Smallpox pathophysiology
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: João André Alves Silva, M.D. [2]
Overview
Smallpox virus may be transmitted through contaminated surfaces or aerosolized particles. It is able to induce harm by evading the host's immune system and replicating inside host's cells. The virus may cause 3 forms of the disease: 1) ordinary; 2) flat-type; or 3) hemorrhagic smallpox. It infects different cells of the body, being known by it's characteristic lesions on the skin.
Transmission
Smallpox virus is transmitted by:[1]
- Physical contact
- Contact with infected body fluids
- Contact with infected objects
- Air through aerosolized particles
Genetics
Smallpox virulence is due to its ability to evade the host's immune system. Most proteins responsible for the pathogenesis of the virus are located at the terminal DNA regions of the virus.
Genetic comparisons of the smallpox virus with the vaccinia virus allowed to observe certain genetic changes that may be responsible for the virulence of the smallpox virus. However, without studying the gene's transcripts, it is not possible to draw objective conclusions.[2]
Pathogenesis
The smallpox virus commonly enters the body through the upper respiratory tract, invading the oropharyngeal and respiratory mucosa.[3] Other possible ports of entry include: skin, conjunctivae as well as through the placenta.[4] Although the viral scabs may contain life viruses, they are commonly contained within thickened material, which limits transmissibility.
Once in the respiratory mucosa, the infection commonly progresses as:[5][4][6]
- Asymptomatic respiratory mucosa infection
- Viral replication within respiratory epithelium
- Transient primary asymptomatic viraemia
- Virus enters macrophages and spreads to lymph nodes and reticuloendothelial system, where it replicates during 4 - 14 days
- Exuberant secondary viraemia, leading to symptom onset
During secondary viraemia the virus infects mucous cells of the pharynx and mouth, and endothelium of the capillaries of the dermis, causing skin scabs. Other organs with high viral loads include:[6]
Before development of the rash, the first lesions appear on the oropharyngeal mucosa, at which time the virus is released through the mucosal secretions, making that patient infectious.
Skin lesions develop due to migration of macrophages to the infected areas of the dermis, leading to edema and necrosis. With the influx of more polymorphonuclear cells, skin pustules will develop.[5]
The immune system responds to the viremia with activation of lymphocytes T and B and concomitant production of:[6]
- Neutralizing antibodies, during first week of disease, remaining for many years
- Hemagglutination-inhibition antibodies, by the 16th day of infection, beginning to decrease after 1 year
- Complement-fixation antibodies, by the 18th day of infection, beginning to decrease after 1 year
- Memory T cells, remaining for 50 years
Death by smallpox was commonly due to toxemia, following:[5]
Gross Pathology
Depending on the status of the patient's immune system, there may be identified 3 forms of smallpox:[7]
Ordinary Smallpox
Characterized by the following progression of lesions:[8]
- Initial hypopigmented macules, initially in the mouth
- Macules progress into papules and subsequently to vesicles
- Vesicles become pustules
- At the 14th day pustules loose liquid content and become crusted
- At the 3rd week, most crusts will separate (palms and soles last)
This form of smallpox is typical of an immunocompetent patient, whose immune system is able to inhibit viral replication.
Flat-type Smallpox
Characterized by the following progression of lesions:[9]
- Delayed appearance of macules
- Slow progression of the lesions, usually with flat and soft appearance
- Possible slough of skin sections
Most cases are fatal with presence of severe toxemia. This form of smallpox is typical of patients with weak cellular immune response to the virus.
Hemorrhagic-type smallpox
Characterized by the following progression of lesions:[10]
- Skin petechiae
- Mucous membrane and conjunctival bleeding
- Subcutaneous hemorrhage gives skin and conjunctivae deep red appearance
- Organ bleeding
- Early death by multi organ failure, usually before appearance of maculae.
This rare form of smallpox is typical of patients with severely compromised immune response, in which there is intense viral replication in the bone marrow and spleen It is also associated with intense toxemia.
Microscopic Pathology
The typical skin vesicles observed in smallpox occur following:[11]
- Viral infection of the epidermal cell
- Cells in malpighian layer enter balloon degeneration due to formation of vacuoles
- Cytoplasmic enlargement leads to loss of nuclear material
- Destruction of upper and middle layers of stratum spinosum
- Formation of vesicle, with high viral index
On the other hand, in the infected mucous surfaces, the viral proliferation and absence of the stratum corneum lead to the formation of ulcers. These ultimately lead to the release of greater loads of virus to the oropharynx.[12]
Histopathology
Poxviruses are characterized by cytoplasmic inclusions, however, these do not identify specifically the smallpox virus on a biopsy. There are 2 types of inclusion bodies:[13]
A-type
Typical of some viruses of the:
- Genus Orthopoxvirus:
- Cowpox virus
- Ectromelia virus
- Genus Avipoxvirus
B-type, or Guarnieri bodies
- Areas of active viral replication
- Present in infections by all poxviruses
- Appear as basophilic bodies near the nucleus on hematoxylin and eosin-stained samples
- Evident at epithelial cells underlying vesicles and pustules
Image Gallery
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Hematoxylin and eosin (H&E)-stained tissue sample, reveals some of the histopathologic changes found in a human skin tissue sample from the site of a smallpox lesion. Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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hematoxylin and eosin (H&E)-stained tissue sample, reveals some of the histopathologic changes found in a human skin tissue sample from the site of a smallpox lesion. Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
-
Upper arm revealing the site of a newly-administered smallpox vaccination, which had been performed using a “Ped-O-Jet®” jet injector. Notice the wheal type morphology of the vaccination site.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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This was a vaccinial lesion that had manifested itself on the face of a mother who had acquired the virus after her daughter’s smallpox vaccination.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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This is a chickenpox scab (left), and smallpox scab (right) viewed in profile as a demonstration in comparative morphology. Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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This image depicts the smallpox vaccination site, which in the case of this recipient, displayed a reaction after a period of seven days.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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This image depicts three mounted chickenpox scabs seen from the side revealing the superficiality of these scabs when morphologically compared to a smallpox scab.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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This image depicts the right shoulder region of a male patient from a lateral perspective, who’d received a smallpox vaccination, while ill with chickenpox. Note the intense reaction at the vaccination site.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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Viewed from above, this image depicts a smallpox scab (left), and chickenpox scab (right) as a demonstration in comparative morphology. Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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Classic maculopapular rash due to an ordinary, or “discrete” smallpox infection. Note distribution of the rash included his chest, left arm and hand, and left thigh and leg, affecting the contralateral side in the same manner.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
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African Cameroonian boy in the process of receiving his vaccinations during the African Smallpox Eradication and Measles Control Program.Adapted from Public Health Image Library (PHIL), Centers for Disease Control and Prevention.[14]
References
- ↑ "Smallpox disease overview".
- ↑ Massung RF, Liu LI, Qi J, Knight JC, Yuran TE, Kerlavage AR; et al. (1994). "Analysis of the complete genome of smallpox variola major virus strain Bangladesh-1975". Virology. 201 (2): 215–40. doi:10.1006/viro.1994.1288. PMID 8184534.
- ↑ Cecil, Russell (2012). Goldman's Cecil medicine. Philadelphia: Elsevier/Saunders. ISBN 1437716040.
- ↑ 4.0 4.1 "Smallpox and its Eradication" (PDF).
- ↑ 5.0 5.1 5.2 Moore, Zack S; Seward, Jane F; Lane, J Michael (2006). "Smallpox". The Lancet. 367 (9508): 425–435. doi:10.1016/S0140-6736(06)68143-9. ISSN 0140-6736.
- ↑ 6.0 6.1 6.2 Breman, Joel G.; Henderson, D.A. (2002). "Diagnosis and Management of Smallpox". New England Journal of Medicine. 346 (17): 1300–1308. doi:10.1056/NEJMra020025. ISSN 0028-4793.
- ↑ Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0443068399.
- ↑ Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0443068399.
- ↑ Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0443068399.
- ↑ Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0443068399.
- ↑ Cecil, Russell (2012). Goldman's Cecil medicine. Philadelphia: Elsevier/Saunders. ISBN 1437716040.
- ↑ Cecil, Russell (2012). Goldman's Cecil medicine. Philadelphia: Elsevier/Saunders. ISBN 1437716040.
- ↑ Mandell, Gerald (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases. Philadelphia, PA: Churchill Livingstone/Elsevier. ISBN 0443068399.
- ↑ 14.00 14.01 14.02 14.03 14.04 14.05 14.06 14.07 14.08 14.09 14.10 14.11 14.12 14.13 "Public Health Image Library (PHIL), Centers for Disease Control and Prevention".