A modified form of HIV is being tested as a potential treatment for cancer. Researchers are removing patients' T-cells and using HIV to insert genes that program the cells to recognize and attack cancer. The modified T-cells are multiplied and reinfused into patients, where they act like "serial killers" against the cancer cells. In initial tests, two patients saw their cancers drastically reduced or eliminated, with up to five pounds of tumor cells disappearing. The modified T-cells have also been shown to persist in the body for over a year, reactivating to kill new cancer cells. One six-year-old girl with leukemia that was not responding to other treatments saw her cancer go into remission after this experimental HIV therapy
The human immunodeficiency virus (HIV) is a lentivirus (a subgroup of retrovirus) that causes HIV infection and over time acquired immunodeficiency syndrome (AIDS).
The lecture gives concise review about the main four groups of viruses causing hemorrhagic fever i.e. Flavivirues, Filoviruses, Arenaviruses and Bunyaviruses.
Viral hepatitis is the leading cause of liver cancer and the most common reason for liver transplantation
In the United States, an estimated 1.2 million Americans are living with chronic Hepatitis B and 3.2 are living with chronic Hepatitis C
Many do not know they are infected
Each year an estimated 21,000 persons become infected with Hepatitis A; 35,000 with Hepatitis B, and 17,000 with Hepatitis C
Hepatitis A – fecal/oral, contaminated food, vaccine available
Hepatitis B – blood, semen, vertical (mother-child), vaccine available
Hepatitis C – blood (IV drug use, transfusion, organ donation, unsterile injecting equipment, sexual intercourse)
Hepatitis D – survives only in cells co-infected with hepatitis B
Hepatitis E* – contaminated food or water, fecal/oral
*causes short-term disease and is not a chronic carrier state
The human immunodeficiency virus (HIV) is a lentivirus (a subgroup of retrovirus) that causes HIV infection and over time acquired immunodeficiency syndrome (AIDS).
The lecture gives concise review about the main four groups of viruses causing hemorrhagic fever i.e. Flavivirues, Filoviruses, Arenaviruses and Bunyaviruses.
Viral hepatitis is the leading cause of liver cancer and the most common reason for liver transplantation
In the United States, an estimated 1.2 million Americans are living with chronic Hepatitis B and 3.2 are living with chronic Hepatitis C
Many do not know they are infected
Each year an estimated 21,000 persons become infected with Hepatitis A; 35,000 with Hepatitis B, and 17,000 with Hepatitis C
Hepatitis A – fecal/oral, contaminated food, vaccine available
Hepatitis B – blood, semen, vertical (mother-child), vaccine available
Hepatitis C – blood (IV drug use, transfusion, organ donation, unsterile injecting equipment, sexual intercourse)
Hepatitis D – survives only in cells co-infected with hepatitis B
Hepatitis E* – contaminated food or water, fecal/oral
*causes short-term disease and is not a chronic carrier state
HIV ITS PREVENTION AND CONTROL is a presentation that aim to introduce HIV(Human immunodeficiency Virus),its pathogenesis, clinical manifestation, diagnosis, treatment, prevention and control
presentation talking about streptococcus pneumonia ,identification of streptococcus pneumonia ,virulence factors of streptococcus pneumonia and mechanism of pathogenesis
teaching support for 2nd year medical school students: steps of the laboratory diagnosis of infections caused by bacteria of the genera Staphylococcus and Streptococcus
It Contains Pathogenesis of viral diseases like AIDS, Hepatitis, Influenza and Rabies.
It contains detail pathogenesis with various verified sources.
You can refer references to visit the sources used.
Handout materials compiled by Dr. Ananda Balayogi Bhavanani for the SEMINAR-CUM-WORKSHOP ON YOGA AND COMPLEMENTARY THERAPIES FOR AIDS/HIV organised by the Advanced Centre for Yoga Therapy Education & Research (ACYTER), JIPMER for medical & paramedical professionals and yoga therapists at JIPMER, Pondicherry. The event was held on 30th January 2010 at the Multipurpose Hall, JIPMER Nursing College, JIPMER, Pondicherry-6.
AIDS is a syndrome in which the body undergoes the loss of cellular immunity which lower the body’s ability to fight against disease. The cause of AIDS is a retrovirus called Human Immunodeficiency Virus HIV . The symptoms of AIDS usually start from 3 6 weeks and are mild symptoms like fever, rash, swollen glands, and body ache which are followed by characteristic AIDS symptoms which may appear within 10 years of infection. In world till 2017 genome sequencing of the virus, sub typing of the virus, recombinant forms of the virus has been deeply discovered and studied which helps in better diagnosis and in choosing the strategies for treatment. The objective of this review is to give a brief history and current picture of HIV prevalence and describe its pathophysiology and modes of transmission. And how it is diagnosed, sign and symptoms, treatment and how it can be prevented. Ch. Teshil Maring | Gaurav Kumar Sharma | Kaushal Kishore Chandrul "A Review: AIDS" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-5 | Issue-5 , August 2021, URL: https://www.ijtsrd.com/papers/ijtsrd45188.pdf Paper URL: https://www.ijtsrd.com/other-scientific-research-area/other/45188/a-review-aids/ch-teshil-maring
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
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Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
2. RETROVIRUS
A retrovirus is an RNA virus that replicates in a
host cell through the process of reverse
transcription. First it uses its own reverse
transcriptase enzyme to produce DNA from its
RNA genome, reverse of the usual pattern, thus
retro (backwards). This new DNA is then
incorporated into the host's genome by an integrase
enzyme.
3. The following genera are included here:
Genus Alpharetrovirus; type species: Avian leukosis
virus; others include Rous sarcoma virus
Genus Betaretrovirus; type species: Mouse mammary
tumour virus
Genus Gammaretrovirus; type species: Murine leukemia
virus; others include Feline leukemia virus
Genus Deltaretrovirus; type species: Bovine leukemia
virus; others include the cancer-causing Human T-
lymphotropic virus
Genus Epsilonretrovirus; type species: Walleye dermal
sarcoma virus
Genus Lentivirus; type species: Human
immunodeficiency virus 1; others include Simian, Feline
immunodeficiency viruses
Genus Spumavirus; type species: Simian foamy virus
4. According to Baltimore’s classification they are:
Group VI viruses
All members of Group VI use virally encoded reverse transcriptase, an RNA-
dependent DNA polymerase, to produce DNA from the initial virion RNA
genome. This DNA is often integrated into the host genome, as in the case of
retroviruses and pseudoviruses, where it is replicated and transcribed by the
host.
Group VI includes:
Family Metaviridae
Family Pseudoviridae
Family Retroviridae - Retroviruses, e.g. HIV
Group VII viruses
Both families in Group VII have DNA genomes contained within the invading
virus particles. The DNA genome is transcribed into both mRNA, for use as a
transcript in protein synthesis, and pre-genomic RNA, for use as the template
during genome replication. Virally encoded reverse transcriptase uses the pre-
genomic RNA as a template for the creation of genomic DNA.
Group VII includes:
Family Hepadnaviridae - e.g. Hepatitis B virus
Family Caulimoviridae - e.g. Cauliflower mosaic virus
5. NOW HIV…….
Human immunodeficiency virus (HIV) is a lentivirus (slowly
replicating retrovirus) that causes acquired
immunodeficiency syndrome (AIDS), a condition in humans
in which progressive failure of the immune system allows life-
threatening opportunistic infections and cancers to thrive.
Infection with HIV occurs by the transfer of
blood, semen, vaginal fluid, pre-ejaculate, or breast milk.
Within these bodily fluids, HIV is present as both free virus
particles and virus within infected immune cells.
8. BRIEF HISTORY…..
AIDS was first clinically observed in 1981 in the United
States. The initial cases were a cluster of injection drug users
and gay men with no known cause of impaired immunity who
showed symptoms of Pneumocystis carinii pneumonia
(PCP), a rare opportunistic infection that was known to occur
in people with very compromised immune systems. Soon
thereafter, additional gay men developed a previously rare
skin cancer called Kaposi's sarcoma (KS).
Both HIV-1 and HIV-2 are believed to have originated
in non-human primates in West-central Africa and to have
transferred to humans (a process known as zoonosis) in the
early 20th century. HIV-1 appears to have originated in
southern Cameroon through the evolution of
SIV(cpz), a simian immunodeficiency virus (SIV) that infects
wild chimpanzees (HIV-1 descends from the SIVcpz endemic
in the chimpanzee subspecies Pan troglodytes troglodytes)
9. Left to right: the African green monkey source of SIV, the sooty
mangabey source of HIV-2 and the chimpanzee source of HIV-1
10. ABOUT VACCINE….
Washington -The hunt for an HIV vaccine has
gobbled up $8bn in the past decade, and the
failure of the most recent efficacy trial has
delivered yet another setback to 26 years of
efforts.
With the next attempts expected to be years
away, top researchers now say there is a "void"
or a "gap" in current clinical trial efforts to test
whether a vaccine may be safe and effective in
people.
11. BRIEF FACTS…..
How quickly do people infected with HIV develop
AIDS?
The length of time can vary widely between individuals. The
majority of people infected with HIV, if not treated, develop
signs of HIV-related illness within 5-10 years, but the time
between infection with HIV and being diagnosed with AIDS can
be 10–15 years, sometimes longer. Antiretroviral therapy
can slow down disease progression to AIDS by decreasing the
infected person’s viral load.
12. Primary HIV infection - may be asymptomatic or experienced
as Acute retroviral syndrome.
Clinical stage 1 – asymptomatic or generalized swelling of the
lymph nodes
Clinical stage 2 - includes minor weight loss, minor
mucocutaneous manifestations, and recurrent upper respiratory
tract infections
Clinical stage 3 - includes unexplained chronic
diarrhoea, unexplained persistent fever, oral candidiasis or
leukoplakia, severe bacterial infections, pulmonary
tuberculosis, and acute necrotizing inflammation in the mouth.
Some persons with clinical stage 3 have AIDS.
Clinical stage 4 - includes 22 opportunistic infections or cancers
related to HIV.
All persons with clinical stage 4 have AIDS.
Most of these conditions are opportunistic infections that can be
treated easily in healthy people.
17. HIV AS A REMEDY…..
The HIV virus may be about to become a new weapon
in the fight against cancer as initial tests have shown it
can drastically minimize and even help cure the most
common form of leukemia.
A research team, led by Dr. Carl June working out of
the Abramson Cancer Center at the University of
Pennsylvania, has been experimenting with using a
harmless version of the HIV virus combined with
genetically modified white blood cells as a new way to
fight cancer. The cells are taken from patients and
modified with new genes that make them target
cancer cells, but just as importantly, they can also
multiply once injected allowing them to scale up as a
small army inside the body.
18. HOW?
.
1. Doctors run the patient’s blood through a machine that
removes T-cells, but returns the rest of the blood to the
patient. T-cells are virus and cancer fighting white blood
cells.
2. A modified form of the HIV virus is used to infect the T-
cells and insert genes that cause it to recognize and attack a
particular cancer, then multiply and survive in the patients for
months.
N.B :
The modified HIV virus carries what Carl June, one of the
doctors involved, called a "Rube Gol dber g-l i ke
sol ut i on“, in an interview with the New York Times. The
virus carries DNA from humans, mice and cows, a virus that
infects woodchucks, and one that infects cows.
19.
20. The modified T-cells then carry chimeric antigen
receptors, proteins which allow them to recognize and kill
multiple cancer cells.
3. Chemotherapy kills any remaining T-cells in the patient.
The doctors don't want un-modified T-cells impeding the new
ones.
4. The modified T-cells are returned to the patient. Within the
patient the newly re-programmed T-cells proliferate.
5. Over the next few weeks the patient develops a
temperature, chills, shakes, low blood pressure, and other
flu-like symptoms. The symptoms are caused by chemicals
called cytokines produced by the T-cells.
The flu-like symptoms also mean the cancer is on the run.
After the ordeal, doctors estimated that two pounds of
cancer cells had died off in one patient, William Ludwig.
21.
22. The results have surprised everyone. These
modified cells have acted like serial
killers, multiplying and killing all of the cancer
cells in two patients, while reducing them by
70% in a third. The equivalent of five pounds
of cancer cells has disappeared from each
patient. More good news stems from the fact
that the modified cells remain in the body and
have been seen to reactivate and kill new
cancer cells as long as 12 months after they
were first injected.
23. ABOUT A GIRL CURED USING THIS EXPERIMET…..
In April this year, Emily Whitehead's family had almost given
up hope.
The brave six-year-old had been fighting leukaemia for two
years, only to relapse for a second time during intensive
chemotherapy treatment in February.
Doctors had exhausted all the traditional treatments as Emily
could not remain in remission for long enough to attempt a
bone marrow transplant. So her desperate parents, Kari and
Tom, started looking at more radical options.
N.B: Video on you-tube