Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT03663998 |
| Other study ID # |
14SM2306 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
Phase 1
|
| First received |
|
| Last updated |
|
| Start date |
August 15, 2015 |
| Est. completion date |
April 10, 2018 |
Study information
| Verified date |
January 2021 |
| Source |
Imperial College London |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
This is a two part study to evaluate the immunogenicity and tolerability of DNA-C CN54ENV
plasmid DNA (CN54ENV) administered with electroporation (EP), with and without DNA encoding
recombinant interleukin-12 (GENEVAX® IL-12). Part 1 is exploratory and designed to select
conditions capable of promoting enhanced B cell responses in a limited number of volunteers.
Part 2 is dependent upon Part 1 and is designed to study the fine specificity of the B-cell
immune responses to CN54ENV DNA in an expanded number of subjects. Data from both stages will
be combined for safety and immunological analysis.
Description:
It is generally accepted that globally effective HIV-1 vaccine will likely need to induce
bnAbs against HIV-1. The proposed study is based on the recognition of the potential
strategic importance of performing iterative small human studies to accelerate HIV-1
immunogen discovery, where DNA vaccines offer the fastest and most cost effective approach
for rapid screening of multiple immunogens. This study aims to leverage DNA immunization as a
platform to accelerate the discovery of HIV-1 immunogens capable of inducing bnAbs in humans.
To meet this aim this study seeks to apply recent state of the art technological advances in
DNA vaccination and immune monitoring, both at the single cell and molecular level, to enable
detailed probing of developing vaccine induced antibody responses. In this respect it
represents the first attempt in humans to use a DNA vaccine approach to investigate the
development and focusing of B cell responses to vaccination. Should this approach be
successful it will provide an important new strategy for rapidly conducting systematic
clinical research studies in humans aimed at moving the HIV-1 vaccine field closer to
achieving the key objective of identification of immunogens and vaccine strategies required
for induction of bnAbs in humans.
At the end of 2012, an estimated 35.3 million people were living with HIV worldwide, up 17%
from 2001. This reflects the continued large number of new HIV infections and a significant
expansion of access to antiretroviral therapy, which has helped reduce AIDS-related deaths,
especially in more recent years (UNAIDS Report on the global AIDS epidemic 2013. Geneva
2013). The majority of new HIV infections continue to occur in sub-Saharan Africa. There is
an urgent need to strengthen and scale-up existing and new prevention methods such as HIV
testing and counselling, behavioural interventions, condom use, treatment of sexually
transmitted diseases, harm reduction, male circumcision (Wamai, Morris et al. 2011) and
antiretroviral drugs for prevention (Granich, Gupta et al. 2011). New prevention strategies
to control the epidemic and prevent new infections, including pre-exposure prophylaxis (Kim,
Becker et al. 2010), antiviral treatment for prevention (Granich, Lo et al. 2011), topical
microbicides (Krakower and Mayer 2011), and HIV preventive vaccines must be explored and
their access ensured. However the development of an efficacious preventive vaccine against
HIV-1 remains among the best hopes for controlling the HIV/AIDS pandemic (Kim, Rerks-Ngarm et
al. 2010, Koff 2010).
Data from a recent community-based efficacy trial in Thailand (RV144) testing a vaccination
regimen consisting of priming with the canarypox vector ALVAC-HIV, expressing HIV gag, pro,
and env genes, and boosting with recombinant AIDSVAX B/E HIV Env protein demonstrated modest
vaccine protection against HIV acquisition. The vaccine efficacy decreased over the first
year after vaccination from 60% at one year to 31.2 % at 3.5 years post first vaccination,
suggesting that protection may be related to HIV-specific antibodies waning over time
(Rerks-Ngarm, Pitisuttithum et al. 2009). The regimen did not decrease HIV viral load in
vaccine recipients who acquired HIV. CD8 T-cell responses were in few vaccine recipients,
while binding antibodies were detected in a majority of them, with very limited detectable
neutralizing antibody responses to HIV. These results suggest that more potent vaccines are
needed for providing significant and sustained protection against HIV acquisition as well as
for controlling viral replication.
Neutralizing antibodies against circulating isolates are induced principally by HIV Env and
could potentially confer sterilizing immunity against HIV, as suggested by non-human primate
SHIV challenge studies (Mascola, Stiegler et al. 2000, Pantophlet and Burton 2006, Hessell,
Poignard et al. 2009). Moreover, a recent Non Human Primates (NHP) study demonstrates that
SIV (Simian Immunodeficiency Virus) Env antigen was essential to confer protection against
SIV challenge and that SIV Env-specific binding non-neutralizing antibodies played a role in
this protection (Barouch, Liu et al. 2012). Previous trials using monomeric AIDSVAX gp120
showed no efficacy in a phase III trials (Flynn, Forthal et al. 2005, Pitisuttithum, Gilbert
et al. 2006). This failure has been a major drawback for Env-based HIV vaccines, since
current immunogens afford only very narrow protection against HIV strains that are closely
related to the vaccine antigen (Zhang and Dimitrov 2007, Montero, van Houten et al. 2008). In
RV144, an analysis of the correlates of risk showed that IgG3 binding antibodies to
scaffolded-V1V2 recombinant protein correlated inversely with infection rate while Env
binding plasma IgA correlated directly with infection rate (Haynes, Gilbert et al. 2012).
Several lines of evidence suggest that vaccine induced antibodies recognize conformational
epitopes in the scaffolded V1V2 reagent, which has been shown to detect conformational V1V2
antibodies (Pinter, Honnen et al. 1998, Zolla-Pazner, deCamp et al. 2013). The results of an
analysis of breakthrough viruses from patients in the RV144 trial were consistent with immune
pressure focused on amino acid patterns in and flanking the V1V2 region of HIV-1 Env
(Edlefsen, Gilbert et al. 2013). This region serves critical functions, such as participating
in CD4-receptor and chemokine-receptor binding, binding to α4β7 integrin (Nawaz, Cicala et
al. 2011) and serving as the binding site of neutralizing antibodies (Gorny, Stamatatos et
al. 2005, Walker, Phogat et al. 2009, Changela, Wu et al. 2011, McLellan, Pancera et al.
2011). However, the search for an immunogen able to induce broad cross-protective and
long-lasting neutralizing/functional antibodies remains difficult and critical (Burton,
Desrosiers et al. 2004, Montefiori, Sattentau et al. 2007).
During the vast majority of natural HIV infections, the antibody response which develops is
"too little, too late" - occurring approximately 12 weeks from initial exposure which is
after viral expansion has occurred (McMichael, Borrow et al. 2010). Recent data also suggests
that under normal circumstances, heterosexual transmission is a relatively rare event and
that there is a small "window of opportunity" - in the order of days - during which it might
be possible to stop the establishment of a latent infection. An ideal vaccine would prime a
very early and broad antibody response targeting multiple neutralizing epitopes for effective
control of early viral replication. However, bnAbs typically only arise in only 1% of
chronically infected subjects, take several years to develop, display exceptional levels of
somatic hyper mutation, have unusually long CDR3 regions and exhibit significant
glycan-binding, properties not induced by current vaccine candidates. Thus elicitation of
broadly neutralizing antibodies (bnAbs) against HIV-1 is both a problem of Immunogen Design
and Human Immune Responsiveness.
Despite significant progress in identifying broadly neutralizing antibodies in a very small
number of infected individuals, and detailed characterization of their cognate epitopes,
attempts to design appropriate immunogens inducing HIV-specific broadly neutralizing
antibodies have so far failed. Indeed, next generation vaccines are likely to be critically
dependent upon discovery of novel immunogens capable of eliciting protective responses in
humans. However, this is limited by the current lack of understanding as to how immunogens
induce protective antibody responses, their gene usage, their maturation pathways, and
factors facilitating breadth and potency. While animal studies have played an important role
in understanding the pathogenesis of HIV and related retroviruses, they are quite limited
when it comes to modelling human immunization studies due to differences in immunogenetics
and species specificity. The advent of technological advances that probe human immune
responsiveness at the single cell and molecular level now provide the necessary tools to look
beyond pre-clinical models to resolve these issues. Indeed, a strong argument for increased
and improved early clinical studies in humans (instead of the currently lengthy process of
prior extensive animal testing) is that animals, including non-human primates (NHP), may not
accurately recapitulate germline engagement of B cells, which could be critical for vaccines
designed to induce HIV-1 envelope (Env) bnAbs. To resolve this, it is now generally agreed
that rapid, iterative, small, experimental early human vaccine studies are needed to select
and refine the best approaches to immunogen design. Such an approach would allow rapid
selection of the most promising vaccine strategies at an early stage thereby reducing the
risk of failure in more advanced phase clinical development. However, the cost and lengthy
time lines associated with the manufacture of recombinant proteins means it is not feasible
to test multiple iterations of HIV-1 envelope structures. In contrast, DNA vaccines offer a
rapid and feasible approach for screening multiple immunogens in human trials based on ease
of manufacture and reduced costs.
Although early approaches to DNA vaccination failed to induce significant antibody responses
in humans, more recent trials have shown that DNA vaccines can induce neutralizing antibodies
against a number of viruses (Martin, Pierson et al. 2007, Martin, Louder et al. 2008,
Ledgerwood, Pierson et al. 2011, Ledgerwood, Hu et al. 2012) and detectable antibody
responses to HIV-1 (Catanzaro, Roederer et al. 2007). Various strategies can now be used to
improve and augment the immunogenicity of DNA vaccines including: promoter selection and
codon optimization; the use of electroporation (EP); the route of administration
(intramuscular (IM) or intradermal (ID)); and the use of molecular adjuvants such as IL-12
(Sardesai and Weiner 2011, Yin, Dai et al. 2011, Kopycinski, Cheeseman et al. 2012). The
additional advantage provided by lack of anti-vector immunity associated with other delivery
platforms (viral vectors) provides the opportunity for serial immunizations with multiple DNA
derived immunogens. In this context DNA vaccination offers the potential to provide targeted
germline priming that may critically redirect antibody responses upon protein boosting
(Schittek and Rajewsky 1990, Yoshida, Mei et al. 2010). Furthermore, the lack of vector
immunity would allow the use of a series of DNA encoded immunogens to engage germline B cells
and direct them towards recognition of bnAb epitopes prior to amplification by protein
boosting. While multiple dose DNA vaccination may not represent a practical approach to a
prophylactic mass vaccination campaign, its potential to induce antibody responsiveness may
make it an important clinical research tool for immunogen discovery and refinement in humans.
The real power of such an approach can only now be fully realized through the development of
advanced tools for monitoring immune response evolution at the single cell and molecular
level. Here the ability to clone Ab genes from individual responding human B cells provides
the opportunity to glean new insights into the specificity and functionality of evolving Ab
repertoires, while next generation sequencing (NGS) approaches facilitate evolutionary study
of responses at the clonotypic level. This project seeks to apply these tools to proof of
concept (POC) studies aimed at demonstrating that DNA vaccination can provide a valuable tool
to systematically probe evolving Ab repertoires in humans.
