Gene Therapy For The Heart - The SERCA Example

The push behind gene therapy for the heart is gaining strength alongside efforts to develop cell-mediated therapies to induce cardiomyocyte repair and regeneration (commented previously). Gene therapy strategies, particularly those based on viral vectors such as the adenoassociated virus (AAV) are attractive due to their relative ease of preparation and administration in preclinical models. One of the furthest along is AAV-mediated delivery of the sarco/endoplasmic reticulum Ca2+ ATPase pump (SERCA) for the treatment of heart failure.


The premise behind this approach lies in the observation that preclinical models of heart disease demonstrate a reduction in SERCA expression. Consequently, decreased SERCA activity in the cardiomyocytes may reduce the uptake of Ca2+ into the sarcoplasmic reticulum, and may therefore allow abnormal Ca2+ levels to persist during the cardiomyocyte’s Ca2+ oscillations. This may have implications for contractile activation / relaxation of the heart, and may even help to provoke a pro-hypertrophic response. The administration of an AAV encoding SERCA aims to counter these deleterious events by raising SERCA levels back to normal physiological levels.


To reasonably restore physiological SERCA function through AAV-mediated expression, it is instructive to keep in mind the basic and necessary steps of the AAV-mediated gene therapy paradigm. For the AAV-mediated therapy to have a reasonable chance at success, three general steps are requisites before we can reasonably hope to see clinical efficacy:


1. Inject virus at a dose sufficient to transduce the target organ

2. Assure that the virus meaningfully transduces the target organ

3. Check for *protein* expression in the target organ of interest


In regards to step 1: It is important to note that these are replication defective viral therapies. In that regard, there will be a proportionality between the target number of cells to be transfected and the viral dose. In simpler terms, the dose of virus required to meaningfully and reliably transduce a mouse heart will not be sufficient for equal transduction of a larger rat heart. Therefore, as we increase size of the target organ, the viral dose has to increase, thereby necessitating a scaling-up of doses as we move from mice to humans. Below is a graph showing the maximum viral genomes injected per gram of typical heart weight for the AAV-SERCA construct used by Celladon in clinical trials as well as the antecedent preclinical studies:


Arguably, there isn’t significant difference in dosing at the various stages. These data suggest that, given equal tropism of the virus for the heart across species, the dosing may be sufficient. Arguably, dosing in the preclinical sheep model was the highest, and would therefore give the best corollary for assessing the sufficiency of dosing in the clinic.


This allows us to move onto Step 2 and attempt to address the ability of the virus to transduce the target organ of interest. The most complete set of data provided in the available preclinical literature is from the sheep model described by Byrne et al. For an intracoronary dose of 2.5x10E13 viral genomes, they note the detection of an average of 1651 copies per ug of DNA from the heart, but that only 3 of the 6 injected animals had any detectable copies. In other words, 3 of 6 animals had no detectable persistence of the AAV, and of the 3 that did, they averaged 1651 copies per ug of DNA. For the liver and lung from these animals, they indicated the detection of 148773 copies and 7781 copies per ug of DNA, respectively. In essence, the data suggest that a minority of the injected AAV persists in the heart, if at all. Therefore, with respect to the targeting of the injected AAV to the intended organ, the preclinical sheep data imply that a significant challenge remains. If we assume that only the heart, lung and liver had detectable AAV and that they’re identically sized organs (Footnote 1), it would suggest an upper boundary of ~1% of the injected intracoronary dose targeted to the heart.


Nonetheless, the low level of AAV presence in the heart may be immaterial if a significant increase in SERCA protein can be demonstrated. To best address Step 3, we can examine the publication by Byrne et al to see if there are data provided for protein expression. Unfortunately, no Western blot data are provided. There is a vague indication about mRNA expression in the intracoronary versus intracoronorary + recirculation group, but it only indicates the degree of increase with recirculation versus without. Plus, mRNA expression does not guarantee protein expression, and without protein expression no therapeutic benefit can be expected or rationalized. However, given that only 3 of 6 animals receiving intracoronary injection of 2.5x10E13 viral genomes showed any persistence of the AAV whatsoever, we can safely assume that 50% of these animals had no increase in SERCA protein expression.


But what about the remaining 3 animals from the high dose intracoronary group? Absent explicit data from the authors, we can try to determine whether the resident viral genomes are present in sufficient number to elicit sufficient transcription / translation to increase SERCA protein levels. For these 3 animals, it was noted that they averaged 1651 copies of the AAV per ug of DNA. Therefore:


  • Convert the mass of DNA to mol basepairs: 1 ug DNA / (660 g/mol basepairs) = 1.52x10E-9 mol basepairs of DNA
  • Convert the mol of DNA bp into number of bp: 1.52 x 10-9 mol DNA bp * 6.02x10E23 basepairs/mol = 9.12x10E14 basepairs
  • Convert the number of basepairs into copies of the genome: For this step, we ride the assumption that the human genome is ~3x10^9 bp, meaning that 9.12x10^14 bp / (3x10^9 bp per genome) = 3.04x10E5 genomes.


Put simply, their test surveyed an equivalent of 304000 copies of the genome. Within those 304000 copies, 1651 copies of the exogenous AAV DNA were found. In other words, there were ~302350 copies of the endogenous SERCA gene and 1651 copies of the exogenously introduced SERCA. Therefore, the exogenous AAV-SERCA was responsible for increasing SERCA copies by ~0.5% over the amount endogenously present. Unfortunately, the clinical data does not appear to improve on the data from the preclinical sheep model. Szebo et al note that the highest level was 561 copies per ug of DNA assay from Patient ID 091007 (Table 3). Given similar calculations, that suggests an approximately 0.2% overexpression above endogenous levels. Suffice to say, that is not a large level of expression above and beyond what is already endogenously present.


The above calculations give us some insight into the consideration in Step 3: is there an increase in SERCA protein expression in the target organ of interest? The calculations regarding persistence of the AAV-SERCA would suggest that noticeable protein overexpression is unlikely. Therefore, we can comb through the preclinical work in rats, swine and sheep to determine if there is a consistent and reliable demonstration of increased SERCA protein in the heart of AAV transduced animals.


Sakata et al suggest increased AAV-mediated SERCA expression in a rat model of aortic banding (Fig. 4). However, there are no numerical data provided to document the extent or significance of overexpression, which is visually not striking. Further, a contemporaneous control using an AAV encoding for parvalbumin shows striking overexpression of parvalbumin protein, making the claimed SERCA overexpression appear modest, if at all significant. A thematically overlapping paper by the same group suggests a doubling of SERCA protein expression in the rat.


Moving to larger animals, a subsequent paper using a swine model suggests an increase in protein expression following AAV-SERCA administration in the heart failure group when compared to the saline treated heart failure group. Comparing the SERCA protein level in the AAV treated heart failure group to the normal, nonfailing group demonstrated no SERCA protein overexpression. Interestingly, these data are provided in bar graph form (Fig. 4) but are the only bar graphs in the manuscript that do not have error bars. In the sheep study reported by Byrne et al, no protein data are offered.


To be fair, Byrne et al note:


“Nevertheless, the positive functional effect of AAV2/1SERCA is entirely consistent with previous work that shows SERCA2a is a low-abundance gene and that only one to two functional copies are required per cell to maintain normal levels of SERCA mRNA and protein.”


This suggests that very little overexpression can have a significant functional impact. In that regard, it is important to note that the sheep receiving 2.5x10E13 viral genomes of AAV-SERCA by intracoronary infusion did not show improvement over control in any of the remodeling or functional parameters presented including left ventricular internal diameter (Fig. 2), change in fractional shortening or ejection fraction (Fig. 3), or positive or negative dP/dt (Fig. 4). Therefore, the low level of persistence for 2.5x10E13 viral genomes of AAV-SERCA administered through the intracoronary route in sheep did not translate into a functional benefit as presented, suggesting that the cited low threshold of expression required to restore normal SERCA protein was not exceeded.



All told, the high dose of 1x10E13 viral genomes administered in the trials to date by Celladon provide limited corroborating data to support the hypothesis that the functional outcomes are a result of AAV-mediated increases in myocardial SERCA expression. Although the CUPID clinical trial demonstrated a benefit for the 1x10E13 viral genome high dose group versus placebo, it is reasonable to ask, given the low level of persistence of the AAV-SERCA construct and scant data for increased SERCA protein expression, exactly what is the mechanism driving this benefit? The calculations and observations based on the preclinical models do not provide a consistent line of evidence for AAV-SERCA driven benefit. The ongoing CUPID2b study, administering 1x10E13 viral genomes via intracoronary route, will determine whether the functional outcomes in CUPID1 were reflective of the technology or a fortuitous coincidence within this patient group.







Footnote 1: The assumption that the heart, lung and liver are the same size benefits the calculations in favour of the heart. In fact, the liver is 4-5x larger by mass (~1.5 kg) and the lungs 2-3x larger by mass (~800 g) as per data here and here.