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PRESENTED TO,
Mrs. URMILA MISHRA
PRESENTED BY,
Mr. SAGAR KAMBLE
 Immunity is the balanced state of having adequate
biological defenses to fight infection, disease, or other
unwanted biological invasion, while having
adequatetolerance to avoid allergy, and autoimmune
diseases.
 Immunology is a branch of biomedical science that
covers the study of all aspects of the immune
system in all organisms.
Infection
Invasion and multiplication of microorganisms in body
tissues, as in an infectious disease.
Lymphocytes of the Immune System
B Lymphocytes:
Immunocompetency occurs in bone marrow
Produce Antibodies
Conduct Humoral Immunity
T Lymphocytes:
Immunocompetency occurs in thymus
Non antibody producing cells
Conduct Cellular Immunity
 Antibody Mediated
Immunity
 Helper T cells recognize non
self antigens and stimulate B
cells to produce antibodies
 B cells release antibodies
which bind to non self antigens
present on infected cells
 B cells complete their
maturation upon binding to non
self antigens and destroying
infected cells
 Cell Mediated
Immunity
 Macrophages
phagocytize pathogens
 Upon phagocytosis
macrophages present
non self antigens on
their membranes
 Helper T cells recognize
non self antigens and
recruit cytotoxic T cells
 Cytotoxic T cells destroy
infected cell
“Human Immunodeficiency Virus”
A unique type of virus (a retrovirus)
Invades the helper T cells (CD4 cells) in the
body of the host (defense mechanism of a
person)
Threatening a global epidemic.
Preventable, managable but not curable.
Former names of the virus include:
• Human T cell lymphotrophic virus (HTLV-III)
• Lymphadenopathy associated virus (LAV)
• AIDS associated retrovirus (ARV)
 “Acquired Immunodeficiency Syndrome”
 HIV is the virus that causes AIDS
 Disease limits the body’s ability to fight
infection due to markedly reduced helper T
cells.
Patients have a very weak immune system
(defense mechanism)
Patients predisposed to multiple
opportunistic infections leading to death.
 Acquired immunodeficiency syndrome (AIDS)
is a term which applies to the most advanced
stages of HIV infection. It is defined by the
occurrence of any of more than 20
opportunistic infections or HIV-related cancers.
 Persons with positive HIV serology who have
ever had a CD4 lymphocyte count below 200
cells/mcL or a CD4 lymphocyte percentage
below 14% are considered to have AIDS.
Blood products
Semen
Vaginal fluids
 Sharing Needles
• Without sterilization Increases the chances of
contracting HIV
Unsterilized blades
Unprotected Intercourse
 Oral
 Anal
Before Birth
During Birth
Short, flu-like
illness - occurs
one to six weeks
after infection
 Mild symptoms
 Infected person
can infect other
people
Lasts for an average of ten years
This stage is free from symptoms
There may be swollen glands
The level of HIV in the blood drops to
low levels
HIV antibodies are detectable in the
blood
The immune system deteriorates
Opportunistic infections and cancers
start to appear.
The immune
system weakens
too much as CD4
cells decrease in
number.
CD4<500
Bacterial infections
Tuberculosis (TB)
Herpes Simplex
Herpes Zoster
Vaginal candidiasis
Hairy leukoplakia
Kaposi’s sarcoma
CD4<200
Pneumocystic carinii
Toxoplasmosis
Cryptococcosis
Coccidiodomycosis
Cryptosporiosis
Non hodgkin’s
lymphoma
CD4 <50
Disseminated mycobacterium avium
complex (MAC) infection
Histoplasmosis
CMV retinitis
CNS lymphoma
Progressive multifocal
leukoencephalopathy
HIV dementia
 TB is the most common opportunistic infection in HIV and
the first cause of mortality in HIV infected patients (10-
30%)
 10 million patients co-infected in the world.
 Immunosuppression induced by HIV modifies the
clinical presentation of TB :
1. Subnormal clinical and roentgen presentation
2. High rate of MDR/XDR
3. High rate of treatment failure and relapse (5% vs < 1% in HIV)
HIV enzyme-linked immunosorbent
assay (ELISA)
Screening test for HIV
Sensitivity > 99.9%
Western blot Confirmatory test
Speicificity > 99.9% (when combined with
ELIZA)
HIV rapid antibody test Screening test for HIV
Simple to perform
Absolute CD4 lymphocyte count Predictor of HIV progression
Risk of opportunistic infections and AIDS when
<200
HIV viral load tests Best test for diagnosis of acute HIV infection
Correlates with disease progression and
response to HAART
Urine Western Blot
• As sensitive as testing blood
• Safe way to screen for HIV
• Can cause false positives in
certain people at high risk for
HIV
Orasure
• The only FDA approved
HIV antibody.
• As accurate as blood
testing
• Draws blood-derived fluids
from the gum tissue.
• NOT A SALIVA TEST!
Class of Antiretroviral Drug Drug Names
Nucleoside or nucleotide reverse
transcriptase inhibitors (NRTIs)
Abacavir, emtricitabine (FTC), zidovudine (AZT), didanosine
(DDI), zalcitabine (DDC), lamivudine (3TC), tenofovir
(disoproxil fumarate), and stavudine (D4T)
Nonnucleoside reverse transcriptase
inhibitors (NNRTIs)
Efavirenz (EFV), etravirine, nevirapine, and
delavirdine
In clinical trials: Rilpivirine, GSK2248761 (Viiv) and RDEA806
(Ardea)
Protease inhibitors (PIs) Amprenavir, atazanavir, darunavir, fosamprenavir,
indinavir, lopinavir/ritonavir, nelfinavir (NFV),
ritonavir, saquinavir, and tipranavir
Pharmacokinetic Enhancers Ritonavir
In clinical trials: Cobicistat
Fusion entry inhibitors Enfuvirtide
CCR5 entry inhibitors Maraviroc
In clinical trials: Vicriviroc , Monoclonal Abs: ibilazumab,
PRO140
Integrase inhibitors Raltegravir
In clinical trials: Elvitegravir, S/GSK1349572
Maturation Inhibitors (new class) In clinical trials: Bevirimat and Vivecon (MPC-9055)
*HAART, highly active antiretroviral therapy. Note: This list is likely to be incomplete because new antiretroviral drugs are rapidly being
Abstinence
Monogamous Relationship
Protected Sex
Sterile needles
New shaving/cutting blades
Autoimmune disease
A disease in which the body produces
antibodies that attack its own tissues,
leading to the deterioration and in
some cases to the destruction of such
tissue.
The cause of autoimmune disease is unknown. There
are many theories about what triggers autoimmune
diseases, including:
Bacteria or virus
Drugs
Chemical irritants
Environmental irritants
Treatment
The goals of treatment are to:
•Reduce symptoms
•Control the autoimmune process
•Maintain the body's ability to fight disease
Some patients may need supplements to replace a hormone or vitamin that
the body is lacking. Examples include thyroid supplements, vitamins such as
B12, or insulin injections.
If the autoimmune disorder affects the blood, you may need blood
transfusions.
People with autoimmune disorders that affect the bones, joints, or muscles
may need help with movement or other functions.
Immunosuppressive medicines. Such medicines may include corticosteroids
(such as prednisone) and nonsteroid drugs such as azathioprine,
cyclophosphamide, mycophenolate, sirolimus, or tacrolimus
CHRONIC FATIGUE SYNDROME
A medical condition of unknown cause, with fever, aching,
and prolonged tiredness and depression, typically
occurring after a viral infection.
MAJOR CRITERION
Severe chronic fatigue for ≥ 6 months
 Not due to ongoing exertion or other medical
conditions
 Not substantially relieved by rest
 Significant interference with daily activities
MINOR CRITERION
 Concurrent presence of 4 or more of 8
symptoms:
 Post-exertion malaise lasting > 24 hours
 Unrefreshing sleep
 Impairment of memory or concentration
 Muscle pain
 Pain in multiple joints without swelling or redness
 Headaches of a new type, pattern, or severity
 Tender lymph nodes in the neck or armpit
 Frequent or recurring sore throat that
 For ≥ 6 months  tired most of the time, trouble
concentrating and carrying out daily activities
 Other symptoms include
• mild fever
• lymphadenopathy
• headache
• myalgia
• arthralgia
• depression, and memory loss
• Not caused by ongoing exertion, not relieved by rest
Viral infection
• Ebstein-Barr virus initially proposed
Hypothalamic pituitary adrenal Axis
dysfunction
• Mild hypocortisolism observed in cases of CFS
3. Immunologic basis
• High pro inflammatory cytokines, high IL-1 levels
in CFS
NK cell dysfunction- either decrease in number or
impaired function
• increased levels of T regulatory cells
(CD25+/FOXP3+) CD4 T cells
• Lower activation of CD8 T cells
• Allergies (atopy) and CFS
3. Immunological basis (contd)
• Serotonin and CFS – anti 5-HT autoimmune
activity could play a role in the pathophysiology of
CFS and the onset of physio-somatic symptoms
4. Genetics
• Concordance 55% in monozygotic and 20% in
dizygotic twins
• Sequence variation in genes coding for HTR2A
serotonergic receptor potentially enhancing its activity
may be involved in pathophysiology of CFS
• Differences observed in gene expression in exercise
responsive genes in terms of gene ontology in attempt
to explain fatigue which worsens post exercise in CFS
5. Neuroimaging
 Functional
• Reduced basal ganglia function in terms of decreased
activity of right caudate and right globus pallidus on
fMRI
 Structural
• Reduced grey and white matter volume in the occipital
lobe and reduced grey matter in the right angular
gyrus and right parahippocampal gyrus on VBM in
CFS patients
• Increased prevalence of maladaptive personality
features and personality disorders
• Prevalence of paranoid, schizoid, avoidant, obsessive-
compulsive and depressive personality disorders
significantly higher in CFS compared to normals
• Neuroticism frequently associated with CFS; patients
with CFS were found to be less extraverted
 Impaired information processing speed (reaction
time)
(Cockshell et al, 2013)
 Impaired working memory and poor learning of
information
(Mitchiels 2001)
 Impaired working memory and alterations in
motor speed
(Majer et al.,`2008)
NICE Guidelines (2007)
 General strategies
• Symptom management
• Function and quality of life management (sleep,
rest period, relaxation, pacing, diet)
• Equipment to maintain independence
• Education and employment
 Complementary and supplementary care
 Referral to specialist
 Depression/Anxiety - SSRIs/SNRIsi,e
selective serotonin reuptake inhibitors-
fluoxitine, dapoxitine
 Pain symptoms - TCAs/Duloxetine
 Sleep Disturbance - BZDs/Non-BZD
Hypnotic
Pharmacological interventions for symptom
control
 If chronic pain is a predominant feature - referral
to a pain management clinic
 Prescribing of low-dose tricyclic antidepressants,
specifically amitriptyline, for poor sleep or pain
 Melatonin may be considered for children and
young people with CFS/ME who have sleep
difficulties
(NICE, 2007)
Drugs with some evidence for CFS
• vitamin B1
• vitamin C
• co-enzyme Q10
• magnesium
• NADH (nicotinamide adenine dinucleotide) or
multivitamins and minerals
(NICE, 2007)
Drugs with no evidence in CFS
• monoamine oxidase inhibitors
• glucocorticoids (such as hydrocortisone)
• mineralocorticoids (such as fludrocortisone)
• dexamphetamine
• methylphenidate
• thyroxine
• antiviral agents
(NICE Guidelines, 2007)
• Immunological and Anti-Viral Agent
• Supported by 2 RCTs, awaiting FDA approval
• Acts by stimulating the innate immune system
• Binds to Toll-like Receptor-3 (TLR-3) and
increases production of interferons
• Activates intra-cellular RNAse enzyme – Causes
destruction of viral RNA
(Chambers et al, 2006)
 Graded Exercise Therapy is based on the
model of deconditioning and exercise
intolerance and usually involves
• a home exercise program that continues for 3–5
months.
• Walking or cycling is systematically increased, with set
target heart rates
 The primary component of CBT and GET is a
reduction in fatigue is the change in the
patient's perception of fatigue and focus on
symptoms
LYME’S DISEASE
A form of arthritis caused by bacteria that are
transmitted by ticks.
Causative Organism
Borrelia burgdorferi
Loosely coiled spirochete
8-20 micrometers
 Ixodes scapularis ticks are much smaller than common
dog and cattle ticks
 Below adult female, adult male, nymph, and larva on a
centimeter scale.
 Humans acquire disease from bite of nymphal or adult tick.
Single dose doxycycline shortly after tick
bite.
Lyme disease give doxycycline followed by
amoxacillin
Neuroborreliosis requires IV antibiotic
therapy.
o The brain and spinal cord are covered by connective
tissue layers collectively called the meninges which
form the blood-brain barrier.
1-the pia mater (closest to the CNS)
2-the arachnoid mater
3-the dura mater (farthest from the CNS).
The meninges contain cerebrospinal fluid (CSF).
Meningitis is an inflammation of the meninges, which, if
severe, may become encephalitis, an inflammation
of the brain.
-Bacterial Infections
-Viral Infections
-Fungal Infections
(Cryptococcus neoformans
Coccidiodes immitus)
-Inflammatory diseases
(SLE)
Cancer
-Trauma to head or spine.
One of the physically
demonstrable symptoms
of meningitis is Kernig's
sign. Severe stiffness of
the hamstrings causes
an inability to straighten
the leg when the hip is
flexed to 90 degrees.
DIAGNOSIS
Another physically
demonstrable symptoms
of meningitis is
Brudzinski's sign.
Severe neck stiffness
causes a patient's hips
and knees to flex when
the neck is flexed.
Blood cultures
Examined under a microscope for bacteria
Imaging
X-rays and computerized tomography (CT) scans of
the head, chest or sinuses may reveal swelling or
inflammation
Spinal tap (lumbar puncture)
The definitive diagnosis of meningitis requires an
analysis of your cerebrospinal fluid (CSF), which is
collected during a procedure known as a spinal tap.
In people with meningitis, the CSF fluid often shows
a low sugar (glucose) level along with an increased
white blood cell count and increased protein
TREATMENT
Bacterial meningitis
•Intravenous antibiotics- Gentamycin, Ceftriaxone
•Cortisone medications, to ensure recovery and reduce the risk of
complications, such as brain swelling and seizures.
•The Broad spectrum antibiotic or combination of antibiotics depends
on the type of bacteria causing the infection.
Viral meningitis
•Bed rest
•Plenty of fluids
•Over-the-counter pain medications to help reduce fever and relieve
body aches
•If the cause of your meningitis is a herpes virus, an antiviral
medication
Other types of meningitis
•Fungal meningitis is treated with antifungal medications- Micanozole,
Flucanazole, Itraconazole
•Noninfectious meningitis due to allergic reaction or autoimmune
disease may be treated with cortisone medications
•Cancer-related meningitis requires therapy for the individual cancer.
 The common cold is a viral infection of the
upper respiratory tract
 Usually last approximately 7 days
 Associated with a number of viruses
• Ex. Rhinoviruses, parainfluenza viruses
 Season of the year, age, and prior
exposure are important factors in the type
of virus causing the infection and the type
of symptoms that may occur
Adults have 2-4 colds per year
Children may have up to 10 colds per year
Very contagious
Spread from person to person
Usually from nasal secretions and from
fingers of the affected person
Most contagious in the first 3 days after
symptoms begin
Viruses can last up to 5 hours on the skin
and hard surfaces
Begins with a feeling of dryness and
stuffiness in the nasopharynx (nose)
Nasal secretions (usually clear and watery)
Watery eyes
Red and swollen nasal mucous
membranes
Headache
Generalized tiredness
Chills (in severe cases)
Fever (in severe cases)
Exhaustion (in severe cases)
If the pharynx and larynx (throat) becomes
involved:
• Sore throat
• Hoarseness
Antihistamines
Decongestants
Pain Relievers
Cough suppressants
Nasal Strips
Antibiotics are ineffective!!!
GOOD HANDWASHING!
Cough and sneeze into arm or tissue, not
into your hand
Aerosol sprays (ex. Lysol)
Antibacterial sanitizers (ex. Purell)
Influenza (the flu) is a contagious respiratory illness caused by
influenza viruses. It can cause mild to severe illness, and at times
can lead to death. The best way to prevent seasonal flu is by getting
a seasonal flu vaccination each year.
•In virus classification influenza viruses are RNA viruses that make
up three of the five genera of the family Orthomyxoviridae.
Influenzavirus A
Influenzavirus B
Influenzavirus C
Influenza (the flu)
Influenza A virus
•The type A viruses are the most virulent human pathogens among the three
influenza types and cause the most severe disease. Type A flu or influenza A
viruses are capable of infecting people as well as animals.
•Wild aquatic birds are the natural hosts for a large variety of influenza A.
•The influenza A virus can be subdivided into different serotypes based on the
antibody response to these viruses. The serotypes that have been confirmed in
humans, ordered by the number of known human pandemic deaths, are:
•H1N1, which caused Spanish flu in 1918, and the 2009 flu pandemic
•H2N2, which caused Asian Flu in 1957
•H3N2, which caused Hong Kong Flu in 1968
•H5N1, a current pandemic threat
•H7N7, which has unusual zoonotic potential
•H1N2, endemic in humans and pigs
•H9N2
•H7N2
•H7N3
•H10N7
Influenza B virus
Influenza B almost exclusively infects humans and is less common than
influenza A. This type of influenza mutates at a rate 2–3 times lower than
type A. This reduced rate of antigenic change, combined with its limited
host range ensures that pandemics of influenza B do not occur.
Influenza virus C
Influenza C virus, which infects humans, dogs and pigs, sometimes
causing both severe illness and local epidemics. However, influenza C is
less common than the other types and usually only causes mild disease
in children.
Low pathogenicity (LPAI) - usually only causing mild
respiratory disease in domestic poultry .
High pathogenicity (HPAI) - the more virulent type formerly
known as fowl plague which often results in up to a 100%
flock mortality.
The single best way to prevent seasonal flu is to get a seasonal flu
vaccination each year. There are two types of flu vaccines:
•The "flu shot" : an inactivated vaccine (containing killed virus) that is given
with a needle. The seasonal flu shot is approved for use in people 6 months of
age and older, including healthy people and people with chronic medical
conditions.
•The nasal-spray flu vaccine : a vaccine made with live, weakened flu viruses
that do not cause the flu (sometimes called LAIV for "Live Attenuated
Influenza Vaccine"). LAIV is approved for use in healthy* people 2-49 years of
age who are not pregnant.
About two weeks after vaccination, antibodies develop that protect against
influenza virus infection. Flu vaccines will not protect against flu-like illnesses
caused by non-influenza viruses.
A seasonal flu vaccine will not protect you against the new 2009 H1N1 flu. A
vaccine against the new H1N1 flu is being produced.
Preventing Seasonal Flu: Get Vaccinated
•Vaccinations have been produced to help
fight the spread of influenza A, but because
there are so many strains of the virus,
vaccinations are not always effective or
reliable.
????
Treatment
•Treatment with oseltamivir (trade name Tamiflu®) or zanamivir (trade name
Relenza®) is recommended for all people with suspected or confirmed
influenza who require hospitalization.
 Human Papillomavirus (HPV) is a virus that
can cause various disease states including
“genital” or “venereal” warts
 Papillomaviruses are a complex group of DNA
tumor viruses. They can cause benign
growths (papillomas), cancers, or more
commonly, transient infections
 HPV infection is causally associated with
cervical cancer ; other genital cancers
including anal, penile, vulvar, and vaginal
cancers may have HPV as co-factor
Young age (less than 25 years)
Multiple sex partners
Early age at first intercourse (16 years
or younger)
Male partner has (or has had) multiple
sex partners
Direct skin-to-skin contact
• Usually, but not always sexual contact
Infected birth canal
Fomites (very rare)
 The symptoms may include single or multiple
fleshy growths around the penis, scrotum,
groin, vulva, vagina, anus, and/or urethra
 They may also include: itching, bleeding, or
burning, and pain
 The symptoms may recur from time to time
Source: Cincinnati STD/HIV Prevention
Training Center
Source: CDC/ NCHSTP/ Division of STD Prevention,
STD Clinical Slides
Source: Cincinnati STD/HIV Prevention Training Center
•Risk for penile cancer
•May influence the risk of HPV
acquisition, transmission and
cervical cancer
Source: CDC/NCHSTP/Division of STD, STD Clinical Slides
History
Visual exam
Pap smears
DNA testing
Primary goal for treatment of visible warts
is the removal of symptomatic warts
Therapy may reduce but probably does not
eradicate infectivity
Difficult to determine if treatment reduces
transmission
•No laboratory marker of infectivity
•Variable results utilizing viral DNA
Abstinence
Monogamy
Condoms
Removal of warts
Vaccine (Females aged 9-26)
50% to 70% of sex partners of people
with genital warts already have or do
develop warts.
 Approved in June 2006
• Produced by Merck and Co.
 First vaccine to prevent cervical cancer
 Recombinant vaccine
 Approved for use in females aged 9-26
• Ideally, before becoming sexually active
 Protects against infection with
Types 6, 11, 16, 18
• Women aren’t protected if they have already been
infected with the HPV type(s) that are covered by the
vaccine prior to vaccination
Medicines that can be applied
include podofilox (Condylox) and
trichloroacetic acid (TCA), which kill the
wart tissue, or Aldara, a cream that
stimulates your immune system to fight the
virus.
 Miscellaneous Pneumotrophic Viruses
• Rhinovirus
• Adenovirus
• Respiratory Syncytial Virus
 Miscellaneous Dermotrophic Viruses
• Measles (Rubeola)
• Rubella
• Mumps
• Fifth disease
• Papilloma (HPV)
 Miscellaneous Viscerotrophic Viruses
• Enterovirus (Coxsackie & Echo Viruses)
• Rotavirus
• Norwalk Virus
 Miscellaneous Neurotrophic Viruses
• Poliomyelitis
• Rabies
• Arbovirus
• Arenavirus (lymphocytic choriomeningitis)
 Prion Diseases
• Bovine Spongiform Encephalopathy
• Scrapie
• Creutzfelt-Jakob Syndrome
• Kuru
Immunology and HIV Presentation
Immunology and HIV Presentation

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Immunology and HIV Presentation

  • 1. PRESENTED TO, Mrs. URMILA MISHRA PRESENTED BY, Mr. SAGAR KAMBLE
  • 2.  Immunity is the balanced state of having adequate biological defenses to fight infection, disease, or other unwanted biological invasion, while having adequatetolerance to avoid allergy, and autoimmune diseases.  Immunology is a branch of biomedical science that covers the study of all aspects of the immune system in all organisms. Infection Invasion and multiplication of microorganisms in body tissues, as in an infectious disease.
  • 3.
  • 4. Lymphocytes of the Immune System B Lymphocytes: Immunocompetency occurs in bone marrow Produce Antibodies Conduct Humoral Immunity T Lymphocytes: Immunocompetency occurs in thymus Non antibody producing cells Conduct Cellular Immunity
  • 5.  Antibody Mediated Immunity  Helper T cells recognize non self antigens and stimulate B cells to produce antibodies  B cells release antibodies which bind to non self antigens present on infected cells  B cells complete their maturation upon binding to non self antigens and destroying infected cells  Cell Mediated Immunity  Macrophages phagocytize pathogens  Upon phagocytosis macrophages present non self antigens on their membranes  Helper T cells recognize non self antigens and recruit cytotoxic T cells  Cytotoxic T cells destroy infected cell
  • 6. “Human Immunodeficiency Virus” A unique type of virus (a retrovirus) Invades the helper T cells (CD4 cells) in the body of the host (defense mechanism of a person) Threatening a global epidemic. Preventable, managable but not curable.
  • 7. Former names of the virus include: • Human T cell lymphotrophic virus (HTLV-III) • Lymphadenopathy associated virus (LAV) • AIDS associated retrovirus (ARV)
  • 8.  “Acquired Immunodeficiency Syndrome”  HIV is the virus that causes AIDS  Disease limits the body’s ability to fight infection due to markedly reduced helper T cells. Patients have a very weak immune system (defense mechanism) Patients predisposed to multiple opportunistic infections leading to death.
  • 9.  Acquired immunodeficiency syndrome (AIDS) is a term which applies to the most advanced stages of HIV infection. It is defined by the occurrence of any of more than 20 opportunistic infections or HIV-related cancers.  Persons with positive HIV serology who have ever had a CD4 lymphocyte count below 200 cells/mcL or a CD4 lymphocyte percentage below 14% are considered to have AIDS.
  • 10.
  • 12.  Sharing Needles • Without sterilization Increases the chances of contracting HIV Unsterilized blades
  • 15.
  • 16. Short, flu-like illness - occurs one to six weeks after infection  Mild symptoms  Infected person can infect other people
  • 17. Lasts for an average of ten years This stage is free from symptoms There may be swollen glands The level of HIV in the blood drops to low levels HIV antibodies are detectable in the blood
  • 18. The immune system deteriorates Opportunistic infections and cancers start to appear.
  • 19. The immune system weakens too much as CD4 cells decrease in number.
  • 20. CD4<500 Bacterial infections Tuberculosis (TB) Herpes Simplex Herpes Zoster Vaginal candidiasis Hairy leukoplakia Kaposi’s sarcoma
  • 22. CD4 <50 Disseminated mycobacterium avium complex (MAC) infection Histoplasmosis CMV retinitis CNS lymphoma Progressive multifocal leukoencephalopathy HIV dementia
  • 23.  TB is the most common opportunistic infection in HIV and the first cause of mortality in HIV infected patients (10- 30%)  10 million patients co-infected in the world.  Immunosuppression induced by HIV modifies the clinical presentation of TB : 1. Subnormal clinical and roentgen presentation 2. High rate of MDR/XDR 3. High rate of treatment failure and relapse (5% vs < 1% in HIV)
  • 24.
  • 25.
  • 26. HIV enzyme-linked immunosorbent assay (ELISA) Screening test for HIV Sensitivity > 99.9% Western blot Confirmatory test Speicificity > 99.9% (when combined with ELIZA) HIV rapid antibody test Screening test for HIV Simple to perform Absolute CD4 lymphocyte count Predictor of HIV progression Risk of opportunistic infections and AIDS when <200 HIV viral load tests Best test for diagnosis of acute HIV infection Correlates with disease progression and response to HAART
  • 27. Urine Western Blot • As sensitive as testing blood • Safe way to screen for HIV • Can cause false positives in certain people at high risk for HIV
  • 28. Orasure • The only FDA approved HIV antibody. • As accurate as blood testing • Draws blood-derived fluids from the gum tissue. • NOT A SALIVA TEST!
  • 29.
  • 30.
  • 31. Class of Antiretroviral Drug Drug Names Nucleoside or nucleotide reverse transcriptase inhibitors (NRTIs) Abacavir, emtricitabine (FTC), zidovudine (AZT), didanosine (DDI), zalcitabine (DDC), lamivudine (3TC), tenofovir (disoproxil fumarate), and stavudine (D4T) Nonnucleoside reverse transcriptase inhibitors (NNRTIs) Efavirenz (EFV), etravirine, nevirapine, and delavirdine In clinical trials: Rilpivirine, GSK2248761 (Viiv) and RDEA806 (Ardea) Protease inhibitors (PIs) Amprenavir, atazanavir, darunavir, fosamprenavir, indinavir, lopinavir/ritonavir, nelfinavir (NFV), ritonavir, saquinavir, and tipranavir Pharmacokinetic Enhancers Ritonavir In clinical trials: Cobicistat Fusion entry inhibitors Enfuvirtide CCR5 entry inhibitors Maraviroc In clinical trials: Vicriviroc , Monoclonal Abs: ibilazumab, PRO140 Integrase inhibitors Raltegravir In clinical trials: Elvitegravir, S/GSK1349572 Maturation Inhibitors (new class) In clinical trials: Bevirimat and Vivecon (MPC-9055) *HAART, highly active antiretroviral therapy. Note: This list is likely to be incomplete because new antiretroviral drugs are rapidly being
  • 33.
  • 34. Autoimmune disease A disease in which the body produces antibodies that attack its own tissues, leading to the deterioration and in some cases to the destruction of such tissue. The cause of autoimmune disease is unknown. There are many theories about what triggers autoimmune diseases, including: Bacteria or virus Drugs Chemical irritants Environmental irritants
  • 35.
  • 36.
  • 37. Treatment The goals of treatment are to: •Reduce symptoms •Control the autoimmune process •Maintain the body's ability to fight disease Some patients may need supplements to replace a hormone or vitamin that the body is lacking. Examples include thyroid supplements, vitamins such as B12, or insulin injections. If the autoimmune disorder affects the blood, you may need blood transfusions. People with autoimmune disorders that affect the bones, joints, or muscles may need help with movement or other functions. Immunosuppressive medicines. Such medicines may include corticosteroids (such as prednisone) and nonsteroid drugs such as azathioprine, cyclophosphamide, mycophenolate, sirolimus, or tacrolimus
  • 38. CHRONIC FATIGUE SYNDROME A medical condition of unknown cause, with fever, aching, and prolonged tiredness and depression, typically occurring after a viral infection.
  • 39. MAJOR CRITERION Severe chronic fatigue for ≥ 6 months  Not due to ongoing exertion or other medical conditions  Not substantially relieved by rest  Significant interference with daily activities
  • 40. MINOR CRITERION  Concurrent presence of 4 or more of 8 symptoms:  Post-exertion malaise lasting > 24 hours  Unrefreshing sleep  Impairment of memory or concentration  Muscle pain  Pain in multiple joints without swelling or redness  Headaches of a new type, pattern, or severity  Tender lymph nodes in the neck or armpit  Frequent or recurring sore throat that
  • 41.  For ≥ 6 months  tired most of the time, trouble concentrating and carrying out daily activities  Other symptoms include • mild fever • lymphadenopathy • headache • myalgia • arthralgia • depression, and memory loss • Not caused by ongoing exertion, not relieved by rest
  • 42. Viral infection • Ebstein-Barr virus initially proposed Hypothalamic pituitary adrenal Axis dysfunction • Mild hypocortisolism observed in cases of CFS
  • 43. 3. Immunologic basis • High pro inflammatory cytokines, high IL-1 levels in CFS NK cell dysfunction- either decrease in number or impaired function • increased levels of T regulatory cells (CD25+/FOXP3+) CD4 T cells • Lower activation of CD8 T cells • Allergies (atopy) and CFS
  • 44. 3. Immunological basis (contd) • Serotonin and CFS – anti 5-HT autoimmune activity could play a role in the pathophysiology of CFS and the onset of physio-somatic symptoms
  • 45. 4. Genetics • Concordance 55% in monozygotic and 20% in dizygotic twins • Sequence variation in genes coding for HTR2A serotonergic receptor potentially enhancing its activity may be involved in pathophysiology of CFS • Differences observed in gene expression in exercise responsive genes in terms of gene ontology in attempt to explain fatigue which worsens post exercise in CFS
  • 46. 5. Neuroimaging  Functional • Reduced basal ganglia function in terms of decreased activity of right caudate and right globus pallidus on fMRI  Structural • Reduced grey and white matter volume in the occipital lobe and reduced grey matter in the right angular gyrus and right parahippocampal gyrus on VBM in CFS patients
  • 47. • Increased prevalence of maladaptive personality features and personality disorders • Prevalence of paranoid, schizoid, avoidant, obsessive- compulsive and depressive personality disorders significantly higher in CFS compared to normals • Neuroticism frequently associated with CFS; patients with CFS were found to be less extraverted
  • 48.  Impaired information processing speed (reaction time) (Cockshell et al, 2013)  Impaired working memory and poor learning of information (Mitchiels 2001)  Impaired working memory and alterations in motor speed (Majer et al.,`2008)
  • 49. NICE Guidelines (2007)  General strategies • Symptom management • Function and quality of life management (sleep, rest period, relaxation, pacing, diet) • Equipment to maintain independence • Education and employment  Complementary and supplementary care  Referral to specialist
  • 50.  Depression/Anxiety - SSRIs/SNRIsi,e selective serotonin reuptake inhibitors- fluoxitine, dapoxitine  Pain symptoms - TCAs/Duloxetine  Sleep Disturbance - BZDs/Non-BZD Hypnotic
  • 51. Pharmacological interventions for symptom control  If chronic pain is a predominant feature - referral to a pain management clinic  Prescribing of low-dose tricyclic antidepressants, specifically amitriptyline, for poor sleep or pain  Melatonin may be considered for children and young people with CFS/ME who have sleep difficulties (NICE, 2007)
  • 52. Drugs with some evidence for CFS • vitamin B1 • vitamin C • co-enzyme Q10 • magnesium • NADH (nicotinamide adenine dinucleotide) or multivitamins and minerals (NICE, 2007)
  • 53. Drugs with no evidence in CFS • monoamine oxidase inhibitors • glucocorticoids (such as hydrocortisone) • mineralocorticoids (such as fludrocortisone) • dexamphetamine • methylphenidate • thyroxine • antiviral agents (NICE Guidelines, 2007)
  • 54. • Immunological and Anti-Viral Agent • Supported by 2 RCTs, awaiting FDA approval • Acts by stimulating the innate immune system • Binds to Toll-like Receptor-3 (TLR-3) and increases production of interferons • Activates intra-cellular RNAse enzyme – Causes destruction of viral RNA (Chambers et al, 2006)
  • 55.  Graded Exercise Therapy is based on the model of deconditioning and exercise intolerance and usually involves • a home exercise program that continues for 3–5 months. • Walking or cycling is systematically increased, with set target heart rates  The primary component of CBT and GET is a reduction in fatigue is the change in the patient's perception of fatigue and focus on symptoms
  • 56. LYME’S DISEASE A form of arthritis caused by bacteria that are transmitted by ticks. Causative Organism Borrelia burgdorferi Loosely coiled spirochete 8-20 micrometers
  • 57.  Ixodes scapularis ticks are much smaller than common dog and cattle ticks  Below adult female, adult male, nymph, and larva on a centimeter scale.  Humans acquire disease from bite of nymphal or adult tick.
  • 58. Single dose doxycycline shortly after tick bite. Lyme disease give doxycycline followed by amoxacillin Neuroborreliosis requires IV antibiotic therapy.
  • 59. o The brain and spinal cord are covered by connective tissue layers collectively called the meninges which form the blood-brain barrier. 1-the pia mater (closest to the CNS) 2-the arachnoid mater 3-the dura mater (farthest from the CNS). The meninges contain cerebrospinal fluid (CSF). Meningitis is an inflammation of the meninges, which, if severe, may become encephalitis, an inflammation of the brain.
  • 60. -Bacterial Infections -Viral Infections -Fungal Infections (Cryptococcus neoformans Coccidiodes immitus) -Inflammatory diseases (SLE) Cancer -Trauma to head or spine.
  • 61.
  • 62. One of the physically demonstrable symptoms of meningitis is Kernig's sign. Severe stiffness of the hamstrings causes an inability to straighten the leg when the hip is flexed to 90 degrees. DIAGNOSIS
  • 63. Another physically demonstrable symptoms of meningitis is Brudzinski's sign. Severe neck stiffness causes a patient's hips and knees to flex when the neck is flexed.
  • 64. Blood cultures Examined under a microscope for bacteria Imaging X-rays and computerized tomography (CT) scans of the head, chest or sinuses may reveal swelling or inflammation Spinal tap (lumbar puncture) The definitive diagnosis of meningitis requires an analysis of your cerebrospinal fluid (CSF), which is collected during a procedure known as a spinal tap. In people with meningitis, the CSF fluid often shows a low sugar (glucose) level along with an increased white blood cell count and increased protein
  • 65. TREATMENT Bacterial meningitis •Intravenous antibiotics- Gentamycin, Ceftriaxone •Cortisone medications, to ensure recovery and reduce the risk of complications, such as brain swelling and seizures. •The Broad spectrum antibiotic or combination of antibiotics depends on the type of bacteria causing the infection. Viral meningitis •Bed rest •Plenty of fluids •Over-the-counter pain medications to help reduce fever and relieve body aches •If the cause of your meningitis is a herpes virus, an antiviral medication Other types of meningitis •Fungal meningitis is treated with antifungal medications- Micanozole, Flucanazole, Itraconazole •Noninfectious meningitis due to allergic reaction or autoimmune disease may be treated with cortisone medications •Cancer-related meningitis requires therapy for the individual cancer.
  • 66.  The common cold is a viral infection of the upper respiratory tract  Usually last approximately 7 days  Associated with a number of viruses • Ex. Rhinoviruses, parainfluenza viruses  Season of the year, age, and prior exposure are important factors in the type of virus causing the infection and the type of symptoms that may occur
  • 67. Adults have 2-4 colds per year Children may have up to 10 colds per year
  • 68. Very contagious Spread from person to person Usually from nasal secretions and from fingers of the affected person Most contagious in the first 3 days after symptoms begin Viruses can last up to 5 hours on the skin and hard surfaces
  • 69. Begins with a feeling of dryness and stuffiness in the nasopharynx (nose) Nasal secretions (usually clear and watery) Watery eyes Red and swollen nasal mucous membranes Headache Generalized tiredness Chills (in severe cases)
  • 70. Fever (in severe cases) Exhaustion (in severe cases) If the pharynx and larynx (throat) becomes involved: • Sore throat • Hoarseness
  • 72. GOOD HANDWASHING! Cough and sneeze into arm or tissue, not into your hand Aerosol sprays (ex. Lysol) Antibacterial sanitizers (ex. Purell)
  • 73. Influenza (the flu) is a contagious respiratory illness caused by influenza viruses. It can cause mild to severe illness, and at times can lead to death. The best way to prevent seasonal flu is by getting a seasonal flu vaccination each year. •In virus classification influenza viruses are RNA viruses that make up three of the five genera of the family Orthomyxoviridae. Influenzavirus A Influenzavirus B Influenzavirus C Influenza (the flu)
  • 74. Influenza A virus •The type A viruses are the most virulent human pathogens among the three influenza types and cause the most severe disease. Type A flu or influenza A viruses are capable of infecting people as well as animals. •Wild aquatic birds are the natural hosts for a large variety of influenza A. •The influenza A virus can be subdivided into different serotypes based on the antibody response to these viruses. The serotypes that have been confirmed in humans, ordered by the number of known human pandemic deaths, are: •H1N1, which caused Spanish flu in 1918, and the 2009 flu pandemic •H2N2, which caused Asian Flu in 1957 •H3N2, which caused Hong Kong Flu in 1968 •H5N1, a current pandemic threat •H7N7, which has unusual zoonotic potential •H1N2, endemic in humans and pigs •H9N2 •H7N2 •H7N3 •H10N7
  • 75. Influenza B virus Influenza B almost exclusively infects humans and is less common than influenza A. This type of influenza mutates at a rate 2–3 times lower than type A. This reduced rate of antigenic change, combined with its limited host range ensures that pandemics of influenza B do not occur. Influenza virus C Influenza C virus, which infects humans, dogs and pigs, sometimes causing both severe illness and local epidemics. However, influenza C is less common than the other types and usually only causes mild disease in children.
  • 76.
  • 77.
  • 78. Low pathogenicity (LPAI) - usually only causing mild respiratory disease in domestic poultry . High pathogenicity (HPAI) - the more virulent type formerly known as fowl plague which often results in up to a 100% flock mortality.
  • 79.
  • 80.
  • 81.
  • 82.
  • 83.
  • 84.
  • 85. The single best way to prevent seasonal flu is to get a seasonal flu vaccination each year. There are two types of flu vaccines: •The "flu shot" : an inactivated vaccine (containing killed virus) that is given with a needle. The seasonal flu shot is approved for use in people 6 months of age and older, including healthy people and people with chronic medical conditions. •The nasal-spray flu vaccine : a vaccine made with live, weakened flu viruses that do not cause the flu (sometimes called LAIV for "Live Attenuated Influenza Vaccine"). LAIV is approved for use in healthy* people 2-49 years of age who are not pregnant. About two weeks after vaccination, antibodies develop that protect against influenza virus infection. Flu vaccines will not protect against flu-like illnesses caused by non-influenza viruses. A seasonal flu vaccine will not protect you against the new 2009 H1N1 flu. A vaccine against the new H1N1 flu is being produced. Preventing Seasonal Flu: Get Vaccinated
  • 86. •Vaccinations have been produced to help fight the spread of influenza A, but because there are so many strains of the virus, vaccinations are not always effective or reliable.
  • 87. ????
  • 88. Treatment •Treatment with oseltamivir (trade name Tamiflu®) or zanamivir (trade name Relenza®) is recommended for all people with suspected or confirmed influenza who require hospitalization.
  • 89.  Human Papillomavirus (HPV) is a virus that can cause various disease states including “genital” or “venereal” warts  Papillomaviruses are a complex group of DNA tumor viruses. They can cause benign growths (papillomas), cancers, or more commonly, transient infections  HPV infection is causally associated with cervical cancer ; other genital cancers including anal, penile, vulvar, and vaginal cancers may have HPV as co-factor
  • 90. Young age (less than 25 years) Multiple sex partners Early age at first intercourse (16 years or younger) Male partner has (or has had) multiple sex partners
  • 91. Direct skin-to-skin contact • Usually, but not always sexual contact Infected birth canal Fomites (very rare)
  • 92.  The symptoms may include single or multiple fleshy growths around the penis, scrotum, groin, vulva, vagina, anus, and/or urethra  They may also include: itching, bleeding, or burning, and pain  The symptoms may recur from time to time
  • 93. Source: Cincinnati STD/HIV Prevention Training Center Source: CDC/ NCHSTP/ Division of STD Prevention, STD Clinical Slides
  • 94. Source: Cincinnati STD/HIV Prevention Training Center
  • 95. •Risk for penile cancer •May influence the risk of HPV acquisition, transmission and cervical cancer
  • 96. Source: CDC/NCHSTP/Division of STD, STD Clinical Slides
  • 98. Primary goal for treatment of visible warts is the removal of symptomatic warts Therapy may reduce but probably does not eradicate infectivity Difficult to determine if treatment reduces transmission •No laboratory marker of infectivity •Variable results utilizing viral DNA
  • 99. Abstinence Monogamy Condoms Removal of warts Vaccine (Females aged 9-26) 50% to 70% of sex partners of people with genital warts already have or do develop warts.
  • 100.
  • 101.  Approved in June 2006 • Produced by Merck and Co.  First vaccine to prevent cervical cancer  Recombinant vaccine  Approved for use in females aged 9-26 • Ideally, before becoming sexually active  Protects against infection with Types 6, 11, 16, 18 • Women aren’t protected if they have already been infected with the HPV type(s) that are covered by the vaccine prior to vaccination
  • 102. Medicines that can be applied include podofilox (Condylox) and trichloroacetic acid (TCA), which kill the wart tissue, or Aldara, a cream that stimulates your immune system to fight the virus.
  • 103.  Miscellaneous Pneumotrophic Viruses • Rhinovirus • Adenovirus • Respiratory Syncytial Virus
  • 104.  Miscellaneous Dermotrophic Viruses • Measles (Rubeola) • Rubella • Mumps • Fifth disease • Papilloma (HPV)
  • 105.  Miscellaneous Viscerotrophic Viruses • Enterovirus (Coxsackie & Echo Viruses) • Rotavirus • Norwalk Virus
  • 106.  Miscellaneous Neurotrophic Viruses • Poliomyelitis • Rabies • Arbovirus • Arenavirus (lymphocytic choriomeningitis)
  • 107.  Prion Diseases • Bovine Spongiform Encephalopathy • Scrapie • Creutzfelt-Jakob Syndrome • Kuru