COVID-19 vaccine development

NIH Pandemic-Era Grants

Pandemic Era Grants

2022

Document text

Principal Investigator: George N. Pavlakis
Organization: DIVISION OF BASIC SCIENCES - NCI
Fiscal Year: 2022
Award: $505,395
Funding agency: National Cancer Institute

A collection of human samples is being analyzed to examine in detail humoral and      cellular immunity after natural infection. These patients recovered from infection and      accepted to donate convalescent plasma for transfer to hospitalized patients in an approved      clinical trial. The immune response of these cohort is studied longitudinally to identify the      nature and longevity of immune response. In addition, the recipient patients will be studied      in an effort to identify benefits of immunotherapy after plasma transfer. The results of      analysis of natural infection will be important in the design of vaccine strategies. The      identification of patients with high titers of neutralizing antibodies will also support the      selection of plasma collection for transfer to hospitalized patients as immunotherapy. We      studied SARS-CoV-2 antibody maintenance in this cohort of infected convalescent people in      Athens, Greece. SARS-CoV-2 antibody kinetics eight months from COVID-19 onset: Persistence of      spike antibodies but loss of neutralizing antibodies in 24% of convalescent plasma donors was      observed. We continue to follow this cohort for 14 months and we determine Antibody longevity      and neutralizing activity. In collaboration with Dr. Felber's Section we have developed DNA      vectors that induced strong immune response in macaques after two vaccinations. Our strategy      is to induce both neutralizing Ab and also cellular immunity able to optimally suppress virus      infection. Several forms of SARS-CoV-2 antigens were expressed in DNA vectors and were tested      in animals after characterization. Macaque vaccination showed that the animals develop robust      immune responses. We showed that these responses to be protective after virus challenge, thus      giving the opportunity to develop prophylactic vaccines against SARS-CoV-2 based on DNA      technology that also provides much higher cellular immune responses. These responses may lead      to vaccines with superior longevity and effectiveness compared with the current generation. We      characterized the cytokine and chemokine responses to the 1st and 2nd dose of the BNT162b2      mRNA (Pfizer/BioNtech) vaccine in antigen-naive and in previously coronavirus disease 2019      (COVID-19)-infected individuals (NCT04743388). Transient increases in interleukin-15 (IL-15)      and interferon gamma (IFN-gamma) levels early after boost correlated with Spike antibody      levels, supporting their use as biomarkers of effective humoral immunity development in      response to vaccination. We identified a systemic signature including increases in IL-15,      IFN-gamma, and IP-10/CXCL10 after the 1st vaccination, which were enriched by tumor necrosis      factor alpha (TNF-alpha) and IL-6 after the 2nd vaccination. In previously COVID-19-infected      individuals, a single vaccination resulted in both strong cytokine induction and antibody      titers similar to the ones observed upon booster vaccination in antigen-naive individuals, a      result with potential implication for future public health recommendations. We expanded our      studies to immunocompromised individuals including patients with hematological malignancies, a      population at high risk of developing severe disease upon SARS-CoV-2 infection. Protection      afforded by vaccination is frequently low and the biology leading to altered vaccine efficacy      is not fully understood. Overall, the patients showed heterogeneous adaptive and innate      responses with lower humoral (binding and neutralizing antibodies) and reduced innate cytokine      responses (IFN-gamma, IL-15 and IP-10/CXCL10 signature) to vaccination compared to naive      vaccine recipients. Changes in IFN-g and IP-10/CXCL10 at priming vaccination and IFN-g, IL-15,      IL-7 and IL-10 upon booster vaccination correlated with the Spike antibody magnitude and were      predictive of successful antibody development. The pattern of responses described offer novel      prognostic approaches for potentiating the effectiveness of COVID-19 vaccination in transplant      patients with hematological malignancies. We are expanding our research of the development of      adaptive and innate immune responses upon COVID-19 vaccination to other cancer      cohorts.

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