| Epstein–Barr virus infection |
| Classification and external resources |
| ICD-9 |
075 |
| OMIM |
226990 |
| MeSH |
D020031 |
There are several forms of Epstein–Barr virus infection. Infectious mononucleosis, nasopharyngeal carcinoma, and Burkitt's lymphoma can all be caused by the Epstein–Barr virus.
Contents
- 1 Pathology
- 1.1 Infectious mononucleosis
- 1.2 EBV-associated malignancies
- 2 Clinical symptoms
- 3 Treatment
- 4 EBV-associated diseases
- 5 See also
- 6 References
Pathology
Infectious mononucleosis
Epstein–Barr can cause infectious mononucleosis, also known as 'glandular fever', 'Mono' and 'Pfeiffer's disease'. Infectious mononucleosis is caused when a person is first exposed to the virus during or after adolescence. Though once deemed "The Kissing Disease," recent research has shown that transmission of EBV not only occurs from exchanging saliva, but also from contact with the airborne virus.[citation needed] It is predominantly found in the developing world, and most children in the developing world are found to have already been infected by around 18 months of age. Infection of children can occur when adults mouth feed or pre-chew food before giving it to the child.[1] EBV antibody tests turn up almost universally positive. In the United States roughly half of five-year-olds have been infected,.[2]
EBV-associated malignancies
This photomicrograph depicts leukemia cells that contain Epstein Barr virus using a FA staining technique. Epstein–Barr virus, EBV, is a member of the Herpesvirus family, and is one of the most common human viruses. When infection with EBV occurs during adolescence or young adulthood, it causes infectious mononucleosis 35% to 50% of the time. (CDC)
The strongest evidence linking EBV and cancer formation is found in Burkitt's lymphoma and nasopharyngeal carcinoma. Additionally, it has been postulated to be a trigger for a subset of chronic fatigue syndrome patients[3] as well as multiple sclerosis and other autoimmune diseases.[4]
Burkitt's lymphoma is a type of Non-Hodgkin's lymphoma and is most common in equatorial Africa and is co-existent with the presence of malaria.[5] Malaria infection causes reduced immune surveillance of B cells immortalized by EBV, resulting in an excessive number of B cells and an increased likelihood of an unchecked mutation. Repeated mutations can lead to loss of cell-cycle control, causing excessive proliferation observed as Burkitt's lymphoma. Burkitt's lymphoma commonly affects the jaw bone, forming a huge tumor mass. It responds quickly to chemotherapy treatment, namely cyclophosphamide, but recurrence is common.
Other B cell lymphomas arise in immunocompromised patients such as those with AIDS or who have undergone organ transplantation with associated immunosuppression (Post-Transplant Lymphoproliferative Disorder (PTLPD)). Smooth muscle tumors are also associated with the virus in malignant patients.[6]
Nasopharyngeal carcinoma is a cancer found in the upper respiratory tract, most commonly in the nasopharynx, and is linked to the EBV virus. It is found predominantly in Southern China and Africa, due to both genetic and environmental factors. It is much more common in people of Chinese ancestry (genetic), but is also linked to the Chinese diet of a high amount of smoked fish, which contain nitrosamines, well known carcinogens (environmental).[7]
Clinical symptoms
Symptoms of infectious mononucleosis are fever, sore throat, and swollen lymph glands. Sometimes, a swollen spleen or liver involvement may develop. Heart problems or involvement of the central nervous system occurs only rarely, and infectious mononucleosis is almost never fatal. There are no known associations between active EBV infection and problems during pregnancy, such as miscarriages or birth defects.[8][9] Although the symptoms of infectious mononucleosis usually resolve in 1 or 2 months, EBV remains dormant or latent in a few cells in the throat and blood for the rest of the person's life. Periodically, the virus can reactivate and is commonly found in the saliva of infected persons. Reactivated and post-latent virus may pass the placental barrier in (also seropositive) pregnant women via macrophages and therefore can infect the fetus. Also re-infection of prior seropositive individuals may occur. In contrast, reactivation in adults usually occurs without symptoms of illness.
EBV also establishes a lifelong dormant infection in some cells of the body's immune system. A late event in a very few carriers of this virus is the emergence of Burkitt's lymphoma and nasopharyngeal carcinoma, two rare cancers. EBV appears to play an important role in these malignancies, but is probably not the sole cause of disease.
Most individuals exposed to people with infectious mononucleosis have previously been infected with EBV and are not at risk for infectious mononucleosis. In addition, transmission of EBV requires intimate contact with the saliva (found in the mouth) of an infected person. Transmission of this virus through the air or blood does not normally occur. The incubation period, or the time from infection to appearance of symptoms, ranges from 4 to 6 weeks. Persons with infectious mononucleosis may be able to spread the infection to others for a period of weeks. However, no special precautions or isolation procedures are recommended, since the virus is also found frequently in the saliva of healthy people. In fact, many healthy people can carry and spread the virus intermittently for life. These people are usually the primary reservoir for person-to-person transmission. For this reason, transmission of the virus is almost impossible to prevent.
The clinical diagnosis of infectious mononucleosis is suggested on the basis of the symptoms of fever, sore throat, swollen lymph glands, and the age of the patient. Usually, laboratory tests are needed for confirmation. Serologic results for persons with infectious mononucleosis include an elevated white blood cell count, an increased percentage of certain atypical white blood cells, and a positive reaction to a "mono spot" test.
Treatment
There is no specific treatment for infectious mononucleosis, other than treating the symptoms. No antiviral drugs or vaccines are available. Some physicians have prescribed a 5-day course of steroids to control the swelling of the throat and tonsils. The use of steroids has also been reported to decrease the overall length and severity of illness, but these reports have not been published.[citation needed]
It is important to note that symptoms related to infectious mononucleosis caused by EBV infection seldom last for more than 4 months. When such an illness lasts more than 6 months, it is frequently called chronic EBV infection. However, valid laboratory evidence for continued active EBV infection is seldom found in these patients. The illness should be investigated further to determine if it meets the criteria for chronic fatigue syndrome, or CFS. This process includes ruling out other causes of chronic illness or fatigue.
EBV-associated diseases
- Hodgkin's disease
- Acute renal failure[10]
- Alice in Wonderland syndrome
- Common variable immunodeficiency (CVID)
- Hairy leukoplakia
- Hepatitis
- Herpangina
- Infectious mononucleosis
- Kikuchi's disease
- Multiple Sclerosis (higher risk in patients infected as teenagers than as children)
- Nasopharyngeal cancer
- Several Non-Hodgkin's lymphomas, including Burkitt's lymphoma and primary cerebral lymphoma
- Post-transplant lymphoproliferative disorder
- Smooth muscle tumors[11]
- Stevens–Johnson syndrome
- Subepithelial Infiltrates
- New Daily Persistent Headache (NDPH)
See also
References
- ^ Bouvard, V; Baan, R; Straif, K; Grosse, Y; Secretan, B; El Ghissassi, F; Benbrahim-Tallaa, L; Guha, N; Freeman, C; Galichet, L; Cogliano, V; WHO International Agency for Research on Cancer Monograph Working Group (2009). "A review of human carcinogens--Part B: Biological agents". The lancet oncology 10 (4): 321–2. doi:10.1016/S1470-2045(09)70096-8. PMID 19350698.
- ^ Bennett, NJ (12 October 2008). "Mononucleosis and Epstein–Barr Virus Infection". eMedicine. Retrieved 2008-10-05.
- ^ Lerner, AM; Beqaj, SH; Deeter, RG; Fitzgerald, JT (2004). "IgM serum antibodies to Epstein–Barr virus are uniquely present in a subset of patients with the chronic fatigue syndrome". In Vivo 18 (2): 101–6. PMID 15113035.
- ^ Lünemann, Jan D.; Münz, Christian (2007). "Epstein–Barr virus and multiple sclerosis". Current Neurology and Neuroscience Reports 7 (3): 253–8. doi:10.1007/s11910-007-0038-y. PMID 17488592.
- ^ "Burkitt lymphoma". MedlinePlus. Retrieved 2012-04-10.
- ^ Weiss, Sharon W. (2002). "Smooth muscle tumors of soft tissue". Advances in Anatomic Pathology 9 (6): 351–9. doi:10.1097/00125480-200211000-00004. PMID 12409644.
- ^ "Nasopharyngeal Cancer". HealthCommunities.com. 7 December 2011.
- ^ Fleisher, G.; Bolognese, R. (1983). "Persistent Epstein–Barr virus infection and pregnancy". Journal of Infectious Diseases 147 (6): 982–6. doi:10.1093/infdis/147.6.982. PMID 6304207.
- ^ "Epstein–Barr Virus and Infectious Mononucleosis". National Center for Infectious Diseases. 16 May 2006. Retrieved 2008-10-05.
- ^ Tsai, JD; Lee, HC; Lin, CC; Liang, DC; Chen, SH; Huang, FY (2003). "Epstein–Barr virus-associated acute renal failure: diagnosis, treatment, and follow-up". Pediatric Nephrology 18 (7): 667–674. doi:10.1007/s00467-003-1152-y. PMID 12750978.
- ^ Deyrup, Andrea T; Lee, Victor K; Hill, Charles E; Cheuk, Wah; Toh, Han Chong; Kesavan, Sittampalam; Chan, Errol Wei??en; Weiss, Sharon W (2006). "Epstein–Barr virus-associated smooth muscle tumors are distinctive mesenchymal tumors reflecting multiple infection events: A clinicopathologic and molecular analysis of 29 tumors from 19 patients". American Journal of Surgical Pathology 30 (11): 75–82. doi:10.1097/01.pas.0000178088.69394.7b. PMID 16330945.
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