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Volume 16, Number 7—July 2010

Dispatch

Postexposure Treatment of Marburg Virus Infection

Thomas W. GeisbertComments to Author , Lisa E. Hensley, Joan B. Geisbert, Anders Leung, Joshua C. Johnson, Allen Grolla, and Heinz Feldmann
Author affiliations: National Emerging Infectious Diseases Laboratories Institute, Boston, Massachusetts, USA (T.W. Geisbert, J.B. Geisbert); US Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland, USA (L.E. Hensley, J.C. Johnson); Public Health Agency of Canada, Winnipeg, Manitoba, Canada (A. Leung, A. Grolla); National Institutes of Health, Hamilton, Montana, USA (H. Feldmann)

Suggested citation for this article

Abstract

Rhesus monkeys are protected from disease when a recombinant vesicular stomatitis virus–based vaccine is administered 20–30 min after infection with Marburg virus. We protected 5/6 monkeys when this vaccine was given 24 h after challenge; 2/6 animals were protected when the vaccine was administered 48 h postinfection.

The filoviruses, Marburg virus (MBGV) and Ebola virus (EBOV), have been associated with sporadic episodes of hemorrhagic fever (HF) in Central Africa that produce severe disease and high mortality rates among infected patients (1). MBGV and EBOV are also considered potential biological weapons. No approved active or passive therapeutic modalities exist for filovirus infections. Although much progress has been made in developing preventive vaccines that can protect nonhuman primates against lethal challenge with MBGV and EBOV, advances in development of postexposure interventions against the filoviruses have not kept pace. Some degree of success has been achieved by using strategies that mitigate the coagulation abnormalities characterizing filoviral infection (2,3). Also, new postexposure treatment approaches, based on small interfering RNA (4) and antisense oligomers (5,6), have shown promising results in rodent models, but no reports have been published of evaluations of either strategy in the more stringent macaque models.

Recently, we showed the first complete postexposure protection of nonhuman primates against a filovirus by administering a live-attenuated recombinant vesicular stomatitis virus (rVSV) vaccine vector expressing the MBGV glycoprotein (GP) (VSVΔG MBGV GP) shortly after a high-dose MBGV challenge (7,8). We demonstrated that an rVSV vector, expressing the Zaire EBOV (ZEBOV) GP, protected 50% of rhesus macaques when administered shortly after a high-dose ZEBOV challenge (9). We further showed that an rVSV vector expressing the Sudan EBOV GP completely protected rhesus monkeys from a lethal challenge with this virus when administered shortly after exposure (10). All animals in these 3 studies were treated once with rVSV vectors 20–30 min after filovirus challenge. The primary question raised from these investigations is how far out treatment can be delayed before there is no survival or beneficial effect. Using a homologous VSVΔG MBGV GP vector, we have delineated a window of opportunity for treatment of MBGV-infected rhesus macaques.

The Study

Animal research was conducted in compliance with the Animal Welfare Act and other federal statutes and regulations relating to animals and experiments involving animals and adhered to the principles stated in the Guide for the Care and Use of Laboratory Animals, National Research Council, 1996. Fifteen healthy, filovirus-seronegative rhesus macaques (each weighing 4 kg–7 kg) were randomized into 2 experimental groups of 6 monkeys per group and 3 control groups of 1 animal per group. All 15 animals were challenged by intramuscular (IM) injection with 1,000 PFU of MBGV (Musoke strain). Approximately 24 h after MBGV challenge, animals in experimental group 1 received a single IM injection of VSVΔG MBGV GP (≈2 × 107 PFU) (8), and the animal in control group 1 received an equal dose of a VSV vector encoding a nonrelated GP (VSVΔG/LassaGPC). Approximately 48 h after MBGV challenge, animals in experimental group 2 received a single IM injection of VSVΔG MBGV GP (≈2 × 107 PFU), and the animal in control group 2 received an equal dose of VSVΔG/LassaGPC. The animal in control group 3 was not treated. Blood samples for viral infectivity titration, reverse transcription–PCR (RT-PCR), hematologic analysis, serum biochemical analysis, and immunoglobulin (Ig) G were collected before MBGV challenge and on days 3, 6, 10, 14, and 31–35 after MBGV challenge.

Figure

Thumbnail of Survival curves for Marburg virus–infected rhesus macaques treated 24 or 48 h after challenge with a recombinant vesicular stomatitis virus vaccine.

Figure. Survival curves for Marburg virus–infected rhesus macaques treated 24 or 48 h after challenge with a recombinant vesicular stomatitis virus vaccine.

Five of the 6 animals treated with VSVΔG/MBGV GP 24 h after MBGV challenge (animals 1, 2, 4–6) and 2 of the 6 animals treated with VSVΔG/MBGV GP 48 h after MBGV challenge (animals 7 and 10) survived (Figure; Appendix Table [PDF - 24 KB - 1 page]). In contrast, symptoms consistent with MBGV HF developed in 1 of the 6 macaques treated with VSVΔG/MBGV GP at 24 h (animal 3) and in 4 of the 6 animals treated with VSVΔG/MBGV GP at 48 h (animals 8, 9, 11, and 12); these included anorexia and a macular rash (Table 1). The 5 animals in which macular rash developed (animals 3, 8, 9, 11, and 12) also had plasma viremias >6.0 log10 PFU/mL by day 10; all 5 animals died during days 10–12 (Figure; Table 1; Appendix Table [PDF - 24 KB - 1 page]). Symptoms developed in control animals 1–3 consistent with MBGV HF; each had plasma viremia levels >7.0 log10 PFU/mL by day 10 and died on days 12, 12, and 11, respectively (Appendix Table [PDF - 24 KB - 1 page]).

Two of the 6 animals that survived MBGV challenge (animals 1 and 6) showed no change in appearance or behavior that indicated overt illness. Changes in hematologic results and/or blood parameters were observed in 5 of the surviving animals (2, 4, 5, 7, and 10) during the course of the study (Appendix Table [PDF - 24 KB - 1 page]). Plaque assay and RT-PCR were unable to detect any evidence of MBGV in the plasma of 6 of the 7 surviving animals (1, 2, 4–6, and 10). However, RT-PCR showed evidence of MBGV in peripheral blood mononuclear cells of 2 of these surviving animals (1 and 2) at day 10 (Table 2). Viremia of 4.2 log10 PFU/mL developed on day 10 in 1 surviving animal (7) treated 48 h after infection, and RT-PCR showed evidence of MBGV in peripheral blood mononuclear cells of this animal on days 6 and 10. Viremia in plasma was cleared, and the animal showed little evidence of illness by day 14. The serologic response profile of MBGV infection after treatment was evaluated by IgG ELISA. All 7 animals that were treated with VSV∆G/MBGV GP and survived infection showed moderate to high levels of IgG by day 14 (320–1,000); humoral response against MBGV was not detectable in the treated animals that died or in the control animals (Table 2).

Conclusions

This rhesus macaque model represents a worse-case scenario such as an accidental needle-stick exposure of a laboratory worker or first responder to a high infectious dose of a filovirus. Accidents such as these have occurred several times over the past 5 years (1113). Of direct relevance to our study was a recent laboratory accident in which an rVSV vector expressing the ZEBOV GP, which had been used successfully in postexposure treatment of experimentally infected nonhuman primates (9), was administered to a human ≈40 h after a ZEBOV needle-stick exposure (13). The patient received a dose of ≈5 × 107 PFU of the VSV ZEBOV GP vaccine, which is consistent with doses used in nonhuman primate studies (7,9,10). Fever, headache, and myalgia developed in the patient hours after injection but were successfully controlled with analgesics and antipyretics. Other adverse effects were not reported, but whether treatment was effective or whether the patient never became infected remains uncertain.

MBGV infection of humans normally progresses at a slower rate than does MBGV infection of macaques, with case-fatality rates in humans of 23%–90% (1) suggesting that the therapeutic window may be larger for humans than for infected macaques. In addition, the challenge dose that we employed in the rhesus monkey model of MBGV HF of 1,000 PFU represents >10,000 LD50 doses (14), again showing that this is a robust challenge model. In the current study, we achieved near complete protection from death when treatment with a single-dose regimen was delayed 24 h and 33% protection when treatment was delayed 48 h postexposure. Because no approved treatments exist for exposure to infectious filoviruses, the rVSV vectors described in the current study merit consideration for treating potential exposures and for further development for human use.

Dr Geisbert is the Associate Director of the National Emerging Infectious Diseases Laboratories Institute at Boston University, Boston, Massachussetts. His research focuses on emerging viruses with an emphasis on viruses causing hemorrhagic fever, including Ebola, Marburg, and Lassa viruses.

Acknowledgment

Funding was provided by the Defense Threat Reduction Agency, the Division of Intramural Research of the National Institute of Allergy and Infectious Diseases, National Institutes of Health, and the National Microbiology Laboratory of the Public Health Agency of Canada.

References

  1. Sanchez A, Geisbert TW, Feldmann H. Filoviridae: Marburg and Ebola viruses. In: Knipe DM, Howley PM, Griffin DE, Lamb RA, Martin, MA, Roizman B, et al., editors. Fields virology, 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2006. p. 1409–48.
  2. Geisbert TW, Hensley LE, Jahrling PB, Larsen T, Geisbert JB, Paragas J, Treatment of Ebola virus infection with a recombinant inhibitor of factor VIIa/tissue factor: a study in rhesus monkeys. Lancet. 2003;362:19538. DOIPubMed
  3. Hensley LE, Stevens EL, Yan SB, Geisbert JB, Macias WL, Larsen T, Recombinant human activated protein C for the postexposure treatment of Ebola hemorrhagic fever. J Infect Dis. 2007;196(Suppl 2):S3909. DOIPubMed
  4. Geisbert TW, Hensley LE, Kagan E, Zhaoying Yu E, Geisbert JB, Daddario-DiCaprio K, Postexposure protection of guinea pigs against a lethal Ebola virus challenge is conferred by RNA interference. J Infect Dis. 2006;193:16507. DOIPubMed
  5. Enterlein S, Warfield KL, Swenson DL, Stein DA, Smith JL, Gamble CS, VP35 knockdown inhibits Ebola virus amplification and protects against lethal infection in mice. Antimicrob Agents Chemother. 2006;50:98493. DOIPubMed
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  7. Daddario-DiCaprio KM, Geisbert TW, Stroher U, Geisbert JB, Grolla A, Fritz EA, Postexposure protection against Marburg haemorrhagic fever with recombinant vesicular stomatitis virus vectors in non-human primates: an efficacy assessment. Lancet. 2006;367:1399404. DOIPubMed
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  9. Feldmann H, Jones SM, Daddario-Dicaprio KM, Geisbert JB, Stroher U, Grolla A, Effective post-exposure treatment of Ebola infection. PLoS Pathog. 2007;3:e2. DOIPubMed
  10. Geisbert TW, Daddario-Dicaprio KM, Williams K, Geisbert JB, Leung A, Feldmann F, Recombinant vesicular stomatitis virus vector mediates postexposure protection against Sudan Ebola hemorrhagic fever in nonhuman primates. J Virol. 2008;82:56648. DOIPubMed
  11. International Society for Infectious Diseases. Ebola, lab accident death—Russia (Siberia) [cited 2004 May 22]. http://www.promedmail.org, archive no. 20040522.1377.
  12. Kortepeter MG, Martin JW, Rusnak JM, Cieslak TJ, Warfield KL, Anderson EL, Managing potential laboratory exposure to Ebola virus by using a patient biocontainment care unit. Emerg Infect Dis. 2008;14:8817. DOIPubMed
  13. Tuffs A. Experimental vaccine may have saved Hamburg scientist from Ebola fever. BMJ. 2009;338:b1223. DOIPubMed
  14. Gonchar NI, Pshenichnov VA, Pokhodiaev VA, Lopatov KL, Firsova IV. The sensitivity of different experimental animals to Marburg virus. Vopr Virusol. 1991;36:4357.PubMed

Figure

Tables

Suggested citation for this article: Geisbert TW, Hensley LE, Geisbert JB, Leung A, Johnson JC, Grolla A, et al. Postexposure treatment of Marburg virus infection. Emerg Infect Dis [serial on the Internet]. 2010 Jul [date cited]. http://wwwnc.cdc.gov/eid/article/16/7/10-0159

DOI: 10.3201/eid1607.100159

Table of Contents – Volume 16, Number 7—July 2010

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Thomas W. Geisbert, Boston University School of Medicine, National Emerging Infectious Diseases Laboratories Institute, 620 Albany St, Rm 401B, Boston, MA 02118, USA

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