Human Monkeypox (MPX) is a zoonosis which presents with a smallpox-like disease. MPX was named for its initial identification in 1958 in a group of monkeys transported to Copenhagen, Denmark, from Africa.
MPX is caused by the monkeypox virus (MPXV), an enveloped double-stranded DNA virus that is a member of the genus Orthopoxvirus. Other members of Orthopoxvirus include variola (smallpox), vaccinia, cowpox virus, camelpox virus, and ectromelia virus (mousepox). MPXV is, in a sense, a misnomer: although initially identified in monkeys, the reservoir species for MPXV is thought to be an unidentified species of rodent (possibly Gambian pouched rat, rope squirrel, or other rodent). Transmission is by broken skin, droplets, or bodily fluids. Sexual activity is thought to be either a route of transmission or may amplify transmission. The incubation period for the virus is 7–14 days most frequently but has been reported to be up to 3 weeks.
There are two clades of MPXV, a West African (WA) clade and a Congo Basin (CB) clade. MPX disease caused by the CB clade may have greater mortality, morbidity, viremia, and transmission relative to disease caused by the WA strain.
Countries which are endemic for MPX include: Cameroon, the Central African Republic, the Democratic Republic of the Congo, Gabon, Ghana (identified in animals only), Cote d’Ivoire, Liberia, Nigeria, the Republic of the Congo, and Sierra Leone. MPX is rare outside of endemic countries, but in 2003, an outbreak occurred in the United States related to MPXV-infected prairie dogs.
Since May 2022, there has been an ongoing international outbreak of MPX which includes nonendemic countries. As of July 29, 2022, there have been 22,485 cases of which the greatest number of cases are in the United States (4906 cases), Spain (4298 cases), Germany (2595 cases), United Kingdom (2546 cases), and France (1955 cases).
Outbreaks in endemic countries have revealed the following risk factors for MPX infection: lack of smallpox vaccination; living in forested area; male sex; age less than 15 years; and consumption of bushmeat.
The 2022 global outbreak has shown a disproportionate occurrence in men who have sex with men (MSM), which has not been noted in previous outbreaks. Although a majority of cases in the 2022 outbreak have been in adult men (especially MSM), cases in women and in children have also been reported. Incident cases commonly had a history of travel (most frequently to Europe) in the month prior to onset of symptoms.
Dermatopathology shows similar histologic findings to vaccinia and cowpox virus. Guarnieri bodies, characteristic of poxviruses, are present in skin keratinocytes. Other pathologic features may include proliferation of basal keratinocytes, epidermal necrosis and spongiosis, keratinocyte pallor, and dense inflammatory cell infiltrate with vasculitis.
Data from previous outbreaks have shown that smallpox vaccination provides 85% protection against MPX. In the United States, there are two currently available smallpox vaccines that may provide protection against MPX. ACAM2000 utilizes replication-competent vaccinia virus, and is administered by percutaneous skin scarification in a single dose. JYNNEOS is a newer vaccine preparation which contains a replication-deficient vaccinia virus and is administered subcutaneously in two doses. These vaccines are available in the United States for pre-exposure prophylaxis in certain high-risk occupational groups, and for postexposure prophylaxis. The JYNNEOS vaccine is becoming increasingly available, and local/regional departments of public health have information on how vaccines are being distributed in any particular area.
Patients may provide a history of contact with a known MPX case. There may be a history of recent travel to MPX-endemic countries (West or Central Africa) or to nonendemic countries where the present outbreak is ongoing. Given the current outbreak’s possible sexual transmission, it is prudent to inquire about sexual practices, new sexual partners, or whether sexual partners are experiencing symptoms.
The skin lesions progress through the following stages in order: macule, papule, vesicle, pustule, crusting, and scar. Lesions on the same part of the body are typically in the same stage. Classically, the distribution of skin lesions in MPX is centrifugal and may be most dense on the face, trunk, and extremities. As the skin lesions may occur on the face, the eyelids may be involved. In the 2022 outbreak, the anogenital area has been the most common site for skin lesions (73% of patients).
Mucosal lesions may also occur and may affect oropharyngeal, nasal, genital, and ocular mucosa. When the ocular surface is affected, blepharoconjunctivitis and ulcerative keratitis may occur. In a 1981-1986 CB clade outbreak of MPX, the rate of “blepharitis and conjunctivitis” was 30% in smallpox-unvaccinated patients and 7% in smallpox-vaccinated patients. Ulcerative keratitis was reported to occur in 3%–4% of MPX cases in a CB outbreak. The precise frequency of ocular MPX manifestations in the 2022 outbreak is not yet known. In a retrospective series by Thornhill et al, conjunctival lesions were reported in 3/528 patients (0.6%), but this retrospective analysis may have underestimated the true occurrence.
Systemic sequelae may include bronchopneumonia and respiratory distress, gastrointestinal involvement with vomiting and diarrhea, encephalitis, and secondary bacterial infections and sepsis. Lymphadenopathy is a clinical feature that distinguishes MPX from smallpox.
Ancillary testing to confirm diagnosis is performed by swabbing skin lesions. The swabs may be sent for nucleic acid amplification testing by real-time or conventional polymerase chain reaction.
- Chickenpox (varicella)
- Herpes simplex
- Molluscum contagiosum
- Shingles (herpes zoster)
- Smallpox (variola)
MPX course is usually self-limited, so treatment is frequently supportive only. Patients with severe disease or at risk for developing severe disease may be treated with systemic antiviral agents, which include tecovirimat, cidofovir, brincidofovir, and intravenous vaccinia immune globulin may be utilized for systemic treatment. Antiviral agents are available in the United States through state/regional health departments and the Centers for Disease Control and Prevention. Hospitalization may be needed.
Treatment of ocular disease
Aggressive lubrication has historically been used for treatment of ocular manifestations of orthopoxvirus infections including by MPXV. Topical antibiotics may be necessary for prophylaxis of epithelial defects or for bacterial superinfection. Trifluridine has been used for ocular manifestations of the closely related virus vaccinia. In severe cases, corneal transplantation may be needed for perforation or for visual rehabilitation.
The typical duration of symptoms and signs of MPX is 2–5 weeks. As noted above, the course of MPX is usually self-limited. Skin lesions may lead to scarring, especially when scratched. The lesions may appear atrophic and may be either hypo- or hyper-pigmented. The historical case fatality rate from prior outbreaks is 10.6% in the CB clade and 3.6% in the WA clade. In the 2022 outbreak, the mortality rate appears to be lower: in the retrospective series by Thornhill et al, of 528 cases no deaths were reported.
Affected individuals are advised to isolate at home to minimize transmission. They are advised to remain in isolation until scabs have fallen off, the rash has fully healed, and new intact skin has formed. Contact with other persons and with pets or animals should be avoided. Commonly touched surfaces should be cleaned and disinfected, and potentially contaminated items (including linens and eating/drinking utensils) should not be shared.
In the healthcare setting, a suspected or known case should be placed in a single-person room with the door closed, and movement beyond the room minimized. Healthcare providers should wear personal protective equipment including a gown, gloves, eye protection that covers the front and side of the face, and a particulate respiratory mask with an N95 filter or higher. Surfaces should be cleaned, using an United States Environmental Protection Agency (EPA)-registered hospital-grade disinfectant with an emerging viral pathogen claim, a claim that is regulated by the EPA. For eyecare providers, it may be prudent to utilize slit lamp shields as a barrier. Detailed guidance for infection prevention both at home and in the healthcare setting are available on the CDC website.
It is not known if monkeypox can be transmitted through cadaveric corneal transplantation, as no such cases have been reported. Studies in infected rodents suggest conjunctival shedding of MPXV, so the possibility for transmission in humans via cadaveric corneal transplantation is theoretically plausible if viral shedding occurs similarly in humans. Because MPXV is an enveloped virus, it should be susceptible to povidone-iodine disinfection. The Eye Bank Association of America (EBAA) recommended exclusion of potential donors who in the last 21 days developed a rash characteristic of MPX, had a close contact with a confirmed MPX infection, tested positive for MPXV, or tested positive for Orthopoxvirus.
- Centers for Disease Control and Prevention (CDC) webpage about monkeypox
- World Health Organization (WHO) webpage about monkeypox
- Eye Bank Association of American (EBAA) webpage with Monkeypox Informational Alert
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