Abstract | BACKGROUND: A pediatric vaccine to prevent breast milk transmission of human immunodeficiency virus (HIV) may generate greater immune responses at viral entry sites if given by an oral route. METHODS: We compared immune responses induced in juvenile macaques by prime/boosting with simian immunodeficiency virus (SIV)-expressing DNA/modified vaccinia Ankara virus (MVA) by the intramuscular route (IM), the oral (O)/tonsillar routes (T), the O/sublingual (SL) routes, and O+IM/SL routes. RESULTS: O/T or O/SL immunization generated SIV-specific T cells in mucosal tissues but failed to induce SIV-specific IgA in saliva or stool or IgG in plasma. IM/IM or O+IM/SL generated humoral and cellular responses to SIV. IM/IM generated greater frequencies of TFH in spleen, but O+IM/SL animals had higher avidity plasma IgG and more often demonstrated mucosal IgA responses. CONCLUSION: These results suggest that codelivery of HIV DNA/MVA vaccines by the oral and IM routes might be optimal for generating both systemic and mucosal antibodies.
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Authors | Alan D Curtis 2nd, Kara Jensen, Koen K A Van Rompay, Rama R Amara, Pamela A Kozlowski, Kristina De Paris |
Journal | Journal of medical primatology
(J Med Primatol)
Vol. 47
Issue 5
Pg. 288-297
(10 2018)
ISSN: 1600-0684 [Electronic] Denmark |
PMID | 30204253
(Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural)
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Copyright | © 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- DNA, Viral
- SAIDS Vaccines
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Topics |
- Administration, Oral
- Administration, Sublingual
- Animals
- DNA, Viral
(adverse effects)
- Immunity, Cellular
(immunology)
- Immunity, Mucosal
(immunology)
- Immunogenicity, Vaccine
(immunology)
- Injections, Intramuscular
(adverse effects)
- Macaca mulatta
- Monkey Diseases
(immunology)
- Proof of Concept Study
- SAIDS Vaccines
(adverse effects)
- Simian Immunodeficiency Virus
(immunology)
- Vaccinia
(immunology)
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