WordNet
- inflammation of the liver caused by a virus or a toxin
- the 5th letter of the Roman alphabet (同)e
- the base of the natural system of logarithms; approximately equal to 2.718282...
PrepTutorEJDIC
- 肝[臓]炎
- einsteiniumの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/05/03 00:39:49」(JST)
wiki en
| Hepatitis E | |
|---|---|
|
Hepatitis E virus
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| Classification and external resources | |
| ICD-10 | B17.2 |
| ICD-9 | 070.4 |
| DiseasesDB | 5794 |
| eMedicine | med/995 |
| MeSH | D016751 |
Hepatitis E is a viral hepatitis (liver inflammation) caused by infection with a virus called hepatitis E virus (HEV). It is one of five known human hepatitis viruses: A, B, C, D, and E. HEV is a positive-sense single-stranded RNA icosahedral virus with a 7.5 kilobase genome. HEV has a fecal-oral transmission route. Infection with this virus was first documented in 1955 during an outbreak in New Delhi, India.[1] A preventative vaccine (HEV 239) is approved for use in China.[2]
Although Hepatitis E often causes an acute and self-limiting infection (it usually goes away by itself and the patient recovers) with low mortality rates in the western world, it bears a high risk of developing chronic hepatitis in immunocompromised patients with substantial mortality rates. Organ transplant recipients who receive immunosuppressive medication to prevent rejection are thought to be the main population at risk for chronic hepatitis E.[3] Furthermore, in healthy individuals during the duration of the infection (usually several weeks), the disease severely impairs a person’s ability to work, care for family members, and obtain food. Hepatitis E occasionally develops into an acute, severe liver disease, and is fatal in about 2% of all cases. Clinically, it is comparable to hepatitis A, but in pregnant women the disease is more often severe and is associated with a clinical syndrome called fulminant liver failure. Pregnant women, especially those in the third trimester, suffer an elevated mortality rate from the disease of around 20%.[4]
Contents
- 1 Signs and symptoms
- 1.1 Acute infection
- 1.2 Chronic infection
- 2 Virology
- 2.1 Classification
- 2.2 Distribution
- 2.3 Transmission
- 2.4 Animal reservoir
- 2.5 Molecular biology
- 3 Prevention
- 3.1 Sanitation
- 3.2 Vaccines
- 4 Treatment
- 5 Epidemiology
- 5.1 Recent outbreaks
- 6 History
- 7 References
- 8 External links
Signs and symptoms
Acute infection
The incubation period of hepatitis E varies from 3 to 8 weeks. After a short prodromal phase symptoms lasting from days to weeks follow. They may include jaundice, fatigue and nausea. The symptomatic phase coincides with elevated hepatic aminotransferase levels.[5]
Viral RNA becomes detectable in stool and blood serum during incubation period. Serum IgM and IgG antibodies against HEV appear just before onset of clinical symptoms. Recovery leads to virus clearance from the blood, while the virus may persist in stool for much longer. Recovery is also marked by disappearance of IgM antibodies and increase of levels of IgG antibodies.[5]
Chronic infection
While usually an acute disease, in immunocompromised subjects—particularly in solid organ transplanted patients—hepatitis E may cause a chronic infection.[6] Occasionally this may cause liver fibrosis and cirrhosis.
Virology
Classification
There is only one serotype of the virus and classification is based on the nucleotide sequences of the genome.[7] Genotype 1 has been classified into five subtypes, genotype 2 into two subtypes and genotypes 3 and 4 have been into ten and seven subtypes respectively.
Differences have been noted between the different genotypes. For genotype 1, the age at which incidence peaks is between 15 and 35 years and mortality is about 1%. Genotype 3 and 4—the most common in Japan—are more common in people older than 60 years and the mortality is between 5 and 10%.[8]
Distribution
Genotype 1 has been isolated from tropical and several subtropical countries in Asia and Africa. Genotype 2 has been isolated from Mexico, Nigeria, and Chad. Genotype 3 has been isolated almost worldwide including Asia, Europe, Oceania, North and South America. Genotype 4 appears to be limited exclusively to Asia.
Genotypes 1 and 2 are restricted to humans and often associated with large outbreaks and epidemics in developing countries with poor sanitation conditions. Genotypes 3 and 4 infect humans, pigs and other animal species and have been responsible for sporadic cases of hepatitis E in both developing and industrialized countries.
In the United Kingdom the Department for Environment, Food and Rural Affairs (DEFRA) said that the number of human hepatitis E cases increased by 39% between 2011 and 2012.[9]
Transmission
Hepatitis E is prevalent in most developing countries, and common in any country with a hot climate. It is widespread in Southeast Asia, northern and central Africa, India, and Central America. It is spread mainly by the fecal-oral route due to fecal contamination of water supplies or food; person-to-person transmission is uncommon.
The incubation period following exposure to the hepatitis E virus ranges from three to eight weeks, with a mean of 40 days.[10] Outbreaks of epidemic hepatitis E most commonly occur after heavy rainfalls and monsoons because of their disruption of water supplies. Major outbreaks have occurred in New Delhi, India (30,000 cases in 1955–1956), Burma (20,000 cases in 1976–1977), Kashmir, India (52,000 cases in 1978), Kanpur, India (79,000 cases in 1991), and China (100,000 cases between 1986 and 1988).
DEFRA said that there was evidence that the increase in hepatitis E in the UK was due to food-borne zoonoses, citing a study that found 10% of pork sausages on sale in the UK contained the virus. Some research suggests that food must reach a temperature of 70°C for 20 minutes to eliminate the risk of infection. An investigation by the Animal Health and Veterinary Laboratories Agency found hepatitis E in 49% of pigs in Scotland.[9]
Animal reservoir
Domestic animals have been reported as a reservoir for the hepatitis E virus, with some surveys showing infection rates exceeding 95% among domestic pigs.[11] Replicative virus has been found in the small intestine, lymph nodes, colon and liver of experimentally infected pigs. Transmission after consumption of wild boar meat and uncooked deer meat has been reported as well.[12] The rate of transmission to humans by this route and the public health importance of this are, however, still unclear.[13]
A number of other small mammals have been identified as potential reservoirs: the lesser bandicoot rat (Bandicota bengalensis), the black rat (Rattus rattus brunneusculus) and the Asian house shrew (Suncus murinus).[14] A new virus designated rat hepatitis E virus has been isolated.[15]
A rabbit hepatitis E virus has also been described,[16] with a study published in 2014 showing that research rabbits from two different American vendors showed seroprevalences of 40% for Supplier A and 50% for Supplier B when testing for antibodies against hepatitis E virus (HEV). Supplier A was a conventional rabbit farm, and supplier B was a commercial vendor of specific pathogen free (SPF) research rabbits. The study remarks "HEV probably is widespread in research rabbits, but effects on research remain unknown." Laboratory animal care personnel, researchers, and support staff represent a new population at risk for HEV infection, and research facilities should be diligent in measures to prevention of this possibly zoonotic pathogen.[17]
An avian virus has been described that is associated with hepatitis-splenomegaly syndrome in chickens. This virus is genetically and antigenically related to mammalian HEV, and probably represents a new genus in the family.
Molecular biology
Although it was originally classified in the Caliciviridae family, the virus has since been classified into the genus Orthohepevirus, and has been reassigned into the Hepeviridae family. The virus itself is a small non-enveloped particle.
The genome is approximately 7200 bases in length, is a polyadenylated single-strand RNA molecule that contains three discontinuous and partially overlapping open reading frames (ORFs) along with 5' and 3' cis-acting elements, which have important roles in HEV replication and transcription. ORF1 encode a methyltransferase, protease, helicase and replicase; ORF2 encode the capsid protein and ORF3 encodes a protein of undefined function. A three-dimensional, atomic-resolution structure of the capsid protein in the context of a virus-like particle has been described.[18] An in vitro culture system is not yet available.
As of 2009 there are approximately 1,600 sequences of both human and animal isolates of HEV available in open-access sequence databases.
Species of this genus infect humans, pigs, boars, deer, rats, rabbits and birds.[19]
Prevention
Sanitation
Improving sanitation is the most important measure in prevention of hepatitis E; this consists of proper treatment and disposal of human waste, higher standards for public water supplies, improved personal hygiene procedures and sanitary food preparation. Thus, prevention strategies of this disease are similar to those of many others that plague developing nations, and they require large-scale international financing of water supply and water treatment projects.
Vaccines
A vaccine based on recombinant viral proteins was developed in the 1990s and tested in a high-risk population (military personnel of Nepal) in 2001.[20] The vaccine appeared to be effective and safe, but development was stopped for economic reasons, since hepatitis E is rare in developed countries.[2] There is no licensed hepatitis E vaccine for use in the US.
Although other HEV vaccine trials, including trials conducted in populations in southern Asia, have shown candidate vaccines to be effective and well-tolerated, these vaccines have not yet been produced or made available to susceptible populations. The exception is China. After more than a year of scrutiny and inspection by China's State Food and Drug Administration (SFDA), a hepatitis E vaccine developed by Chinese scientists was available at the end of 2012. This vaccine—called HEV 239 and sold as Hecolin by its developer Xiamen Innovax Biotech—was approved for prevention of hepatitis E in 2012 by the Chinese Ministry of Science and Technology, following a phase 3 trial on two groups of 50,000 people each from Jiangsu Province where none of the vaccinated became infected during a 12-month period, compared to 15 in the group given placebo treatment.[21] The first vaccine batches came out of Innovax' factory in late October 2012, and will be sold to Chinese distributors.[2]
Treatment
Apart from supportive care, no specific validated treatment exists for acute hepatis E infection. Although ribavirin is not registered for Hepatitis E treatment, there is off-label experience for treating chronic Hepatitis E with this compound. The use of low doses, 600 to 800 milligrams per day, of ribavirin over a three-month period has been associated with viral clearance in about two-thirds of chronic cases.[3] Other possible treatments include peginterferon or a combination of ribavirin and peginterferon. In general chronic HEV infection is associated with immunosuppressive therapies, but remarkably little is known about how different immunosuppressants affect HEV infection. In one thirds of patients with solid-organ transplantation viral clearance can be achieved by temporal reduction of the level of immunosuppression.[5]
Epidemiology
The hepatitis E virus causes around 20 million infections a year. These result in around three million acute illnesses and as of 2010, 57,000 deaths annually.[22] It is particularly dangerous for pregnant women, who can develop an acute form of the disease that is lethal in 20 percent of cases. The virus (HEV) is a major cause of illness and of death in the developing world and disproportionate cause of deaths among pregnant women. Among indigenous people, a significant prevalence of hepatitis E virus-specific antibody has been reported in several amerindian Yupka tribes in South America.[23]
Recent outbreaks
In 2004, there were two major outbreaks, both of them in sub-Saharan Africa. There was an outbreak in Chad in which, as of September 27, there were 1,442 reported cases and 46 deaths. The second was in Sudan with, as of September 28, 6,861 cases and 87 deaths. Increasingly, hepatitis E is being seen in developed nations, with reports of cases in the UK, US and Japan. The disease is thought to be a zoonosis in that animals are thought to be the source. Both deer and swine have been implicated.
In October 2007, an epidemic of hepatitis E was suspected in Kitgum District of northern Uganda where no previous epidemics had been documented. This outbreak has progressed to become one of the largest hepatitis E outbreaks in the world. By June 2009, the epidemic had caused illness in >10,196 persons and 160 deaths.[24]
In 2011, a minor outbreak was reported in Tangail, a neighborhood of Dhaka, Bangladesh.[25]
In June 2012, an outbreak was reported in city of Ichalkaranji, Maharashtra, India. As of June 14, 2012, 3232 cases were reported and 18 died.[26] and 3 died in Shirol taluka of Kolhapur Maharashtra, India in June 2012. Officials in the Indian state of Maharashtra India suspect that contaminated water from the Panchganga river was responsible for the hepatitis E outbreak in Ichalkaranji.
In July 2012, an outbreak was reported in South Sudanese refugee camps in Maban County near the Sudan border. South Sudan's Ministry of Health reported over 400 cases and 16 fatalities as of September 13, 2012.[27] Progressing further, as of February 2, 2013, 88 have died due to the outbreak. The "Medical charity Medecins Sans Frontieres (MSF) said it had treated almost 4,000 patients."[28]
In April 2014 there was an outbreak in Nepal, Biratnagar Municipality with over 6,000 locals infected and at least 9 dead.[29]
History
The most recent common ancestor of Hepatitis E evolved between 536 and 1344 years ago.[19] It diverged into two clades—an anthropotropic and an enzootic form—which subsequently evolved into genotypes 1 and 2 and genotypes 3 and 4 respectively. The divergence dates for the various genotypes are as follows: Genotypes 1/2 367–656 years ago; Genotypes 3/4 417–679 years ago. For the most recent common ancestor of the various viruses themselves: Genotype 1 between 87 and 199 years ago; Genotype 3 between 265 and 342 years ago; and Genotype 4 between 131 and 266 years ago. The anthropotropic strains (genotype 1 and 2) have evolved more recently than the others suggesting that this virus was originally a zooenosis.
The use of an avian strain confirmed the proposed topology of the genotypes 1–4 and suggested that the genus may have evolved 1.36 million years ago (range 0.23 million years ago to 2.6 million years ago).[19] The use of a rat sequence also confirmed this topology and estimated date of divergence from the swine/human strains was 7.44×104 years ago (range 2.1×104 to 1.4×105 years ago). Since this date is approximately coincident with the advent of agriculture it may be that this virus originally infected rats and subsequently spread to pigs and then to humans. Additional work is required to support or refute this possibility as very few sequences have been isolated from species other than humans and suids.[30]
Genotypes 1, 3 and 4 all increased their effective population sizes in the 20th century.[19] The population size of genotype 1 increased noticeably in the last 30–35 years. Genotypes 3 and 4 population sizes began to increase in the late 19th century up to 1940–1945. Genotype 3 underwent a subsequent increase in population size until the 1960s. Since 1990 both genotypes' population sizes have been reduced back to levels last seen in the 19th century.
The overall mutation rate for the genome has been estimated at ~1.4×10−3 substitutions/site/year.[19]
References
This article incorporates public domain text from the CDC as cited
- ^ Gupta DN, Smetana HF; Smetana (1957). "The histopathology of viral hepatitis as seen in the Delhi epidemic (1955–56)". Indian J. Med. Res. 45 (Suppl): 101–13. PMID 13438544.
- ^ a b c Park, S. B. (November 2012). "Hepatitis E vaccine debuts". Nature 491 (7422): 21–22. doi:10.1038/491021a. PMID 23128204. edit
- ^ a b Zhou X, de Man RA, de Knegt RJ, Metselaar HJ, Peppelenbosch MP, Pan Q.; De Man; De Knegt; Metselaar; Peppelenbosch; Pan (2013). "Epidemiology and management of chronic hepatitis E infection in solid organ transplantation: a comprehensive literature review". Rev Med Virol. 23 (5): 295–304. doi:10.1002/rmv.1751. PMID 23813631.
- ^ WHO. "Global Alert and Response (GAR); Hepatitis E". Retrieved 26 January 2012.
- ^ a b c Hoofnagle, J. H.; Nelson, K. E.; Purcell, R. H. (2012). "Hepatitis E". New England Journal of Medicine 367 (13): 1237–1244. doi:10.1056/NEJMra1204512. PMID 23013075. edit
- ^ Bonnet, D.; Kamar, N.; Izopet, J.; Alric, L. (2012). "L'hépatite virale E : Une maladie émergente". La Revue de Médecine Interne 33 (6): 328–334. doi:10.1016/j.revmed.2012.01.017. PMID 22405325. edit
- ^ Lu L, Li C, Hagedorn CH; Li; Hagedorn (2006). "Phylogenetic analysis of global hepatitis E virus sequences: genetic diversity, subtypes and zoonosis". Rev Med Virol 16 (1): 5–36. doi:10.1002/rmv.482. PMID 16175650.
- ^ Miyahara K, Miyake Y, Yasunaka T et al. (2010). "Acute hepatitis due to hepatitis E virus genotype 1 as an imported infectious disease in Japan". Intern. Med. 49 (23): 2613–6. doi:10.2169/internalmedicine.49.4221. PMID 21139302.
- ^ a b Doward, Jamie (21 September 2013). "Chefs fight for the right to serve their pork pink". The Observer newspaper. Retrieved 22 September 2013.
- ^ "Hepatitis E Fact sheet".
- ^ Satou K, Nishiura H; Nishiura (2007). "Transmission Dynamics of Hepatitis E Among Swine: Potential Impact upon Human Infection". BMC Vet. Res. 3: 9. doi:10.1186/1746-6148-3-9. PMC 1885244. PMID 17493260.
- ^ Li TC, Chijiwa K, Sera N et al. (2005). "Hepatitis E Virus Transmission from Wild Boar Meat". Emerging Infect. Dis. 11 (12): 1958–60. doi:10.3201/eid1112.051041. PMC 3367655. PMID 16485490.
- ^ Kuniholm MH & Nelson KE (2008). "Of Organ Meats and Hepatitis E Virus: One Part of a Larger Puzzle Is Solved". J Infect Dis 198 (12): 1727–1728. doi:10.1086/593212. PMID 18983247.
- ^ "Wild Rats and Disease".
- ^ Johne R, Plenge-Bönig A, Hess M, Ulrich RG, Reetz J, Schielke A; Plenge-Bönig; Hess; Ulrich; Reetz; Schielke (March 2010). "Detection of a novel hepatitis E-like virus in faeces of wild rats using a nested broad-spectrum RT-PCR". J. Gen. Virol. 91 (Pt 3): 750–8. doi:10.1099/vir.0.016584-0. PMID 19889929.
- ^ Cheng X, Wang S, Dai X, Shi C, Wen Y, Zhu M, Zhan S, Meng J; Wang; Dai; Shi; Wen; Zhu; Zhan; Meng (2012). "Rabbit as a novel animal model for hepatitis e virus infection and vaccine evaluation". PLoS ONE 7 (12): e51616. doi:10.1371/journal.pone.0051616. PMC 3521758. PMID 23272124.
- ^ Birke L, Cormier SA, You D, Stout RW, Clement, Johnson M, et al. Hepatitis E antibodies in laboratory rabbits from 2 US vendors. Emerg Infect Dis [Internet]. 2014 Apr [April 3, 2014]. http://dx.doi.org/10.3201/eid2004.131229
- ^ Tao, TS; Liu, Z; Ye, Q; Mata, DA; Li, K; Yin, C; Zhang, J; Tao, YJ (Aug 4, 2009). "Structure of the hepatitis E virus-like particle suggests mechanisms for virus assembly and receptor binding". Proceedings of the National Academy of Sciences of the United States of America 106 (31): 12992–7. Bibcode:2009PNAS..10612992G. doi:10.1073/pnas.0904848106. PMC 2722310. PMID 19622744.
- ^ a b c d e Purdy MA, Khudyakov YE; Khudyakov (2010). Tavis, John E, ed. "Evolutionary history and population dynamics of hepatitis E virus". PLoS ONE 5 (12): e14376. doi:10.1371/journal.pone.0014376. PMC 3006657. PMID 21203540.
- ^ Shrestha MP, Scott RM, Joshi DM et al. (2007). "Safety and efficacy of a recombinant hepatitis E vaccine". N. Engl. J. Med. 356 (9): 895–903. doi:10.1056/NEJMoa061847. PMID 17329696.
- ^ Proffitt, A. (2012). "First HEV vaccine approved". Nature Biotechnology 30 (4): 300–301. doi:10.1038/nbt0412-300a. PMID 22491268. edit
- ^ Lozano, R; Naghavi, M; Foreman, K; Lim, S; Shibuya, K; Aboyans, V; Abraham, J; Adair, T; Aggarwal, R; Ahn, SY; Alvarado, M; Anderson, HR; Anderson, LM; Andrews, KG; Atkinson, C; Baddour, LM; Barker-Collo, S; Bartels, DH; Bell, ML; Benjamin, EJ; Bennett, D; Bhalla, K; Bikbov, B; Bin Abdulhak, A; Birbeck, G; Blyth, F; Bolliger, I; Boufous, S; Bucello, C et al. (Dec 15, 2012). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet 380 (9859): 2095–128. doi:10.1016/S0140-6736(12)61728-0. PMID 23245604.
- ^ Echevarría, JM; Blitz-Dorfman, L; Pujot, FH (September 1996). "[Infection by hepatitis virus among the indigenous populations of South America: a review of the problem].". Investigacion clinica 37 (3): 191–200. PMID 8983357. Retrieved Dec 14, 2014.
- ^ Teshale EH, Howard CM, Grytdal SP et al. (January 2010). "Hepatitis E epidemic, Uganda". Emerging Infect. Dis. 16 (1): 126–9. doi:10.3201/eid1601.090764. PMC 2874362. PMID 20031058.
- ^ Nurul Islam Hasib (June 14, 2011). "Hepatitis E sounds alarm". bdnews24.com. Retrieved June 20, 2012.
- ^ "18 killed in hepatitis E outbreak in Maharashtra". Daily News (New York). Retrieved June 20, 2012.
- ^ Hereward Holland (September 13, 2012). "Hepatitis outbreak kills 16 in South Sudan refugee camps". Retrieved September 15, 2012.
- ^ Hereward Holland (February 2, 2013). "Hepatitis outbreak kills 88 in South Sudan—aid agency". Reuters. Retrieved February 6, 2013.
- ^ "Nine killed, 6000 fall ill due to Hepatitis E in Morang". Republica. 8 May 2014. Retrieved 4 August 2014.
- ^ =https://en.wikipedia.org/wiki/Suidae
External links
- "Hepatitis E". Media centre: Fact sheet N°280. World Health Organization. July 2013.
- Virus Pathogen Database and Analysis Resource (ViPR): Hepeviridae
- Aggarwa, Rakesh; Gandhi, Sanjay (December 2010). "A systematic review on prevalence of hepatitis E disease and seroprevalence of hepatitis E virus antibody" (PDF). World Health Organization. WHO/IVB/10.14.
- Bjorn, Genevive (18 October 2010). "The night my liver started running my life". New York Times.
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UpToDate Contents
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- 1. E型肝炎ウイルス感染 hepatitis e virus infection
- 2. 中央アフリカへの旅行によって感染する可能性のある疾患 diseases potentially acquired by travel to central africa
- 3. 肝炎ウイルスと新生児：臨床症状および治療 hepatitis viruses and the newborn clinical manifestations and treatment
- 4. 南アジアへの旅行によって感染する可能性のある疾患 diseases potentially acquired by travel to south asia
- 5. 妊娠時の肝胆道系疾患併発 intercurrent hepatobiliary disease during pregnancy
English Journal
- The hepatitis E virus ORF1 'X-domain' residues form a putative macrodomain protein/Appr-1″-pase catalytic-site, critical for viral RNA replication.
- Parvez MK1.
- Gene.Gene.2015 Jul 15;566(1):47-53. doi: 10.1016/j.gene.2015.04.026. Epub 2015 Apr 11.
- The hepatitis E virus (HEV) ORF1 gene encodes the non-structural polyprotein wherein the 'X-domain' still remains poorly defined. Cellular X-domain associated macrodomain protein/ADP-ribose-1″-monophosphatase (Appr-1″-pase) activities are also reported in coronaviruses (CoV), including identific
- PMID 25870943
- Design and production of a multiepitope construct derived from hepatitis E virus capsid protein.
- Taherkhani R1, Farshadpour F, Makvandi M.
- Journal of medical virology.J Med Virol.2015 Jul;87(7):1225-34. doi: 10.1002/jmv.24171. Epub 2015 Mar 17.
- The aim of this study was to design a high density multiepitope protein, which can be a promising multiepitope vaccine candidate against Hepatitis E virus (HEV). Initially, conserved and antigenic helper T-lymphocyte (HTL) epitopes in the HEV capsid protein were predicted by in silico analysis. Subs
- PMID 25784455
- Full genome analysis of a European-type genotype 3 hepatitis E virus variant obtained from a Japanese patient with autochthonous acute hepatitis E.
- Takeuchi S1, Yamazaki Y, Sato K, Takizawa D, Yamada M, Okamoto H.
- Journal of medical virology.J Med Virol.2015 Jul;87(7):1067-71. doi: 10.1002/jmv.24191. Epub 2015 Mar 16.
- A unique European-type HEV strain (HE-JA12-0725) classifiable into subgenotype 3f was recovered from a 66-year-old Japanese female with autochthonous acute hepatitis E, and its entire genomic sequence was determined and characterized. The HE-JA12-0725 strain shared the highest identity of 92.7% with
- PMID 25777997
Japanese Journal
- Development of an Infectious Surrogate Hepatitis C Virus Based on a Recombinant Vesicular Stomatitis Virus Expressing Hepatitis C Virus Envelope Glycoproteins and Green Fluorescent Protein
- Okuma Kazu,Fukagawa Koji,Tateyama Seiji [他]
- Japanese Journal of Infectious Diseases 68(3), 203-208, 2015-05
- NAID 40020471291
- B型肝炎再活性化とがん化学療法 (特集 外科医が知っておくべきがん薬物療法の副作用とその対策)
- 赤星 径一,松村 聡,光法 雄介 [他]
- 臨床外科 = Journal of clinical surgery 70(5), 532-536, 2015-05
- NAID 40020445692
- Beneficial Effects of Camellia Oil (Camellia oleifera Abel.) on Hepatoprotective and Gastroprotective Activities (Nutrition and Food for Longevity : For the Well-Being of All : Proceedings of the 12th Asian Congress of Nutrition)
- CHENG Yu-Ting,LU Chi-Cheng,YEN Gow-Chin
- Journal of nutritional science and vitaminology 61(Suppl.), S100-102, 2015-05
- NAID 40020444296
Related Links
- Hepatitis E is a liver disease caused by the hepatitis E virus: a non-enveloped, positive-sense, single-stranded RNA virus. ... Hepatitis E is found worldwide and different genotypes of the hepatitis E virus determine differences in epidemiology.
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★リンクテーブル★
| リンク元 | 「E型肝炎」 |
| 関連記事 | 「Es」「E」 |
「E型肝炎」
- 英
- hepatitis E
- 関
- E型肝炎ウイルス
病原体
潜伏期
- 1-2ヶ月 (SMB.553)
感染経路
- 経口感染
- 汚染食物、飲料水を介する
疫学
症状
- 全身倦怠感、発熱、嘔吐、黄疸など慢性肝炎 (SMB.553)
- 1ヶ月で治癒
- 劇症肝炎に移行しうる
- 通常、1-2%, 妊婦の死亡率10-20%
合併症
経過
治療
検査
予防
「Es」
「E」