The topic of
my entry this week will combine the subject matter of two previous posts:
septic infections and viruses.
It may sound strange, but some study has been
done that suggests that it may be possible to monitor progression/severity of
septic infections through the detection of previously latent viruses,
indicating a clinically significant depressed immune system. In order to accomplish this, several serially
collected blood and/or plasma samples were obtained from hospitalized patients
over a period of time and monitored for an increase in viral DNA from species
that are capable of becoming latent, or hiding within the host’s DNA. Examples of these which were used in the
study included cytomegalovirus (CMV), Epstein-Barr (EBV), and herpes-simplex
(HSV).1
In theory,
when the immune system is suppressed to a certain extent, these latent viruses
would be reactivated and enter the patient’s blood. For the purpose of this study, an increase in
the viral DNA present in the patient’s blood was cross correlated to secondary
infections such as bacteria and fungi to see if a relationship could be
established, which could be used to indicate the underlying status of the
corresponding person’s immune system.1
It was
determined that this method of serially monitoring the amount of virus present
in a septic patient’s blood could be useful in determining the severity of the
depression of the immune system. The authors
suggest that this could be best accomplished through monitoring a panel of
common viruses such as CMV, EBV, HSV as well as others, and observed for a
marked increase across the board which could indicate that an individual has
entered the immunosuppressive stage of sepsis meaning that they would be almost
incapable of fighting off infections from various opportunistic pathogens such
as bacteria and fungi.1
If you would
like to read the full article and see the figures, here is the link:
Reference:
1. Walton
AH, Muenzer JT, Rasche D, Boomer JS, Sato B, et al. (2014) Reactivation of
Multiple Viruses in Patients with Sepsis. PLoS ONE 9(6): e98819.
doi:10.1371/journal.pone.0098819
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