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Zika Virus
Zika Virus
Zika Virus
incredibly time-sensitive issue, since people are pregnant now and will be
tomorrow.
Vaccines may be a promising solution to the problem. Although it is difficult
to engineer vaccines for every pathogen, many laboratories are coming close
to having a prototype of a vaccine they hope will be the answer. Phase 1
trials are set to start at the beginning this summer. However, Phase 1 trials
are just the beginning as there are phase 2 and phase 3 trials to be done,
and the very earliest that a vaccine could be widely distributed is 2018,
according to reports by BBC.
In addition, there are some concerns that must be kept in mind when
developing such a vaccine. Since this Zika virus has been linked not only to
microcephaly, but also to Guillan-barre syndrome, it changes how we must
approach the problem. Guillan-barre is an autoimmune condition. Most often,
it occurs after infection by bacteria Campylobacter jejuni. It is not the actual
bacteria that causes the syndrome, but rather, the activated immune system
that overreacts and mounts an extreme host response. In doing so, the
immune system attacks structures that may momecularly mimic the
pathogen. The immune system attacks peripheral myelin and destroys
Schwann cells, causing inflammation and demyelination of peripheral nerves
and motor fibers. This results in the clinic symptoms of symmetric ascending
muscle weakness/paralysis beginning in the lower extremities. Facial
paralysis is see in 50% of cases, and autonomic dysregulation or sensory
abnormalities (such as cardiac irregularities, hypertension, hypotension) may
also occur. Paralysis can affect the diaphragm, causing respiratory failure.
While the mortality rate is rather low, this is obviously a debilitating disease
that one should be wary of.
This leads us to question the use of vaccines in preventing Zika virus
transmission. Since vaccines contain either killed or attenuated components
of the virus to stimulate the hosts immune system to recognizing the
antigen in the future, there is a chance that the act of introducing these
molecules and activating the immune response may lead to Guillan-barre. It
is still unclear what exactly causes the molecular mimicry and overactivation
of the immune system seen in Guillan-barre. Thus, it is not impossible that
even killed viral particles could start an immune response leading to Guillanbarre.
We thus need some more data. If we are to compare the risk of microcephaly
to the risk of Guillan-barre, and whether we as a community are willing to
take either risk over the other, we must have hard data to make an informed
decision. Since this is a time-sensitive issue, it is imperative that research be
done now, and that we remain aware of the downfalls of each potential
option.