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| Clinical Management of HIV Drug Resistance (Photo credit: AJC1) |
Lemon lime (rinse) Citrus –leading cause of stimulation in the immune cells; prevention of infection- hygienic
CD4 receptors binding
Gp160-gp 120-gp41 -pg9 -pg 16-microscopic criteria and active in gene results.
The microscopic criteria is met in the administration of the effects of the citrus in aids patients as a cleansing technique. The efficiency of a system of molecular biology to circumvent the entire spectrum of science and medicine the related imagery and the experiments that are crucial to the discovery of a gene.
Theoretical Concepts
The mechanisms which include:
The targeted delivery of a protein
The interaction between an antibody and a receptor
The signalling and communication which renders a cell non compliant
Communication between anti viral bodies
Drug resistant counters such as identifying the threat/problem dealing with the specific switch or mechanism which is involved in creating the process so the cell or virus can become drug resistant and resolving that issue.
Finding ways to control the impulse.
Separation from the receptor that provides the cell with enough criteria to propagate
The prevention of disease states by the immediate and programmed dissemination of matter microscopic and macroscopic
The disintegration of trace elements left after the dispersal of the tumours.
Counteracting any negative results through gene splicing repair regeneration sequencing and reconstruction restructuring the DNA RNA to provide a link to healing mechanisms in the body
Connective stem cell research and blood utilization for antibodies and cures.
The dispersal of antibodies that succumb the viral cells and eliminate them.
By dissection by segregation by destroying key elements which allow the virus to function spread and infect the host.
Anti viral drugs and anti viral treatments that halt the progression and instil mechanisms which cause the body to heal itself
Extracts from exacting proteins elements and enzymes antibodies which prevent any further disease progression
Research innovation and details of approaches environment and ecosystems habitats and diets exercise sleep and overall health
Cleansing the body system of any infection diverting the source of nutrition to the affected area, cells or stages of tumour progression relinquishing control of the virus to a manageable state
Going from advanced stages to manageable symptoms to disease cure
Looking at the mechanisms which infer a state of ill health the possibilities of treatment by introducing the medicinal benefits of certain criteria such as natural chemical inorganic organic and synthetic
Some metals are also known to carry healing properties such as research done with microtubules and nano-tubes and their application to medicine.
References :
IHOP NCBI PubMed
To little stomach acid-orange juice/Glutanic acid with Delavirdine
July 8, 1996
Use of lemon juice and lemon grass for the treatment of oral candidiasis in an HIV population validated by randomizied controlled trial
March 16,2009
Study on HIV
Replication cycle
Prevention of individual protein release (HIV proteins) prevention of release of viral RNA and proteins. Immobilization dissemination prevention of movement in cell surface. Analysis of immature virus examination for consistency cell division meiosis mitosis etc. experimentation and prevention of division.
Prevention of new viral DNA to be used as genomic DNA. DNA and analysis of amino acids for the prevention of making viral proteins
Analysis and movement the regression and the stoppage of viral DNA being transported across the nucleus sharing of the link that integrates it to host DNA. Prevention of coupling sequencing intervention
Reverse transcription analysis and deconstruction the prevention of the formation of viral DNA
Blockage of the host cell to HIV RNA reverse transcription integrase and other viral proteins.
Prevention of fusion of the HIV cell to the host surface
The viral core- structure of HIV
P7 HIV Nucleocapsid Protien
The reversal of the process of production three enzymes reverse transcriptase integrase and protease the production of these examined the protein P17 HIV Matrix protein that lies between the viral core and the viral envelope changing its use and productivity
The ends of each strand of HIV contain an RNA sequence of LTR long terminal repeat to be switched off as proteins from HIV and host cell are configured to either support its non active switch or non existent so the switch is’nt activated
HIV has 6 regulatory cases TAT REV NEF VIF VER VPU
NEF replication VPU release of new particles from infected cells VIF the protein encoded by VIF gene interacts with an antiviral protein in host cells APOCEL3G
Causing inactivation of the antiviral effect and enhancing HIV replication
NEF-reversal of meiosis mitosis etc.
VEU- stoppage of virus –control of metastisis
VIF the counteracting of the protein or the process
Viral protein P-24- 2000 copies in capsid reverse process of contents to single strands of HIV RNA each with a copy of the viruses genes
3 structural genes GAG POL and ENV the complete reversal of the processes of RNA with encoding the reversal process for viral RNA delivery
Makes structural proteins from new virus particles
ENV-gp160->gp120gp41 broken down by a viral enzyme- counteract the enzyme and have usage for the opposite of gp120 and gp41
Spherical in shape or whatever shape is most useful the diameter will be evaluated HIV- 1/10,000 of a millimetre, outer coating antibody and opposite of viral envelope
Lipids replaced by antiviral entities protiens from the host cell are replaced by proteins from the opposite of HIV 72 copies of ENV replaced by microscopic proteins that counteract the HIV process
Envelope proteins<->antiviral processes
HIV evades the immune system usage of holograms as diverse and varied as needed for productivity and analysis to adapt to the constantly changing HIV overall monitoring system to keep in check new and diverse strains.
HIV devastates the immune system
HIV prevention of destroying precursor cells perhaps with stem cell treatments and replacement therapies
Management of development of precursor cells into mature immune cells
Protection of the bone marrow and the thymus inducing regeneration in both
Prevention of immune suppression
Prevention of the HIV cells binding to the cell surface CD8 T cells controlled and only deployed when necessary
Prevention (and proper inducement) of apoptosis- cells not infected with HIV-no apoptosis
Cells infected-apoptosis with dissemination dissolving and disintegration
Blood stream and lymph nodes controlling apoptosis
CD$+T cells rid of infection of HIV prevention of the virus of infected cells form budding. Normal activities of the cell looked at /regulated.
Other infections immune system CD4+T cells regeneration to fight infections
HIV hides from the immune system
Disinfection of the cytoplasm cleansing of the chromosomes
Latent reservoirs looked at examined and determined to be rid of all infective materials
Brain lymph nodes reticulo-endothelial system bone marrow gastrointestinal cells checked and virus subjugated to inert status by riddance of infective agents in these places
Reorganization of anti retroviral drugs to accommodate latent reservoirs
Clinical progression of HIV
CD4+T cells prevention of replication HIV copies viral load prevention of metastasis thymus spleen lymph nodes genetic material of the cell protected from integration of the virus examination of acute phase latency
Examination for flu-like symptoms
CD4+T cells regulation and (additives to fight infection to antibodies)modified CD$+T cells regulated(2to4 weeks)
Prevention of replication in the lymphoid organs
Prevention of increase of viral load in blood
Regulation of CD4+Tcells
Prevention of further infections
Factors that affect disease progression
CCR5 +CD4 molecule prevention of infection of cells
CXCR4 prevented from entering a cell a look at mutations-examination
CXCR4 prevented from entering a cell a look at mutations-examination
HIV in blood viral load controlled by cleansing of the blood transfusions etc
HAART highly active antiretroviral therapy introduced okays
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