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Impact of anti-orthopoxvirus neutralizing antibodies induced by a heterologous prime-boost HIV-1 vaccine on insert-specific immune responses
Authors:Stephen R Walsh  Michael S Seaman  Lauren E Grandpre  Cherie Charbonneau  Katherine E Yanosick  Barbara Metch  Michael C Keefer  Raphael Dolin  Lindsey R Baden
Institution:1. Division of Infectious Diseases, Brigham and Women''s Hospital, Boston, MA 02115, United States;2. Center for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Boston, MA 02115, United States;3. Harvard Medical School, Boston, MA 02115, United States;4. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, United States;5. Division of Infectious Diseases, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, United States
Abstract:

Background

The impact of anti-vector immunity on the elicitation of insert-specific immune responses is important to understand in vaccine development. HVTN 055 was a 150 person phase I randomized, controlled HIV vaccine trial of recombinant modified vaccinia Ankara (rMVA) and fowlpox (rFPV) with matched HIV-1 inserts which demonstrated increased CD8+ T-cell immune responses in the heterologous vaccine group. The controls used in this study were the empty vectors (MVA and FPV).

Methods

Anti-MVA and anti-vaccinia neutralizing antibodies (NAbs) were measured and compared with cellular and humoral HIV-1-specific immune responses.

Results

Elicitation of anti-vector responses increased with increasing dose of MVA and up to 2 administrations. Further inoculations of MVA (up to 5) did not increase the magnitude of the anti-MVA response but did delay the anti-vector NAb titre decay. There was no evidence that the insert impaired the anti-vector response, nor that anti-vector immunity attenuated the insert-specific responses.

Conclusion

Two doses of MVA may be ideal for the elicitation of orthopoxvirus immune responses with further doses maintaining increased titres against the vector. We found no evidence that eliciting HIV insert- or MVA vector-specific immune responses interfered with elicitation of immune responses to the other.
Keywords:Immunogenicity  Dose  MVA  Fowlpoxvirus  HIV vaccine  Prime-boost
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