Table 1.
Date(s) | Blood result |
Cerebrospinal fluid result |
Antiviral treatment |
|||||||
---|---|---|---|---|---|---|---|---|---|---|
CMV PCRb | Amino acid change associated with CMV resistance to antiviral drugsf |
CMV PCRb | Amino acid change associated with CMV resistance to antiviral drugs |
Drug(s) | Duration | |||||
Date | UL97 PTc | UL54 DPd | Date | UL97 PTc | UL54 DPd | |||||
July 2008–June 2009 | − | − | Oral ACV | 11 mos | ||||||
June 2009 | + (3.9 → <2.7) | − | GCV | 2 wks | ||||||
June–July 2009 | − | Oral ACV | 4 wks | |||||||
July–August 2009 | + (3.2 → 5.4) | FOS | 3 wks | |||||||
August–September 2009 | + (5.4 → 3.9) | FOS + GCV | 3 wks | |||||||
September–December 2009 | + (3.9 → 3.6) | November 2009 | 0 | 0 | CDV + GCV | 14 wks | ||||
December 2009 | + (3.6 → 5.8) | FOS + GCV | 2 wks | |||||||
December 2009–January 2010 | + (5.8 → <2.7) | FOS + GCV + artesunate | 4 wks | |||||||
January–March 2010 | − | VGCV | 2 mos | |||||||
March–April 2010 | + (2.9 → 4.4) | VGCV | 2 mos | |||||||
May 2010 | + (4.4 → <2.7) | May 2010 | M460I | L545S | FOS + GCV | 2 wks | ||||
June 2010–January 2011 | − | VGCV | 7 mos | |||||||
January 2011 | + (3.3 → <2.7) | January 2011 | 0 | 0 | FOS | 2 wks | ||||
January–September 2011 | − | VACV | 9 mos | |||||||
September–October 2011 | − | + (3.8 → 3.9) | September 2011 | H520Q | L545S | FOS + GCV | 5 wks | |||
October–November 2011 | − | + (3.9 → 4.9) | VACV | 9 wks | ||||||
November 2011–June 2012 | + (3.4 → 3.7) | February 2012e | 0 | 0 | + (4.9 → 4.3) | February 2012 | H520Q | L545S | VACV | 7 mos |
February 2012e | H520Q | L545S | ||||||||
May 2012 | M460I | L545S | ||||||||
June–August 2012 (death) | + (3.7 → 5.3) | June 2012 | M460I | L545S | + (4.3 → 3.2) | FOS + GCV | 5 wks |
CMV, cytomegalovirus; UL97 PT, UL97 phosphotransferase; UL54 DP, UL54 DNA polymerase; ACV, acyclovir; GCV, intravenous ganciclovir; FOS, foscarnet; CDV, cidofovir; VGCV, valganciclovir; VACV, valaciclovir; i.v., intravenous.
In cases of positive CMV PCR results, results of the PCR at the initiation and at the end of each antiviral regimen are indicated in parentheses (expressed in log10 copy numbers/ml).
In all genotypic resistance tests, the following amino acid changes relative to natural polymorphisms of CMV UL97 phosphotransferase were isolated: Q19E, N68D, S108N, and I244V.
In all genotypic resistance tests, the following amino acid changes relative to the natural polymorphism of CMV UL54 DNA polymerase were isolated: A885T and N898D.
Genotypic resistance tests were performed using the same blood sample (the second test has been retrospectively assessed).
A “0” entry indicates that no amino acid change was evidenced.