The Flaviviridae family of RNA viruses includes numerous human disease-causing pathogens
that largely are increasing in prevalence due to continual climate change, rising
population sizes and improved ease of global travel. Escalating circulation of these
emerging and re-emerging pathogens draws attention to the need for vaccines to protect
against the severe diseases they cause, and this need is further exacerbated by their
transmission that occurs primarily through arthropod vectors. When constructing new,
efficacious vaccine candidates, several goals are targeted including safety, protective
capacity, ability to confer sustained protection, induction of neutralizing antibody
and protective T cell responses, as well as practicality.
Prophylactic vaccination as a means to protect against flavivirus infection has become
an intense area of research in the last several decades due to the inherent nature
of this family of viruses to cause explosive outbreaks [1]. However, even with the
enormous prevalence and impact on the human population, there are minimal flaviviruses
with approved human vaccines to date: yellow fever (YF), Japanese encephalitis virus
(JEV), tick-borne encephalitis virus (TBEV) and dengue virus (DENV) [2]. This Special
Issue highlights current studies that delve into research expanding the range of flavivirus
candidate vaccines. These findings are essential to advance the field and further
protect vulnerable populations from these disease-causing pathogens.
Although the members of the flavivirus family have been shown to be antigenically
similar [3], these viruses are indeed unique enough to often warrant varying vaccines.
This concept is highlighted by the four distinct DENV serotypes. DENV is widespread
and endemic in greater than 125 countries and currently accounts for an estimated
100–400,000,000 infections each year, with half of the world’s population being at
risk of infection [4]. As the four serotypes of DENV are distinct, infection with
one serotype results in only transient protection against the other three serotypes
[5], and each subsequent heterologous infection increases the risk for an infected
person to develop severe dengue.
Although there is a currently approved DENV vaccine, safety and efficacy data support
the need for alternative prophylactic vaccines to protect a broader population of
individuals. Strides toward this goal include virus-like particles (VLPs), which are
outlined in the review written by Wong et al. which summarizes VLP-based DENV vaccines
currently being tested. As noted by Wong et al., many of the current VLP-based DENV
vaccines lack the viral pre-Membrane (prM) protein; thus, it is believed these vaccines
will circumvent the induction of cross-reactive non-neutralizing antibodies that may
mediate antibody dependent enhancement. Importantly, these constructs still maintain
key structural components that induce T cell and antibody responses, like envelope
domain III (E DIII) against which most neutralizing antibodies are targeted [6]. Additionally,
such VLP vaccines have greater safety profiles than live-attenuated vaccines, which
have a higher risk of reverting to infectious virus in the elderly, a population that
has been shown to be at high risk for infection and difficult to vaccinate [7,8].
The case report presented by Domingo et al. features an instance where an elderly
individual received the YF vaccine prior to traveling to Brazil, then became ill and
experienced septic shock and multiorgan failure. It was soon determined that he already
had discernable YF antibodies a week after vaccination, in addition to high YF viral
load in serum, plasma, respiratory secretions and urine [9]. Thus, the benefits of
VLP vaccines include eliminating mutations to infectious virus in these critical,
vulnerable populations while maintaining antigenic structural proteins in a native
conformation.
Further, deeper understanding and advances in flavivirus genome structure and replication
cycles have been able to aid the development of other kinds of unique DENV vaccine
candidates. In this Issue, Park et al. outlines a candidate subunit vaccine based
on eliciting a strong neutralizing antibody response against E DIII. This vaccine
was developed to combat all four DENV serotypes by combining two subunits: partial
envelope domain II and consensus envelope domain III (cEDIII) [10]. The authors found
that an antibody purified from mice following immunization with this combined candidate
vaccine was strongly neutralizing compared to their single subunit vaccine containing
only cEDIII, with limited non-neutralizing antigen-specific antibody [10]. In addition,
this combined subunit vaccine was able to reduce DENV titers in several tissues when
compared to the single subunit vaccine, and conferred protection against DENV1, 2
and 4 in murine challenge models, thus showing promise as a candidate DENV subunit
vaccine [10]. Similarly, Tremblay et al. highlights how the discovery that flavivirus
vRNA 2′-O-methylation enables mimicry of cellular mRNAs has been instrumental in reverse
genetics studies to improve DENV vaccine design [11]. Specifically, when mutant DENV
clones are modified to encode a single point mutation in the viral nonstructural gene
5 (NS5) methyltransferase catalytic site, sensitivity to interferon treatment is enhanced,
and pre-treatment with such mutant viruses protects mice and monkeys from lethal DENV
infection [12]; this same approach has also proven successful in laboratory studies
seeking to formulate an alternative JEV vaccine construct [13].
In addition to the previously mentioned challenges of developing flavivirus vaccines,
another strong impediment to their development are practical considerations. As endemic
regions of flavivirus circulation tend to be rural, access to trained medical professionals
and refrigeration is often sparse. To counteract these obstacles, some vaccine constructs
are aimed at achieving formulations that are biologically stable over time and do
not require a medical professional to administer. In Muller et al., a tetravalent
E DENV subunit vaccine was administered via a microarray patch and, when compared
to traditional vaccination methods, led to enhanced neutralizing antibody titers to
all four DENV serotypes potentially due to the delivery of antigens in close proximity
to antigen presenting cells located beneath the skin. Inclusion of an adjuvant to
enhance immunogenicity led to complete protection in mice following DENV challenge
[14]. In addition to being efficacious, this form of vaccination would also be beneficial
to the population since a nanopatch can be administered by someone who is not medically
trained, and it does not require refrigeration.
This Special Issue also focuses its attention on Zika virus (ZIKV), a re-emerging
pathogen with a history of causing epidemics: 2007 (Yap islands), 2013 (French Polynesia)
and 2015 (South America) [15]. The 2015 ZIKV epidemic was rife with enhanced viral
spread due to travelers, further highlighting the need for a prophylactic vaccine
that can be administered to residents of ZIKV endemic areas, as well as to travelers.
Similar to DENV vaccination efforts, many trial ZIKV vaccines are formulated to elicit
strongly neutralizing antibodies, with several purified inactivated, live-attenuated
and DNA-based vaccines correlating with protection in mice, rhesus macaque animal
models and phase I human clinical trials [16,17,18]. In a study presented by Frumence
et al., a chimeric ZIKV vaccine clone was generated where the glycan loop of the viral
E protein of African strain MR766 was modified to encode three counterpart E glycan
loop amino acids of the epidemic strain, BeH819015, formulating a chimeric clone referred
to as ZIKVBeHMR-2. Following these substitutions and subsequent vaccination with ZIKVBeHMR-2,
neutralizing ZIKV antibodies were rapidly detected and effective at combatting MR766
challenge in mice [19].
In addition to the need for development and maintenance of strongly neutralizing antibodies
following vaccination, cellular responses have also proven to be essential in combatting
ZIKV, as it has been shown that CD4 and CD8+ T cells are critical in reducing viral
load and mortality in mouse models of ZIKV infection [20,21,22]. To this end, the
review written by Wong et al. highlights pre-Membrane:Envelope (prME) and Capsid:pre-Membrane:Envelope
(CprME) VLP-based vaccines that elicit T cell responses and stronger neutralizing
antibody responses than other DNA and formalin inactivated preparations [23,24]. As
previously mentioned, VLP-based vaccines have proven to be safer than live-attenuated
formulations, which will be key in ZIKV vaccine development since pregnant women are
classified as one of the most vulnerable populations. Nonetheless, in 2018, a live-attenuated
ZIKV vaccine that was protective in animal challenge models was tested in a phase
I clinical trial with support of the National Institutes of Health. The possibility
of reversion that comes with a live attenuated vaccine denotes the need for a metric
to examine mutation rates of such vaccines. In the study presented by Collins et al.,
next generation sequencing (NGS) was utilized to measure genetic diversity of live
attenuated candidate ZIKV vaccines and revealed that viral adaptation occurred throughout
cellular passages [25]. Thus, this study highlights a role for NGS in studying the
genetic stability of live attenuated vaccines.
Another article, co-authored by our group, also focused on ZIKV vaccine development,
highlighting another promising vaccine design avenue: adenovirus-vectors. These vectors
have increased in popularity over the last several years as vaccine platforms primarily
due to excellent safety profiles, the ability to be grown to high titers in cell culture,
capacity to induce strong inflammatory immune response, etc. [26]. Steffen et al.
developed an Early region 1A/Early region 3 (E1A/E3)-deleted adenovirus-vector ZIKV
vaccine that included an amino acid mutation to improve prM-E polypeptide processing,
in addition to including both B and T cell epitopes. Further highlighting the advantages
of vaccines that elicit both humoral and cell-mediated immune responses, we showed
that the vaccine construct was both immunogenic and efficacious in producing ZIKV-specific
CD4+, CD8+ and antibody responses that were protective in a murine ZIKV challenge
model [27]. Thus, this study provided strong evidence that an adenovirus-vector vaccine
against ZIKV has the ability to induce a potent immune response against this re-emerging
pathogen.
As this Special Issue highlights, developing vaccines for numerous members of the
Flaviviridae family has proven to be challenging for a variety of reasons, including
virus interplay with the immune system, a concept highlighted in the review written
by Tremblay et al. [11]. One vaccine approach which would alleviate the concerns of
flavivirus immune suppression on vaccine efficacy was highlighted by Wang et al. [28],
who sought to focus vaccine efforts on the vector rather than the pathogen. Since
many flaviviruses are often transmitted by the same species of arthropod vectors,
some research efforts have focused on generating vaccines against antigens produced
by the transmitting vector. Of particular note, it has been shown that an Aedes aegypti
salivary gland protein, AgBR1, shapes innate immune responses in murine models following
mosquito bites [29]. Based on this discovery, Wang et al. developed an AgBR1 adjuvanted
active immunization strategy in mice that led to the delay of lethal mosquito-transmitted
ZIKV infection [28]. This paper introduces an interesting concept where immunization
with a mosquito-derived protein could protect populations from numerous mosquito-spread
pathogens by targeting the innate immune response.
Hand in hand with vaccine design, methods of evaluation for vaccine efficacy are also
under intense research. In a study by Frumence et al., a flow cytometry-based neutralization
test (FNT) was employed as an alternative to the conventional plaque-reduction neutralization
test (PRNT) as a means to enable a high throughput screening strategy that does not
rely on methods requiring cell lines capable of fostering plaque formation. Through
the development of a GFP reporter of ZIKV, this study highlights the ability to measure
ZIKV neutralizing antibodies via flow cytometry with the antibody titers detected
being equivalent to those done by PRNTs in tandem [30]. Another promising way to evaluate
and enhance vaccine efficacy is highlighted in the study presented by Salat et al.
where mass spectrometry was used to analyze the content of two TBEV vaccines. Upon
confirming the presence of nonstructural protein 1 (NS1) in one vaccine tested, it
appeared to be highly immunogenic when administered to mice and was able to enhance
their survival following lethal virus challenge [31]. Thus, this study highlights
another viral protein, NS1, in addition to E that can enhance the protective capacity
of TBEV vaccines [31].
Overall, this Special Issue highlights numerous studies, reviews and a case report
that outline current research being done to further flavivirus vaccine development.
These studies address both the challenges of developing flavivirus vaccines and the
diverse and novel approaches to vaccine development that are currently underway. In
addition, this Special Issue also features work being done to improve pre-existing
vaccines, as well as techniques to streamline the process of determining vaccine efficacy
while confirming safety. While the rates of flavivirus infections continue to rise
globally, research efforts like the ones outlined in this Issue continually increase
our knowledge of flaviviruses, thus informing the development of novel vaccines which
will meet the growing need for protection against these pathogens.