Leta i den här bloggen

fredag 20 maj 2022

MPXV eli Orthopox virus simiae- lajia on käytetty myös vektorin tavoin kutn adenovirusta rokotevalmistelun joissain vaiheissa.

 ESIMERKKI rokotevalmistelujen  vaiheista:

https://pubmed.ncbi.nlm.nih.gov/28792942/

 

HIV-1-neutralizing antibody induced by simian adenovirus- and poxvirus MVA-vectored BG505 native-like envelope trimers

Affiliations
Free PMC article

Abstract

Rabbits and monkeys immunized with HIV type 1 (HIV-1) native-like BG505 SOSIP.664 (BG505s) glycoprotein trimers are known to induce antibodies that can neutralize the autologous tier-2 virus. Here, we assessed the induction of HIV-1 trimer binding and neutralizing antibody (nAb) titres when BG505s trimers were also delivered by non-replicating simian (chimpanzee) adenovirus and non-replicating poxvirus modified vaccinia virus Ankara (MVA) vaccine vectors. First, we showed that approximately two-thirds and one-third of the trimers secreted from the ChAdOx1.BG505s (C) and MVA.BG505s (M) vaccine-infected cells, respectively, were cleaved and in a native-like conformation. Rabbits were immunized intramuscularly with these vaccine vectors and in some cases boosted with ISCOMATRIX™-adjuvanted BG505s protein trimer (P), using CCC, MMM, PPP, CPP, MPP and CMP vaccine regimens. We found that the peak trimer-binding antibody and tier-1A and autologous tier-2 nAb responses induced by the CC, CM, PPP, CPP, MPP and CMP regimens were comparable, although only PPP induced autologous tier-2 nAbs in all the immunized animals. Three animals developed weak heterologous tier-2 nAbs. These results demonstrate that ChAdOx1 and MVA vectors are useful delivery modalities for not only T-cell, but also antibody vaccine development.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

WHO mainitsee tapauksia monkeypox nimisestä ortopoxviruksesta, joka on sukua jo hävinneelle isorokkovirukselle

 Ne joilla  puoli vuosisataa sitten on ollut  voimassa oleva isorokkorokotus, mahdollisesti omaavat edelleen tätä pox-viruslajia vastaan ehkä 85% suojaa erään lähteen mukaan.  Satun itse  olemaan kahdesti rokotettu  isoarokkoa vastaan, 1967 ja 1972, Israelin matkojeni yhteydessä. Jälkimmäinn rokote tuli saatua Nasaretissa, koska siellä sairaalaväki rokotettiin  Syyriassa ilmenneen isorokkotapauksen takia.  Ensimmäisen kerran otin rokotuksen, koska se oli vaatimuksena  Israelin matkalle lähtöön.  Iisorokosta sinänsä ei ole kuulunut kai mitään niiten vuosikymmenien jälkeen, muta  virusta säilytetään jossain  varalta , ehkä mahdollisiin tulevisuuden rokotetarpeisiin. 

Nyt lehdistössä puhutaan  tuosta monkeypox-tyypistä, jota on ilmennyt ihmiskunnan puolella. Etsin WHO:n . kirjoituksen  tästä asiasta: 

Key facts

  • Monkeypox is caused by monkeypox virus, a member of the Orthopoxvirus genus in the family Poxviridae.
  • Monkeypox is a viral zoonotic disease that occurs primarily in tropical rainforest areas of Central and West Africa and is occasionally exported to other regions.
  • Monkeypox typically presents clinically with fever, rash and swollen lymph nodes and may lead to a range of medical complications.
  • Monkeypox is usually a self-limited disease with the symptoms lasting from 2 to 4 weeks. Severe cases can occur. In recent times, the case fatality ratio has been around 3-6%.
  • Monkeypox is transmitted to humans through close contact with an infected person or animal, or with material contaminated with the virus.
  • Monkeypox virus is transmitted from one person to another by close contact with lesions, body fluids, respiratory droplets and contaminated materials such as bedding.
  • The clinical presentation of monkeypox resembles that of smallpox, a related orthopoxvirus infection which was declared eradicated worldwide in 1980. Monkeypox is less contagious than smallpox and causes less severe illness.
  • Vaccines used during the smallpox eradication programme also provided protection against monkeypox. Newer vaccines have been developed of which one has been approved for prevention of monkeypox
  • An antiviral agent developed for the treatment of smallpox has also been licensed for the treatment of monkeypox.

 

Introduction

Monkeypox is a viral zoonosis (a virus transmitted to humans from animals) with symptoms very similar to those seen in the past in smallpox patients, although it is clinically less severe. With the eradication of smallpox in 1980 and subsequent cessation of smallpox vaccination, monkeypox has emerged as the most important orthopoxvirus for public health. Monkeypox primarily occurs in Central and West Africa, often in proximity to tropical rainforests and has been increasingly appearing in urban areas. Animal hosts include a range of rodents and non-human primates.

 

The pathogen

Monkeypox virus is an enveloped double-stranded DNA virus that belongs to the Orthopoxvirus genus of the Poxviridae family. There are two distinct genetic clades of the monkeypox virus – the Central African (Congo Basin) clade and the West African clade. The Congo Basin clade has historically caused more severe disease and was thought to be more transmissible. The geographical division between the two clades has so far been in Cameroon - the only country where both virus clades have been found.

 

Natural host of monkeypox virus

Various animal species have been identified as susceptible to monkeypox virus.. This includes rope squirrels, tree squirrels, Gambian pouched rats, dormice, non-human primates and other species. Uncertainty remains on the natural history of monkeypox virus and further studies are needed to identify the exact reservoir(s) and how virus circulation is maintained in nature.

 

Outbreaks

Human monkeypox was first identified in humans in 1970 in the Democratic Republic of the Congo in a 9-year-old boy in a region where smallpox had been eliminated in 1968. Since then, most cases have been reported from rural, rainforest regions of the Congo Basin, particularly in the Democratic Republic of the Congo and human cases have increasingly been reported from across Central and West Africa.

Since 1970, human cases of monkeypox have been reported in 11 African countries – Benin, Cameroon, the Central African Republic, the Democratic Republic of the Congo, Gabon, Cote d’Ivoire, Liberia, Nigeria, the Republic of the Congo, Sierra Leone, and South Sudan. The true burden of monkeypox is not known. For example, in 1996–97, an outbreak was reported in the Democratic Republic of the Congo with a lower case fatality ratio and a higher attack rate than usual. A concurrent outbreak of chickenpox (caused by the varicella virus, which is not an orthopoxvirus) and monkeypox was found which could explain real or apparent changes in transmission dynamics in this case. Since 2017, Nigeria has experienced a large outbreak, with over 500 suspected cases and over 200 confirmed cases and a case fatality ratio of approximately 3%. Cases continue to be reported until today.

Monkeypox is a disease of global public health importance as it not only affects countries in West and Central Africa, but the rest of the world. In 2003, the first monkeypox outbreak outside of Africa was in the United States of America and was linked to contact with infected pet prairie dogs. These pets had been housed with Gambian pouched rats and dormice that had been imported into the country from Ghana. This outbreak led to over 70 cases of monkeypox in the U.S. Monkeypox has also been reported in travelers from Nigeria to Israel in September 2018, to the United Kingdom in September 2018, December 2019, May 2021 and May 2022, to Singapore in May 2019, and to the United States of America in July and November 2021. In May 2022, multiple cases of monkeypox were identified in several non-endemic countries. Studies are currently underway to further understand the epidemiology, sources of infection, and transmission patterns.  


Transmission

Animal-to-human (zoonotic) transmission can occur from direct contact with the blood, bodily fluids, or cutaneous or mucosal lesions of infected animals. In Africa, evidence of monkeypox virus infection has been found in many animals including rope squirrels, tree squirrels, Gambian poached rats, dormice, different species of monkeys and others. The natural reservoir of monkeypox has not yet been identified, though rodents are the most likely. Eating inadequately cooked meat and other animal products of infected animals is a possible risk factor. People living in or near forested areas may have indirect or low-level exposure to infected animals.

Human-to-human transmission can result from close contact with respiratory secretions, skin lesions of an infected person or recently contaminated objects. Transmission via droplet respiratory particles usually requires prolonged face-to-face contact, which puts health workers, household members and other close contacts of active cases at greater risk. However, the longest documented chain of transmission in a community has risen in recent years from six to nine successive person-to-person infections. This may reflect declining immunity in all communities due to cessation of smallpox vaccination. Transmission can also occur via the placenta from mother to fetus (which can lead to congenital monkeypox) or during close contact during and after birth. While close physical contact is a well-known risk factor for transmission, it is unclear at this time if monkeypox can be transmitted specifically through sexual transmission routes. Studies are needed to better understand this risk.

Signs and symptoms

The incubation period (interval from infection to onset of symptoms) of monkeypox is usually from 6 to 13 days but can range from 5 to 21 days.

The infection can be divided into two periods:

  • the invasion period (lasts between 0-5 days) characterized by fever, intense headache, lymphadenopathy (swelling of the lymph nodes), back pain, myalgia (muscle aches) and intense asthenia (lack of energy). Lymphadenopathy is a distinctive feature of monkeypox compared to other diseases that may initially appear similar (chickenpox, measles, smallpox)
  • the skin eruption usually begins within 1-3 days of appearance of fever. The rash tends to be more concentrated on the face and extremities rather than on the trunk. It affects the face (in 95% of cases), and palms of the hands and soles of the feet (in 75% of cases). Also affected are oral mucous membranes (in 70% of cases), genitalia (30%), and conjunctivae (20%), as well as the cornea. The rash evolves sequentially from macules (lesions with a flat base) to papules (slightly raised firm lesions), vesicles (lesions filled with clear fluid), pustules (lesions filled with yellowish fluid), and crusts which dry up and fall off. The number of lesions varies from a few to several thousand. In severe cases, lesions can coalesce until large sections of skin slough off.

Monkeypox is usually a self-limited disease with the symptoms lasting from 2 to 4 weeks. Severe cases occur more commonly among children and are related to the extent of virus exposure, patient health status and nature of complications. Underlying immune deficiencies may lead to worse outcomes. Although vaccination against smallpox was protective in the past, today persons younger than 40 to 50 years of age (depending on the country) may be more susceptible to monkeypox due to cessation of smallpox vaccination campaigns globally after eradication of the disease.  Complications of monkeypox can include secondary infections, bronchopneumonia, sepsis, encephalitis, and infection of the cornea with ensuing loss of vision. The extent to which asymptomatic infection may occur is unknown.

The case fatality ratio of monkeypox has historically ranged from 0 to 11 % in the general population and has been higher among young children. In recent times, the case fatality ratio has been around 3-6%.

 

Diagnosis

The clinical differential diagnosis that must be considered includes other rash illnesses, such as chickenpox, measles, bacterial skin infections, scabies, syphilis, and medication-associated allergies. Lymphadenopathy during the prodromal stage of illness can be a clinical feature to distinguish monkeypox from chickenpox or smallpox.

If monkeypox is suspected, health workers should collect an appropriate sample and have it transported safely to a laboratory with appropriate capability. Confirmation of monkeypox depends on the type and quality of the specimen and the type of laboratory test. Thus, specimens should be packaged and shipped in accordance with national and international requirements. Polymerase chain reaction (PCR) is the preferred laboratory test given its accuracy and sensitivity. For this, optimal diagnostic samples for monkeypox are from skin lesions – the roof or fluid from vesicles and pustules, and dry crusts. Where feasible, biopsy is an option. Lesion samples must be stored in a dry, sterile tube (no viral transport media) and kept cold. PCR blood tests are usually inconclusive because of the short duration of viremia relative to the timing of specimen collection after symptoms begin and should not be routinely collected from patients.

As orthopoxviruses are serologically cross-reactive, antigen and antibody detection methods do not provide monkeypox-specific confirmation. Serology and antigen detection methods are therefore not recommended for diagnosis or case investigation where resources are limited. Additionally, recent or remote vaccination with a vaccinia-based vaccine (e.g. anyone vaccinated before smallpox eradication, or more recently vaccinated due to higher risk such as orthopoxvirus laboratory personnel) might lead to false positive results.

In order to interpret test results, it is critical that patient information be provided with the specimens including: a) date of onset of fever, b) date of onset of rash, c) date of specimen collection, d) current status of the individual (stage of rash), and e) age.

 

Therapeutics

Clinical care for monkeypox should be fully optimized to alleviate symptoms, manage complications and prevent long-term sequelae. Patients should be offered fluids and food to maintain adequate nutritional status. Secondary bacterial infections should be treated as indicated.  An antiviral agent known as tecovirimat that was developed for smallpox was licensed by the European Medical Association (EMA) for monkeypox in 2022 based on data in animal and human studies. It is not yet widely available.

If used for patient care, tecovirimat should ideally be monitored in a clinical research context with prospective data collection.

 

Vaccination

Vaccination against smallpox was demonstrated through several observational studies to be about 85% effective in preventing monkeypox. Thus, prior smallpox vaccination may result in milder illness. Evidence of prior vaccination against smallpox can usually be found as a scar on the upper arm. At the present time, the original (first-generation) smallpox vaccines are no longer available to the general public. Some laboratory personnel or health workers may have received a more recent smallpox vaccine to protect them in the event of exposure to orthopoxviruses in the workplace. A still newer vaccine based on a modified attenuated vaccinia virus (Ankara strain) was approved for the prevention of monkeypox in 2019. This is a two-dose vaccine for which availability remains limited. Smallpox and monkeypox vaccines are developed in formulations based on the vaccinia virus due to cross-protection afforded for the immune response to orthopoxviruses.

Prevention

Raising awareness of risk factors and educating people about the measures they can take to reduce exposure to the virus is the main prevention strategy for monkeypox. Scientific studies are now underway to assess the feasibility and appropriateness of vaccination for the prevention and control of monkeypox. Some countries have, or are developing, policies to offer vaccine to persons who may be at risk such as laboratory personnel, rapid response teams and health workers.

 

Reducing the risk of human-to-human transmission

Surveillance and rapid identification of new cases is critical for outbreak containment. During human monkeypox outbreaks, close contact with infected persons is the most significant risk factor for monkeypox virus infection. Health workers and household members are at a greater risk of infection. Health workers caring for patients with suspected or confirmed monkeypox virus infection, or handling specimens from them, should implement standard infection control precautions. If possible, persons previously vaccinated against smallpox should be selected to care for the patient.

Samples taken from people and animals with suspected monkeypox virus infection should be handled by trained staff working in suitably equipped laboratories. Patient specimens must be safely prepared for transport with triple packaging in accordance with WHO guidance for transport of infectious substances.

The identification in May 2022 of clusters of monkeypox cases in several non-endemic countries with no direct travel links to an endemic area is atypical. Further investigations  are underway to determine the likely source of infection and limit further onward spread. As the source of this outbreak is being investigated, it is important to look at all possible modes of transmission in order to safeguard public health. Further information on this outbreak can be found here

 

Reducing the risk of zoonotic transmission

Over time, most human infections have resulted from a primary, animal-to-human transmission. Unprotected contact with wild animals, especially those that are sick or dead, including their meat, blood and other parts must be avoided. Additionally, all foods containing animal meat or parts must be thoroughly cooked before eating.

 

Preventing monkeypox through restrictions on animal trade

Some countries have put in place regulations restricting importation of rodents and non-human primates. Captive animals that are potentially infected with monkeypox should be isolated from other animals and placed into immediate quarantine. Any animals that might have come into contact with an infected animal should be quarantined, handled with standard precautions and observed for monkeypox symptoms for 30 days.

 

How monkeypox relates to smallpox

The clinical presentation of monkeypox resembles that of smallpox, a related orthopoxvirus infection which has been eradicated. Smallpox was more easily transmitted and more often fatal as about 30% of patients died. The last case of naturally acquired smallpox occurred in 1977, and in 1980 smallpox was declared to have been eradicated worldwide after a global campaign of vaccination and containment. It has been 40 or more years since all countries ceased routine smallpox vaccination with vaccinia-based vaccines. As vaccination also protected against monkeypox in West and Central Africa, unvaccinated populations are now also more susceptible to monkeypox virus infection.

Whereas smallpox no longer occurs naturally, the global health sector remains vigilant in the event it could reappear through natural mechanisms, laboratory accident or deliberate release. To ensure global preparedness in the event of reemergence of smallpox, newer vaccines, diagnostics and antiviral agents are being developed. These may also now prove useful for prevention and control of monkeypox.

 

WHO response

WHO supports Member States with surveillance, preparedness and outbreak response activities for monkeypox in affected countries.  More information can be found here

 https://www.who.int/news/item/20-05-2022-who-working-closely-with-countries-responding-to-monkeypox

 




Isot dsDNA-virukset, POXviridae, Chordopoxviridae, Genus ORTHOPOX, Species ja muita POX-virussukuja

 dsDNA virus group

 Family POXVIRIDAE , Subfamily CHORDOPOXVIRIDAE 

Genus  ORTHOPOX

Vaccinia virus, (VAXV) *
 Camelpox virus ,(CMLV) *
Cowpox virus (CPXV)
Monkeypoxvirus, (MPXV),  Orthopoxvirus simiae *
Ectromelia virus ,(ECTV) *
Buffalopoxvirus
Elefantpoxvirus
Raccoonpox virus 
Skunkpox virus 
Taterapox virus 
Variola virus , (VARV)
Volepox virus , 
(Zoonotic viruses*

https://viralzone.expasy.org/149?outline=all_by_species

Genus  PARAPOX
Orf virus 

Genus AVIPOXVIRUS
Fowlpoxvirus

Genus CAPRIPOXVIRUS
Sheeppoxvirus 

Genus LEPORIPOXVIRUS
Myxomavirus 

Genus SUIPOXVIRUS 
Swinepoxvirus 

Genus MOLLUSCIPOXVIRUS
Molluscum  contagiosum virus  

 Genus  YATAPOXVIRUS 
Yaba Monkey tumorvirus

 Family POXVIRIDAE, Subfamily ENTOMOPOXVIRINAE

Genus ENTOMOPOXVIRUS A, (MMEV)

Genus ENTOMOPOXVIRUS B, (AMEV)

Genus ENTOMOPOXVIRUS C,  (CLEV) 


(POX viruksia on paljon lisää:
Esim  matelijoilla:
 subfamily CHORDOPOXVIRINAE
CROCODYLIDPOXVIRUS 
Crocodilepoxvirus 
Ihmisille tärkeitä ovat  zoonoottiset  POX-virukset.
 Isorokko on juurrettu pois maailmasta rokotuksin) .

Punkkivälitteisiltä taudeilta suojautuminen on punkin puremalta suojautumista

 Suomessa on  tämän päivän uutisten mukaan  runsaammin punkkikantaa liikkeellä verrattuna edellisvuosiín.Samalla kun ilmasto loämpiää, punkkien esiintymisvyöhyke kipuaa merrenpinnantasosta ja saaristokorkeuksista ihan sisämaakorkeuksiin . Jopa Lapissa on tavattu jotain punkkisorttia.  Aluksihan  punkkia oli lähinnä merenrantakylissä ja meren saaristossa.  Siten alkoi olla uutisia niistä Taiga-punkeista joita tuli idästä päin ja nyt on yleisvaroitusta: Itse asiassa ei ole varmaa aluetta , missä punkkia ei  voisi Suomessa olla, vaikka  monin paikoin se ei ole  ollut kovin yleinen asia. Otan sitaatin  IS-.lehdestä kokonaisuudessan. Ohjeet  ovat hyvät ja liitteennä oleva  videopätkä   on selventävä.

Punkit ovat aktivoituneet ”ihan täysillä” – toimi heti näin, jos punkki puree

Puutiaisia on paljon, ja niitä vastaan kannattaa suojautua, sanoo professori.

Valitettavasti selaimesi ei tue HTML5-videoita.
14:15

Puutiaiset eli punkit ovat aktivoituneet.

– Kauden aloitus tuli vähän myöhempään, kun kevät oli niin kylmä ja talvi jatkui jopa etelässä pitkään, professori Ilari Sääksjärvi Turun yliopiston biodiversiteettiyksiköstä kertoo.

Nyt kun päivälämpötilat alkavat olla korkeita, punkit ovat aktivoituneet suuressa osassa maata.

– Kannattaa olla taas varovainen. Punkkiliveen on parin viime viikon aikana on tullut ihmisiltä todella paljon havaintoja, mikä kertoo siitä, että kyllä puutiaiset ihan täysillä taas liikkeellä ovat.

Punkkilive on kansalaistiedehanke, johon tutkijat toivovat havaintoja puutiaisen levinneisyyden kartoitusta varten.

Viimeksi kuluneen kuukauden aikana Punkkiliveen on raportoitu jo reilut 9 000 punkkihavaintoa.

Runsaimmin havaintoja on tehty Etelä- ja Varsinais-Suomessa, mutta muutamia myös Lapissa, esimerkiksi Rovaniemellä.

Sääksjärvi luonnehtii havaintojen määrää tavanomaiseksi. Iso trendi on, että puutiaiset levittäytyvät voimakkaasti ja kiipeävät Suomessa koko ajan pohjoisemmaksi.

– Puutiaiskannat myös runsastuvat voimakkaasti. Yksi tekijä, joka tähän vaikuttaa, on ilmastonmuutos: lämpötilanmuutos tekee koko ajan olosuhteita puutiaisille paremmiksi.

Minkälainen punkkikesä on luvassa?

Alkavasta kesästä Sääksjärvi ennakoi viime kesien kaltaista, mikä tarkoittaa runsaita punkkihavaintoja.

– Sanoisin tavanomaiseksi. Mutta nythän ihmiset ovat jo tottuneet siihen, että puutiaisia on paljon ja niitä vastaan kannattaa suojautua.

Puutiaiskannat runsastuvat voimakkaasti.

Sääksjärvi sanoo, että suojautuminen on helppoa, joten punkkien takia luonnossa liikkumista ei kannata jättää.

– Puutiaisia on, mutta kyllä niiden kanssa toimeen tulee. Tärkeä ohje on, että kannattaa aina muistaa tehdä koko perheelle punkkitarkastus, kun liikkuu luonnossa tai käy vaikka piknikillä puistossa. Punkkisyyni on ilmainen suojakeino, eikä se vie kuin muutaman minuutin.

Jos liikkuu alueilla, joilla on puutiaisaivokuumetta, myös TBE-rokote on suojakeino.

– Borrelioosilta rokote ei kuitenkaan suojaa, joten punkkisyyni on siksi aina todella tärkeä.

Lue lisää: Puutiaisaivotulehduksen tapausmäärät kasvoivat selvästi viime vuonna – kansallinen rokotusohjelma laajenee

Poista punkki mahdollisimman nopeasti

Borrelioosia ja puutiaisaivokuumetta ihmiseen tartuttaa vain pieni osa punkeista, mutta mahdollisen tartunnan välttämiseksi kannattaa toimia nopeasti.

Borrelia-bakteerit elävät punkin suolessa, ja siksi usein kestää jopa vuorokauden ennen kuin ne siirtyvät puremakohdasta ihmiseen.

Puutiaisaivokuumetta aiheuttava virus tarttuu kuitenkin huomattavasti lyhyemmässä ajassa, sillä tämä virus elää punkin sylkirauhasissa ja siirtyy pureman alkaessa nopeasti ihmiseen.

Jotta välttäisi molemmat taudit, punkki pitää poistaa mahdollisimman pian. Mitä kauemmin punkki on iholla, sitä suuremmaksi tartunnan todennäköisyys kasvaa.

Jos näet iholla punkin, toimi heti näin

■ Ihoon pureutunut punkki poistetaan kapeakärkisillä pinseteillä tai punkkipihdeillä.

■ Jos poistovälinettä ei ole saatavilla, punkin voi poistaa sormillakin. Punkkia käsiteltäessä kannattaa käyttää suojahansikkaita tartuntojen ehkäisemiseksi.

■ Ota punkista kiinni mahdollisimman läheltä ihoa ja irrota se pyörittämällä ja vetämällä ylöspäin tasaisella voimalla.

■ Vältä ravistelemista tai repimistä, ettei punkin imukärsä irtoa ja jää ihoon. Ihoon mahdollisesti jääneet punkinosat poistuvat yleensä itsestään haavaeritteen mukana.

■ Puhdista lopuksi purema-alue huolellisesti, ja voit myös desinfioida ihon.

■ Hävitä poistettu punkki esimerkiksi polttamalla ja pese kädet huolellisesti saippualla ja vedellä punkin käsittelemisen jälkeen.

■ Terveydenhuollon ammattilaiseen on syytä olla yhteydessä, jos​ muutaman viikon kuluessa puremakohtaan ilmaantuu suurehko (yli 5 cm), rengasmainen, punoittava ihottuma-alue, jonka keskellä voi olla vaaleampaa ihoa.

■ Samoin on toimittava siinä tapauksessa, jos viikkoja punkinpureman jälkeen ilmaantuu epäselvää kuumeilua, niveloireita, lihasheikkoutta, pahoinvointia tai halvausoireita.

■ Ota yhteyttä terveydenhuollon ammattilaiseen myös silloin, jos punkin pureman saanut on raskaana.

Lähde: Terveyskylä

 



Omicron varianttia BA.4 koskevaa lähdeartikkelia . BA.4 linjalla on kykyä kasvaa BA.2 linjan kustannuksella.

 Tarkistin, miten BA.4 menestyy maailmanmatkallaan ja näyttääpä se menestyvän. Nyt siitä on mainittuna 1333 sekvenssiä  Ne jakantuvat eri maihin seuraavasti:

EteläAfrikassa  820  (2%) , (Muut ovat prosentulaaisti  0%),  USA:ssa 119, UK:ssa 91,  Itävallassa 80,  Tanskassa 43, Belgiassa 34, Saksassa 33,  Italiassa 24,Israelissa 24,  Australiassa 19, Hollannissa 11,  Espanjassa 10,Ranskassa 7, Kanadassa 7  Singaporessa 3, Sveitsissä 3,  Irlannissa 2 sekvenssiä , Chilessä 1, Uudessa Seelannissa 1. Botswanassa 1 sekvenssi.

BA.4 Publications & Resources

5 results
Publication
Publication
Continued Emergence and Evolution of Omicron in South Africa: New BA.4 and BA.5 lineages Houriiyah Tegally et al.medRxiv 2 May 2022.Sa uth Africas fourth COVID-19 wave was driven predominantly by three lineages (BA.1, BA.2 and BA.3) of the SARS-CoV-2 Omicron variant of concern. We have now identified two new lineages, BA.4 and BA.5. The spike proteins of BA.4 and BA.5 are identical, and comparable to BA.2 except for the addition of 69-70del, L452R, F486V and the wild type amino acid at Q493. The 69-70 deletion in spike allows these lineages to be identified by the proxy marker of S-gene target failure with the TaqPath COVID-19 qPCR assay. BA.4 and BA.5 have rapidly replaced BA.2, reaching more than 50% of sequenced cases in South Africa from the first week of April 2022 onwards. Using a multinomial logistic regression model, we estimate growth advantages for BA.4 and BA.5 of 0.08 (95% CI: 0.07 - 0.09) and 0.12 (95% CI: 0.09 - 0.15) per day respectively over BA.2 in South Africa.

onsdag 18 maj 2022

Pohjois-Korean 26-miljoonainen rokottamaton kansa potee nyt ensimmäistä varsinaista pandemia-aaltoa.

 Japanin Uutisista sitaatti:

world

 SITAATTI talteen 18.5. 2022 ruotsin aikaa 22:55.  P-Korea ei taida olla WHO:n jäsen. Mitenkähän sieltä saisi  valltisevan virussekvenssin analyysiin? Todennäköisesti kyse on jostain  omikronviruslinjasta, joissa on kyllä virulenttia  valinnanvaraa valmiina, ettei tarvitse olla edes mikään uusi linja kyseessä.  Toivotaan ,että N-Korea ottaa vastaan tarjottua apua ja että pyytaä myös itse  apua muilta kansoilta ja WHO:lta tässä vaiheessa, koska  on olemassa olevia  resursseja auttaa.  On jo tablettimuotoistakin  anti-Covid-lääkettä, jolla on tehoa  infektion 5 alkupäivän  ajanjaksolla saatuna antiviraalina.  Teestauskapasiteetit  ovat siellä tilanteeseen nähden  aivan riittämättömiä, joten  purkauksen todelliset luvut voivat olla paljon suuremmat. 

N Korea reports 232,880 suspected COVID-19 cases

9 Comments
By KIM TONG-HYUNG

North Korea on Wednesday reported 232,880 new cases of fever and another six deaths as leader Kim Jong Un accused officials of “immaturity” and “slackness” in handling the escalating COVID-19 outbreak ravaging across the unvaccinated nation.

The country’s anti-virus headquarters said 62 people have died and more than 1.7 million have fallen ill amid a rapid spread of fever since late April. It said more than a million people recovered but at least 691,170 remain in quarantine.

Outside experts say most of the illnesses would be COVID-19, although North Korea has been able to confirm only a small number of COVID-19 cases since acknowledging an omicron outbreak last week, likely because of insufficient testing capabilities.

A failure to control the outbreak could have dire consequences in North Korea, considering its broken health care system and its rejection of internationally offered vaccines that has left a population of 26 million unimmunized.

The outbreak is almost certainly greater than the fever tally, considering the lack of tests and resources to monitor the sick, and there’s also suspicion that North Korea is underreporting deaths to soften the blow for Kim, who already was navigating the toughest moment of his decade in power. The pandemic has further damaged an economy already broken by mismanagement and U.S.-led sanctions over Kim’s nuclear weapons and missiles development.

The North’s official Korean Central News Agency said Kim during a ruling party Politburo meeting on Tuesday criticized officials over their early pandemic response, which he said underscored “immaturity in the state capacity for coping with the crisis” and blamed the vulnerability on their “non-positive attitude, slackness and non-activity.”

He urged officials to strengthen virus controls at workplaces and make “redoubled efforts” to improve the supply of daily necessities and stabilize living conditions, the KCNA said Wednesday.

Kim’s comments came days after he ripped officials over how they were handling the distribution of medicine released from state reserves and mobilized his army to help transport the supplies to pharmacies in capital Pyongyang, which were made open 24 hours to deal with the crisis.

Before acknowledging COVID-19 infections last Thursday, North Korea had insisted of a perfect record in keeping out the virus that has reached nearly ever corner of the world, a claim that was widely doubted. But its extremely strict border closure, large-scale quarantines and propaganda that stressed anti-virus controls as a matter of “national existence” may have staved off a huge outbreak until now.

It’s unclear whether the North’s admission of a COVID-19 outbreak communicates a willingness to accept outside help. Kim’s government had shunned millions of vaccine shots offered by the U.N.-backed COVAX distribution program, likely because of international monitoring requirements attached to them.

It has so far ignored rival South Korea’s offer to provide vaccines, medicine and health personnel, but experts say the North may be more willing to accept help from its main ally China. South Korea’s government said it couldn’t confirm media reports that North Korea flew multiple planes to bring back emergency supplies from China on Tuesday.

North Korean officials during Tuesday’s meeting continued to express confidence that the country could overcome the crisis on its own, with the Politburo members discussing ways for “continuously maintaining the good chance in the overall epidemic prevention front,” KCNA said.

While Kim was seen wearing masks for the first time following North Korea’s admission of COVID-19 infections last week, state media photos of Tuesday’s meeting showed Kim and Politburo members engaging in discussions barefaced, in a possible expression of confidence.

Yksi iso mutta: jos löytyy alue, jossa ei ole rokotekattavuutta ja jostain syystä ei luonnollisenakaan sairastetun pandemian aiheuttamaa immuunivastetta - entä sitten? ja löytyyhän sitä: Pohjois-Korea!

https://www.science.org/content/article/malignant-fever-covid-19-surges-north-korea

A ‘malignant fever’—COVID-19—surges in North Korea

Aid agencies develop plans to help if the country requests it

 

 Sitaatti: 

Over the weekend, when Kee Park saw the latest figures on what North Korea calls a “malignant fever” sweeping the country, he realized how dark the outlook had become. New cases of the illness—almost certainly COVID-19, caused by the Omicron variant of SARS-CoV-2—appear to be doubling every 2 days in the last significant population in the world, some 25 million people, that has no immunity to the disease from vaccination or infection.

“The outbreak is now nationwide,” says Park, a global health specialist at Harvard Medical School. “We’re looking at a major, major catastrophe.”

Aid agencies are gearing up for a robust response—if North Korea is willing to open its doors. The North Korean government has ignored past offers of COVID-19 vaccines, presumably to avoid international monitoring of vaccine distribution, humanitarian experts who have worked in North Korea say. But they believe the crisis—which North Korea’s leader Kim Jong Un has acknowledged is causing a “great upheaval”—will in the coming days persuade the reclusive nation to request assistance. In the meantime, they are compiling a list of what will be needed to combat the outbreak, which organizations could provide those items, and how to get them into North Korea.

Early in the pandemic, North Korea closed itself off from the world in a bid to keep the virus at bay. That strategy largely succeeded for 2 years, despite occasional reports of possible outbreaks that authorities managed to snuff out. Until last month the country, hampered by shortages of reagents, had tested just 66,000 people for COVID-19 and reported zero cases.

But now the Korean Central News Agency, a government outlet, has reported that new cases of presumptive COVID-19 have skyrocketed from 18,000 on 12 May to 392,920 on 15 May, including several confirmed as caused by the BA.2 Omicron subvariant. Since late April, North Korean health authorities have tallied more than 1.2 million cases of symptomatic illness and 50 deaths, including six children. “That’s 5% of the population with symptoms,” says Park, who directs Harvard’s Korea Health Policy Project and has made more than 20 trips to North Korea since 2007. “And the slope of new cases is on its way up. We’re not anywhere near the plateau.” Assuming a conservative mortality rate from Omicron of 1%, the death toll from the current case number could exceed 12,000, he says.

North Korean officials have ordered a nationwide lockdown that confines people to their homes or workplaces, and students to their dorms. The lockdown has also severed communications between international agencies and local staff. But there’s no doubt that the country is ill-prepared to cope with COVID-19. Going into the pandemic, its health care system ranked 193rd in the world, and it has struggled to combat other infectious diseases such as tuberculosis and maintain food security, a challenge exacerbated by a widespread drought this spring.

If North Korea embraces outside assistance, topping Park’s list as a potential lifesaver is Paxlovid. The antiviral would reduce the number of patients who get seriously ill or die, easing the burden on North Korea’s frail health system, he notes. But it needs to be taken within 5 days of diagnosis, so health workers will have to respond fast to new cases. He and other experts also cite rapid diagnostic tests as a high priority, and food to boost nutritional status—and thus the body’s immune response. “We need to fast track the aid,” Park says.

First, though, North Korea will have to accept it