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DOI 10.1371/journal.pone.0167488

Медицинская библиотека · PloS one · 2017

Cell-Based Systems Biology Analysis of Human AS03-Adjuvanted H5N1 Avian Influenza Vaccine Responses: A Phase I Randomized Controlled Trial.

Howard Leigh M, Hoek Kristen L, Goll Johannes B, Samir Parimal, Galassie Allison, Allos Tara M, Niu Xinnan, Gordy Laura E, Creech C Buddy, Prasad Nripesh, Jensen Travis L, Hill Heather, Levy Shawn E, Joyce Sebastian, Link Andrew J, Edwards Kathryn M

Клиническое исследование I фазыСравнительное исследованиеСтатьяРандомизированное исследованиеПоддержка правительства СШАПоддержка NIH: внешняя программаПеревод пока не подготовлен

Аннотация

BACKGROUND

Vaccine development for influenza A/H5N1 is an important public health priority, but H5N1 vaccines are less immunogenic than seasonal influenza vaccines. Adjuvant System 03 (AS03) markedly enhances immune responses to H5N1 vaccine antigens, but the underlying molecular mechanisms are incompletely understood.

OBJECTIVE AND

METHODS

We compared the safety (primary endpoint), immunogenicity (secondary), gene expression (tertiary) and cytokine responses (exploratory) between AS03-adjuvanted and unadjuvanted inactivated split-virus H5N1 influenza vaccines. In a double-blinded clinical trial, we randomized twenty adults aged 18-49 to receive two doses of either AS03-adjuvanted (n = 10) or unadjuvanted (n = 10) H5N1 vaccine 28 days apart. We used a systems biology approach to characterize and correlate changes in serum cytokines, antibody titers, and gene expression levels in six immune cell types at 1, 3, 7, and 28 days after the first vaccination.

RESULTS

Both vaccines were well-tolerated. Nine of 10 subjects in the adjuvanted group and 0/10 in the unadjuvanted group exhibited seroprotection (hemagglutination inhibition antibody titer > 1:40) at day 56. Within 24 hours of AS03-adjuvanted vaccination, increased serum levels of IL-6 and IP-10 were noted. Interferon signaling and antigen processing and presentation-related gene responses were induced in dendritic cells, monocytes, and neutrophils. Upregulation of MHC class II antigen presentation-related genes was seen in neutrophils. Three days after AS03-adjuvanted vaccine, upregulation of genes involved in cell cycle and division was detected in NK cells and correlated with serum levels of IP-10. Early upregulation of interferon signaling-related genes was also found to predict seroprotection 56 days after first vaccination.

CONCLUSIONS

Using this cell-based systems approach, novel mechanisms of action for AS03-adjuvanted pandemic influenza vaccination were observed.

TRIAL REGISTRATION: ClinicalTrials.gov NCT01573312.

Для цитирования: Howard Leigh M, Hoek Kristen L, Goll Johannes B, Samir Parimal, Galassie Allison, Allos Tara M, Niu Xinnan, Gordy Laura E, Creech C Buddy, Prasad Nripesh, Jensen Travis L, Hill Heather, Levy Shawn E, Joyce Sebastian, Link Andrew J, Edwards Kathryn M. Cell-Based Systems Biology Analysis of Human AS03-Adjuvanted H5N1 Avian Influenza Vaccine Responses: A Phase I Randomized Controlled Trial.. PloS one. 2017. DOI: 10.1371/journal.pone.0167488.

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