occupational health considerations for working with viral ... · parvoviridae (aav) ......
TRANSCRIPT
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Occupational Health Considerations for Working with Viral Vectors in the Research Laboratory
Dawn P. Wooley, Ph.D., SM(NRCM), RBP, CBSP
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Outline
Introduction Viruses and Vectors Specific viruses:
Retroviridae Adenoviridae Poxviridae Parvoviridae (AAV) Herpesviridae
Occupational Health: Clinical presentation Pathogenesis Diagnostic Tests Transmission Epidemiology Treatments Prevention
Conclusion
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Occupational Health – Ideal World
Laboratory workers visit the occupational physician prior to beginning work.
They complete a confidential medical questionnaire to identify any relevant medical conditions.
Workers are sent back to employer with a list of restrictions, if any, that does not identify their medical condition.
Workers are offered pre-exposure immune surveillance and vaccinations as appropriate.
Emergency plans are in place and workers are trained on how to handle an exposure event, including PEP.
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Occupational Health – Real World
Laboratory workers never see an occupational physician or are denied access to one.
Workers complete a detailed medical history and fax it to their EHS office.
Appropriate medical restrictions not identified. Workers not offered pre-exposure immune surveillance
or vaccinations. No emergency plans, miss opportunity for post-exposure
prophylaxis, wait in local emergency room for 4 hours.
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Post-Exposure Prophylaxis
Definition: Treatment to prevent disease afteran exposure has already occurred.
Has historically worked well with viruses that have a long incubation period, e.g. Rabies virus, Hepatitis B virus.
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Virus
Obligate, intracellular parasites. They are unable to grow and divide on their own. Cannot generate energy.
Have a variety of methods to commandeer the functions of the host cells to direct their own replication scheme, often at the expense of the host cell.
Researchers attempt to harness the power of these organisms to deliver nucleic acids to turn them into gene delivery tools.
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Replication Defective Viruses
To avoid potential pathogenicity of viral vectors, it is desirable to disable them so they cannot replicate in target cells.
This is generally accomplished by deleting genes that provide necessary trans-acting functions from the vector genome.
Introduction of these genes and defective vector into cells results in the synthesis of vector genomes and packaging of the defective genomes into virus particles.
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Vectors Used in Gene Therapy Trials
Sheridan C. 2011. Nature Biotechnology. 29(2):121-128
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Retroviridae (7 genera)
Alpharetrovirus ALV, RSV
Betaretrovirus MMTV
Gammaretrovirus MLV FeLV, SNV, XMRV*
Deltaretrovirus HTLV I and II, BLV
Epsilonretrovirus WDSV
Lentivirus HIV SIV
Spumavirus HFV, SFV
*New
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Lentivirus is a genus, not a species
Family: Retroviridae Genus: Lentivirus (9 species)
Human immunodeficiency virus 1 (human) Human immunodeficiency virus 2 (human) Simian immunodeficiency virus (monkey) Bovine immunodeficiency virus (cow) Equine infectious anemia virus (horse) Caprine arthritis encephalitis virus (goat) Visna/maedi virus (sheep) Puma lentivirus (puma) Feline immunodeficiency virus (cat)
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Xenotropic Murine Leukemia Virus-Related Virus (XMRV)
Newly discovered in 2006
Conflicting Reports: Associated with Prostate Cancer and Chronic
Fatigue Syndrome
Concerns for transplants and blood donation
Urisman, A., et al. 2006. PLoS Pathogens. 2(3):0211-0225.
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Retroviral Host Range
Ecotropic: viruses that are only able to infect the species originally isolated from.
Xenotropic: viruses that are unable to infect the species originally isolated from.
Amphotropic: viruses that are able to infect multiple species of cells, including human.
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Tropism
Viral preference for a particular cell type
Often dictated by the viral envelope or capsid proteins and by receptors on the host cell
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HIV-1 Virion
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gag pol
LTRenv
LTRMLV
HIVLTR LTR
polvif nef
vpuvprenvrev
gag
Retroviral Genomes
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Basic Genes
Gag: Nucleocapsid-core(MA, CA, NC)
Pol: RT, protease, integraseEnv: Surface glycoprotein
(SU and TM)
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Additional Lentivirus Genes
Regulatory Genes tat rev
Accessory Genes vif vpr vpu nef
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Clinical Presentation of HIV-1
Asymptomatic Acute infection Persistent generalized lymphadenopathy Other disease
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Pathogenesis of HIV
AIDS Immunodeficiency Opportunistic infections and cancers Neurological disease (AIDS dementia
complex)
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Transmission of HIV
Wild-type Restricted tropism Blood products Sexual transmission Vertical transmission
HIV vector virus in the laboratory Broadened tropism Concentrated virus Parenteral Droplet contact
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HIV Testing
Antibody Testing Blood, Oral Fluid, Urine ELISA/EIA Western blot
Antigen Testing p24 antigen test, 1996-2003 by blood banks
Nucleic Acid Amplification Testing (NAT) Direct detection, minipool, 2002 by blood banks Viral load assay for patient (prognostic)
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Rapid or Point-of-Care Tests
Cost < $10 20-30 minutes Several on the market Plasma, serum, whole blood, oral fluid Require confirmatory test, if positive
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Home Tests
Home Access Express HIV-1 Test 1996, FDA approved Mail-in blood test
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Seroconversion—Exposure to a sufficient dose of HIV vector virus would likely score positive on a screening test.
Antibody Testing: Blood, Oral Fluid, Urine ELISA/EIA (Screening) Western blot (Confirmatory)
Modern diagnostic kits generally use recombinant proteins or peptides, including those based on HIV-1 gp160 or gp41, HIV-2 gp36, and HIV-1 p24.
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Western Blot
Exposure to a sufficient dose of HIV vector virus
could score indeterminate (suggestive)
Red arrow indicates presence in vector virus
**
*Antibodies found in experimentally infected animals
Baekelandt, V., et al. 2002. Human Gene Therapy 13:841–853.Abordo-Adesida, E., et al. 2005. Human Gene Therapy, 16:741–751.
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HIV Testing Issues
Social Stigma
Fear
Medical Privacy For both HIV-negative as well as HIV-positive
cases
State reporting and partner notification
"Free" HIV testing sites and record keeping
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Pre- and Post-Exposure HIV Testing: Points to Consider
Wild-type HIV vs. vector
Protecting the institution
Protecting the worker
When to establish the baseline?
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HIV Post-exposure Prophylaxis (PEP)
CDC/WHO recommendation: ASAP, but no later than 72 hrs.
Treatment regime: Consideration of drug-resistant strains
REFERENCES:
CDC. Updated Public Health Service guidelines for the management of health-care worker exposures to HIV and recommendations for postexposure prophylaxis. MMWR 2005;54(No. RR09):1-17.
WHO. Post-exposure prophylaxis to prevent HIV infection--Joint WHO/ILO guidelines on post-exposure prophylaxis (PEP) to prevent HIV infection. WHO, 2007.
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Research Laboratory PEP for HIV for Highly Concentrated Virus Preps Titers now up to 1.4 x 1010 TU/ml1
Wild-type or potentially replication-competent preps, goal is to prevent active infection.
Late generation systems, goal is to prevent integrations, especially with dangerous transgenes, such as oncogenes.
Need emergency plan that includes on-site, rapid access to anti-HIV medications.
1Coleman, J.E., et al. 2003. Physiol Genomics 12: 221–228
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Antiviral Therapy (Drugs)
Reverse Transcriptase Inhibitors Nucleoside: AZT, ddI, and 3TC Nonnucleoside: Nevirapine, Foscarnet
(Phosphonoformic acid)
Protease Inhibitors Ritonavir Indinavir
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Antiviral Therapy (New Drugs)
Entry Inhibitors Fuzeon (2003) – Block gp41; injection only Selzentry (2007) – Blocks CCR5
Integrase Inhibitors Isentress (2007)
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Traditional Combination Drug Therapy
AIDS "Cocktails" or "HAART"(Highly Active Anti-Retroviral Therapy)
2 Reverse Transcriptase Inhibitorsplus
1 Protease Inhibitor
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Total: 34.0 million [31.4 million – 35.9 million]
Western & Central Europe
900 000[830 000 – 1.0 million]
Middle East & North Africa300 000
[250 000 – 360 000]
Sub-Saharan Africa23.5 million
[22.1 million – 24.8 million]
Eastern Europe & Central Asia
1.4 million [1.1 million – 1.8 million]
South & South-East Asia4.0 million
[3.1 million – 5.2 million]
Oceania53 000
[47 000 – 60 000]
North America1.4 million
[1.1 million – 2.0 million]
Latin America1.4 million
[1.1 million – 1.7 million]
East Asia830 000
[590 000 – 1.2 million]
Caribbean230 000
[200 000 – 250 000]
Adults and children estimated to be living with HIV 2011
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Prevention
No Vaccines Screening blood supplies Universal precautions for workers Education about safe sex and drugs
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35
MLV and HIV vector hazards Integration (Insertional Mutagenesis, aka "cancer")
Transgene
High mutation rate
High transduction efficiencies
Broad tropism
Recombination
Endogenous retroviruses
Seroconversion
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Adenoviridae
Genus: Mastadenovirus human adenovirus A-G
(currently, over 50 serotypes in humans)
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70-100 nm
Adenovirus Virion
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Adenovirus under Electron Microscope
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Generations of Adenovirus vectors First Generation Vectors
Two early genes deleted (E1 or E1/E3)
Second Generation Vectors Three early genes deleted (E1, E3, E4) He, T.-C. et al. 1998. PNAS. 95:2509-2514
Third Generation Vectors “Gutless vectors” All viral genes deleted; only essential cis-acting sequences retained
AdenoITR ITR
E3 E4E1
36 kbp
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Pathogenesis Respiratory infection
Particularly seen in children Acute respiratory disease in military recruits Pneumonia in children, recruits, and AIDS
Eye infection Urinary tract infection Gastroenteritis Cancer
Adenovirus Type 12 can cause cancer in hamsters (nonpermissive cells), but not humans
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Diagnosis
Laboratory Analysis
Specimens: Feces, pharyngeal swab, nasopharyngeal aspirate, transtracheal aspirate, bronchial lavage, conjunctival swab, corneal scraping, tears, genital secretions, urine, biopsy tissue (liver, spleen, lung, brain)
Tests: Immunoassay, virus isolation, immunofluorescence to detect antigen
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Epidemiology
Estimated to cause ~10% gastroenteritis in children
Causes ~5-10% of respiratory infections Transmission by oral-fecal route most
common Also transmission by aerosol and water-
borne routes
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Epidemiology (con't)
Highly prevalent serotypes: Ad1, Ad2, Ad3, Ad5, and Ad6 These types infect ~80% of people early in life
Other adenovirus types show an epidemic epidemiology, infecting anyone not previously immune.
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Control and Prevention
Personal hygiene Live vaccine given to military recruits Capsule form by-passes throat Grows in gut and generates immunity
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Adenovirus vector hazards Recombination with wild type strains Recombination during virus production Contamination with helper virus (gutless) E1A deficiency complemented in vivo Transgene Immune response Viral protein toxicity Difficulties in detecting exposure (prevalence) Altered tropism – capsid and fiber proteins
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AAV species
Parvoviridae Family
Genus Parvovirus – cats, dogs, mink Genus Erythrovirus – human; B19 Genus Dependovirus – human; need helper
(adeno-associated virus; AAV; at least 9 serotypes)
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Features of AAV
ssDNA (+ or -), 5 kb genome, non-enveloped Replicate in nucleus of dividing cells (using
cellular enzymes and helper virus) Generally unable to replicate on its own Relatively stable virion Can integrate at 19q13.4 and replicates as a
provirus (Rep-protein dependent) in vitro Not observed to integrate in vivo
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Features of AAV (continued)
Not associated with disease (RG1) Can infect all cells tested so far Can remain latent in an episomal state (in
absence of helper) High transduction frequency Only requires 145 nt ITR for integration No superinfection immunity
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AAV Genome
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AAV Vector Hazards
Helper virus contamination Specific integration requires Rep protein Insertional mutagenesis/cancer Deletion/rearrangement during integration Multiple copies can integrate Reactivation Helper viruses: Adeno, herpes, pox Evidence of autonomous growth
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Poxviridae
Variola virus (smallpox virus) Molluscum contagiosum virus Vaccinia virus* Monkeypox virus Cowpox virus Fowlpox virus* Canarypox virus*
Human
Zoonotic
Avian
*Used as viral vectors
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Vaccinia Virus Vectors
RG2 agent Wide host range Extensively used as a recombinant protein
expression vector Primary in vivo use: expression of antigen to elicit an
immune response Vaccinia virus used as a live vaccine for protection
against smallpox Attenuated strains (Modified Vaccinia Ankara, MVA)1
Replication defective strains (dVV-L)2
1Mayr, A., Hochstein-Mintzel, V., Stickl, H., 1975. Infection 3, 6 –14.2Holzer, G.W., & Falkner, F.G., 1997. J. Virol. 71, 4997–5002
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Orthopoxvirus Parapoxvirus
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Vaccinia Virus Genome
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Epidemiology
Smallpox eradicated in 1977 Molluscum contagiosum virus
Common in Zaire, Papua, and New Guinea Zoonoses rare Transmission by direct or droplet contact
Indirect contact (ex. bedding) less common Rarely via air in enclosed settings Relatively stable in environment
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Control No treatments for smallpox prior to its eradication. Treatments for Vaccine Complications and
Experimentals: Methisazone – Blocks translation of late mRNAs of
poxviruses; used prophylactically against smallpox. Vaccinia Immune Globulin (VIG)
Antibodies from vaccinated people, 1960’s Surgery to remove mass (reduce amount of virus) Eyes: Interferon, vidarabine, trifluridine or acyclovir Cidofovir: Used for CMV; Has shown broad spectrum antiviral
activity against all DNA viruses. Supportive care
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Smallpox Prevention Dryvax, live vaccinia virus in dried form
First approved 1931, existing doses1970's & 80's New 100-dose kit approved October 2002 NYC Board of Health Strain, Wyeth Lab
ACAM2000 Approved in 2007 Live attenuated, clone of Dryvax strain / grown in
Vero Cells Quarantine and contraindication issues Complications, including inflammation in
around the heart and brain, others (see next)
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Normal Vaccine Timeline
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Satellite Lesion Lymphangitis
Cellulitis Edema
Normal Vaccine Variants
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Generalized vaccinia
Vaccine Complication
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Ocular vaccinia
Vaccine Complication
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Eczema vaccinatum
Vaccine Complication
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Progressive vaccinia(fatal)
Vaccine Complication
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Avipox Vectors
Replication competent.
Poxviruses that productively infect avian species (fowlpox and canarypox) are replication defective in mammalian cells, will direct early gene expression.
May be a safer alternative to vaccinia-based vectors for in vivo applicatons.
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Herpesviridae
Human herpesvirus 1 (Herpes simplex virus 1)* Human herpesvirus 2 (Herpes simplex virus 2) Human herpesvirus 3 (Varicella-zoster virus) Human herpesvirus 4 (Epstein-Barr virus)* Human herpesvirus 5 (Human cytomegalovirus) Human herpesvirus 6 Human herpesvirus 7 Human herpesvirus 8 (Kaposi’s sarcoma virus)
Roseola viruses
*More commonly used as viral vectors
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Herpesviruses
RG2 agents
Dual life cycle: Lytic growth in epithelial cells Latent infection in neuronal cells
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Herpesvirus Genome
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Types of Herpes Virus Vectors
Conditionally replicating Gene deletion renders the virus able to replicate in vitro but it is
compromised in vivo
Replication defective Deletion of essential genes Requires helper function (i.e. complementing cell)
Amplicon Systems Vector contains the minimal cis-acting signals for viral genomic
replication Requires helper virus or complementing cell Cosmids or artificial bacterial chromosomes also used to produce
the virus
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Herpesvirus Pathogenesis
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Epidemiology and Transmission
Overall, herpes viruses are highly prevalent (i.e. high seropositivity in the general population)
Transmission Contact Saliva Airborne Blood
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Control and Prevention
Control Acyclovir (and its newer derivatives) Ganciclovir Foscavir
Prevention Vaccine (HHV-3)
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NIH Requirements
Section II-A-2: Personnel may need periodic medical surveillance to ascertain fitness to perform certain activities; they may also need to be offered prophylactic vaccines and boosters (see Section IV-B-1-f, Responsibilities of the Institution, General Information).
Section IV-B-1-i. Determine the necessity for health surveillance of personnel involved in connection with individual recombinant DNA projects; and if appropriate, conduct a health surveillance program for such projects. The institution shall establish and maintain a health surveillance program for personnel engaged in large-scale research or production activities involving viable organisms containing recombinant DNA molecules which require BL3 containment at the laboratory scale. The institution shall establish and maintain a health surveillance program for personnel engaged in animal research involving viable recombinant DNA-containing microorganisms that require BL3 or greater containment in the laboratory.
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Conclusions
Occupational health screening for laboratory workers investigating viral vectors in research laboratories has been generally neglected
Consider pre-exposure screening policy for viruses not highly prevalent (i.e. HIV)
Protection works both ways (institution vs. individual)
Consider the morale issue and creating a culture of safety
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Conclusions (continued)
Always consider the transgene Be aware of the symptoms of the agent being
investigated Always keep in mind characteristics of the
wild-type virus and the potential of the vector to recombine and form replication competent virus
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Questions?
“The difficulty lies, not in the new ideas, but in escaping from the old ones, which ramify, for those brought up as most of us have been, into every corner of our minds.”
John Maynard Keynes (1936)