anti-tumor efficacy.
- This delivery strategy holds translational potential for treating HPV16/18 infections and associated cancers.
- The Tropis biojector offers a patient-friendly alternative for DNA vaccine administration.
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