The Antiherpesvirus Activity of H2G [(R)-9-[4-Hydroxy-2-(Hydroxymethyl)Butyl]Guanine] Is Markedly Enhanced by the Novel Immunosuppressive Agent Mycophenolate Mofetil

Mycophenolate mofetil (MMF), the morpholinoethyl ester of mycophenolic acid (MPA) is an immunosuppressant that is currently used in kidney transplant recipients. After oral administration, MMF is hydrolyzed to MPA, the active immunosuppressive agent, which is a potent inhibitor of IMP dehydrogenase. IMP dehydrogenase is responsible for the conversion of IMP through XMP to GMP. Since IMP represents an important intermediate in the generation of nucleotides containing guanine as the base, MPA will cause depletion of the intracellular guanine nucleotide pools (Fig. 1). The immunosuppressive effect of MPA has been ascribed to this depletion of the dGTP pools (13, 19, 21, 23, 25).

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Fig. 1.

Proposed mechanism by which MPA and ribavirin potentiate the antiherpesvirus activity of H2G. For further information on (i) the phosphorylation of H2G, see reference 14; (ii) the inhibition of viral DNA polymerases by H2G-TP, see references2 and 14; (iii) the phosphorylation of ribavirin, see reference 26; and (iv) the inhibition of IMP dehydrogenase by MPA and ribavirin monophosphate, see references 19, 23, and26. MP, monophosphate; DP, diphosphate; TP, triphosphate; Ado, adenosine.

H2G ([(R)-9-[4-hydroxy-2-(hydroxymethyl)butyl]guanine] is an acyclic purine nucleoside analog with activity against herpesviruses, including herpes simplex virus types 1 (HSV-1) and 2 (HSV-2), Epstein-Barr virus, human herpesviruses 6 (HHV-6) and 8 (HHV-8), and particularly varicella-zoster virus (VZV) (1-4, 16, 17, 24). H2G is converted to its monophosphate form by the HSV-1-, HSV-2-, or VZV-encoded thymidine kinase and is then further phosphorylated to its triphosphate form (H2G-TP), which selectively inhibits the viral DNA polymerase. H2G-TP inhibits HSV-1, HSV-2, and VZV DNA polymerases competitively with dGTP (atK_is of 2.8, 2.2, and 0.3 μM, respectively), but it does not serve as an alternative substrate in the polymerization reaction (16). The compound has recently entered phase I/II clinical trials for the treatment of herpesvirus infections, in particular with VZV infections.

We recently showed that the antiherpesvirus activity of acyclovir (ACV), penciclovir (PCV), and ganciclovir (GCV), which, like H2G, are acyclic guanosine nucleoside analogs, is markedly stimulated by MPA and its oral prodrug MMF (18). MMF and MPA are themselves virtually inactive against herpesviruses (with the exception of human cytomegalovirus [CMV], which is slightly inhibited by MPA). ACV, PCV, and GCV, like H2G, are specifically phosphorylated by virus-encoded kinases (HSV-1-, HSV-2-, and VZV-encoded thymidine kinase for all four compounds and, in addition, CMV-encoded UL97 kinase for GCV) to their monophosphate forms and, further on, by cellular kinases to the triphosphate form (11). The triphosphates are specific and strong inhibitors of the viral DNA polymerases. We have demonstrated that a depletion of the dGTP pools brought about by MPA is responsible for the potentiating effect of MPA on the antiherpesvirus activity of ACV, PCV, and GCV (18).

Similarly, ribavirin has been shown to potentiate the anti-HIV activity of 2′3′-dideoxyinosine and other purine nucleoside analogs with anti-HIV activity (7, 8, 13, 14). The increased IMP pools in the ribavirin-treated cells were found to result in an increased phosphorylation of 2′,3′-dideoxyinosine by 5′-nucleotidase, an enzyme that uses IMP as the phosphate donor (9). We have demonstrated that this mechanism does not hold for ACV and GCV (18), although these molecules have been shown to act as a substrate for 5′-nucleotidase (15).

In the present study, we assessed whether MPA also potentiates the antiherpesvirus activity of H2G. Since this compound is currently under clinical study for the therapy of herpesvirus infections, in the future it may well be used concomitantly with the immunosuppressant MMF in those transplant recipients that develop opportunistic herpesvirus infections as a result of the immunosuppressive action of MMF.

Human embryonic lung (HEL) cells and Vero cells were propagated in minimal essential medium (MEM) supplemented with 10% fetal calf serum,l-glutamine, and bicarbonate. Human CMV (strain Davis) and VZV (strains OKA, 07-1, and YS-R) were obtained from the American Type Culture Collection. The origin of HSV-1 (strain KOS) and HSV-2 (strain G) and thymidine kinase-deficient (TK⁻) HSV-1 (B2006) have been described before (12). Biochemical evidence that the B2006, 07-1, and YS-R strains are TK deficient was obtained from phosphorylation studies with radiolabelled ACV. Levels of the triphosphate form of ACV (ACV-TP) in Vero cells infected with the HSV-1 TK⁻ strain (B2006) were 2.7% of the levels in cells infected with the wild-type virus. The levels of ACV-TP in HEL cells infected with the YS-R and 07-1 strains were ≤3.6% (detection limit) of the levels in cells infected with the wild-type virus.

H2G was kindly provided by A. Molla (Abbott Laboratories, Abbott Park, Ill.), MPA and guanosine were from Sigma (St. Louis, Mo.), and ribavirin was from ICN (Costa Mesa, Calif.). [8-³H]ACV (specific activity, 15 Ci/mmol) was from Moravek Biochemicals (Brea, Calif.). Confluent cultures of Vero cells grown in microtiter trays were inoculated with 100 times the 50% cell culture infective dose of the different HSV strains, whereas confluent cultures of HEL cells were inoculated with 100 PFU of CMV or 20 PFU of VZV. Compounds, either alone or in combination, were added after a 2-h virus adsorption period. Virus-induced cytopathic effect (CPE) was recorded microscopically at 2 to 3 days postinfection (p.i.) for the HSV strains and at 7 days p.i. for CMV. VZV-induced plaque formation was evaluated at 5 days p.i. The 50% effective concentrations (EC₅₀s) were derived from graphical plots.

Cytostatic effects were monitored in Vero cells (in MEM containing 20% fetal calf serum) that were seeded at a density of 4,000 cells/well in 96-well plates and were allowed to attach to the plastic for 24 h. Thereafter, serial dilutions of the test compounds (in MEM containing 2% fetal calf serum), either alone or in combination, were added. The cells were further incubated for 3 days at 37°C, at which time they were trypsinized and counted with a Coulter Counter.

To determine the effect of MPA on intracellular GTP pools, 1-day-old confluent cultures of Vero cells were incubated with different concentrations of MPA for 48 h. After two washes in phosphate-buffered saline, the cells were collected by trypsinization and nucleotides were extracted in 70% ice-cold methanol. Quantification of nucleotide pools was done by high-performance liquid chromatography analysis using a Partisil-sphere radial-compression column (Pharmacia, St. Albans, Hertsfordshire, United Kingdom) as described previously (5). To quantify the levels of ACV-TP generated in cells that had been infected with the different HSV or VZV strains, radiolabeled ACV was added for 24 h at the time that the CPE was ≈60%. Samples were analyzed by high-performance liquid chromatography, and radioactivity in the different fractions was determined by means of liquid scintillation counting.

H2G potently inhibited the replication of HSV-1 and HSV-2 but had, as expected, little or no effect on the replication of the TK⁻ HSV-1 strain (Table 1). At the concentrations used (10, 2.5, 1, and 0.25 μg/ml), MPA had virtually no inhibitory effect on the CPE progression in the HSV-1-, HSV-2-, and TK⁻ HSV-1-infected cultures. However, when H2G was combined with MPA, a pronounced enhancement of the antiviral activity of H2G was noted. In fact, the EC₅₀ of H2G for inhibition of HSV-1 and HSV-2 replication decreased 100- to 150-fold. Of special interest is our observation that H2G, when combined with MPA, efficiently inhibited the replication of the TK⁻strain of HSV-1. In this case, the increase in antiviral activity was over 2,500-fold. Thus, the EC₅₀ of H2G for inhibition of replication of the TK⁻ HSV-1 strain dropped from values that are not attainable in plasma (>100 μg/ml) to values that could be easily reached (0.04 to 0.8 μg/ml). This pronounced potentiating effect can be explained only by the formation of small amounts of phosphorylated products of H2G in cells infected with the TK⁻ virus. This is most likely accomplished by the residual activity of the defective viral TK, or, alternatively, by cellular TK, or by both. Similar to our findings with HSV, MPA also had a pronounced potentiating effect on the anti-VZV activity of H2G (Table1). H2G was about 1,000-fold less effective against the TK⁻ strains of VZV (07-1 and YS-R) than against the wild-type strains (OKA and YS). However, when combined with MPA, again at concentrations attainable in plasma, these TK⁻ strains became up to 60-fold more sensitive to H2G.

The potentiating effects of MPA on the antiviral activity of H2G against HSV-1, HSV-2, and TK⁻ HSV-1 were efficiently reversed upon addition of guanosine to the culture medium (Table2). Under the conditions used, MPA also markedly depleted the GTP pools in these cells. Levels of GTP (percent) were 22 ± 4, 37 ± 0.7, 32 ± 9, and 45 ± 6 (mean ± standard deviation) in confluent Vero cell cultures that had been incubated for 48 h with, respectively, 10, 2.5, 1, and 0.25 μg of MMF per ml in comparison to the levels of GTP in untreated control cultures. Our findings thus indicate that the observed potentiating effect of MPA on the antiviral activity of H2G, as shown previously for ACV, PCV, and GCV, must be explained by a depletion of the guanine nucleotide pools, resulting in a decreased competition of dGTP with H2G-TP in the viral DNA polymerization reaction.

In contrast to ACV, GCV, and PCV (18), H2G did not gain a synergistic increase in its already weak anti-CMV activity when combined with MMF (data not shown). This may indicate that (i) virtually no phosphorylated metabolites of H2G are formed in the CMV-infected cells and/or that (ii) H2G-TP is a (very) poor inhibitor of the CMV-encoded DNA polymerase. MMF had by itself some inhibitory effect on CMV replication (EC₅₀, ≈2.5 μg/ml). The anti-CMV activity of azathioprine, another immunosuppressive agent, has been described before (22).

To confirm the observations made for MPA, we also studied the antiherpesvirus activity of the combination of H2G and ribavirin. Ribavirin is a broad-spectrum antiviral agent that has virtually no activity against herpesviruses (20). In its monophosphate form, ribavirin, like MPA, acts as a potent inhibitor of IMP dehydrogenase and thus also causes depletion of the intracellular guanine nucleotide pools (Fig. 1). Similarly to MPA, ribavirin also markedly potentiates the activity of H2G against HSV-1 (10-fold), HSV-2 (10-fold), and TK⁻ HSV-1 (185-fold), although ribavirin did so less efficiently than MPA (Table3). Ribavirin alone had no activity against the viruses studied. The reason for ribavirin not being as efficient as MPA in potentiating the antiviral activity of H2G can be explained by the fact that ribavirin monophosphate is a less potent inhibitor of IMP dehydrogenase than is MPA (6).

Finally, we wanted to determine whether the combination of H2G and MPA or H2G and ribavirin increased the cytostatic action of H2G. As can be derived from Fig. 2, H2G alone had only a limited cytostatic effect (i.e., a 30 to 40% reduction of Vero cell growth at 50 μg/ml). Addition of MPA or ribavirin at concentrations around their 50% cytostatic concentration for Vero cell growth resulted in an additive, rather than a synergistic, inhibition of cell growth. Similarly, we also observed no potentiation of the cytostatic action of GCV when it was combined with MPA (18). Although we did not observe any stimulation in the cytostatic action of H2G when combined with MPA, we suggest that patients receiving MMF be carefully monitored for a potential increase in the side effects of H2G.

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Fig. 2.

Effect of MPA (A) and ribavirin (B) on the cytostatic action of H2G on Vero cells. Data are mean values for at least two separate experiments.

In conclusion, MPA strongly enhances the anti-HSV and anti-VZV activities of the novel purine nucleoside analog H2G. The concentrations required for MPA to potentiate the antiviral activity of H2G do not have to exceed 1 μg/ml, i.e., a concentration that is even below the MPA concentration attained in plasma upon oral dosing of 0.5 to 3 g of MMF (10). The mechanism of action resides in a depletion by MPA of the intracellular dGTP pools, thus favoring the inhibitory effect of H2G-TP on the viral DNA polymerase. Since clinical trials of the efficacy of H2G against herpesvirus infections are currently underway, it will be of interest to investigate whether the antiviral efficacy of H2G is enhanced in patients that are undergoing immunosuppressive therapy with MMF. The use of MMF in transplant recipients may thus be considered a double-edged sword. On the one hand, it may precipitate the reactivation of opportunistic herpesviruses. On the other hand, once the patient receives H2G for this infection, the synergistic action between the two compounds may compensate for the increased risk of developing herpesvirus infections.

• Copyright © 1998 American Society for Microbiology