HIV infections and Aids Flashcards

1
Q

What does AIDS stand for?

A

Acquired Immunodeficiency syndrome

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2
Q

What is AIDS?

A
  • An anthroponotic disease
  • last stage of infection with Human immunodeficiency virus /HIV/
  • presented by severe and irreversible immune deficiency leading to opportunistic infections and/or neoplasma occurrence
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3
Q

What family is the HIV virus from?

A

subfamily Lentiviridae, family Retroviridae

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4
Q

What are the two types of known HIV viruses?

A

Two types of HIV viruses are known, causing similar signs and symptoms:

HIV1 – distributed all over the world
HIV2 – endemic for West Africa

Low resistance of the virus in the environment

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5
Q

What is an anthroponotic disease?

A

Anthroponoses (Greek “anthrópos” = man, “nosos” = disease) are diseases transmissible from human to human. Examples include rubella, smallpox, diphtheria, gonorrhea, ringworm (Trichophyton rubrum), and trichomoniasis. Zoonoses (Greek “zoon” = animal) are diseases transmissible from living animals to humans

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6
Q

What is the source of infection of HIV?

A

Source of infection: infected person or carriers – 10-100 days after infection to the end of their life

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7
Q

What does the risk of infection depend on for HIV?

A

The risk for infection depends on the viral load in the source

Highest concentration of the virus in semen, vaginal secretions, blood, and CSF /just in those with neurological involvement/

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8
Q

What are the modes of transmission for HIV?

A
  • Sexual contact
  • Blood route
  • Vertical transmission
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9
Q

How is HIV contracted by sexual contact?

A

More than 70% of the cases

Homosexual or heterosexual contact without protection by condoms

Easier way for infection of women after contact with infected men than the opposite

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10
Q

How is HIV transmitted through the blood route?

A

About 15% of cases

Realized by: blood transfusion, medical manipulations using contaminated tools, iv drug users, tattoo, shaving by contaminated razor, work with HIV infected /0,03%/

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11
Q

How is HIV transmitted vertically?

A

From infected mother to child
Low risk – 15-20%
Risk period: at the time of delivery
Infections of the child by breastfeeding in 30-50%

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12
Q

Where is AIDS most prominent?

A

About 42 million people are infected by HIV worldwide /1% of the global adult population aged 15-49 years/

Majority of infections remain in sub-Saharan Africa, where 5.2% of the population is thought to be infected

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13
Q

What is the prognosis for untreated HIV infection?

A

The prognosis in patients with untreated HIV infection is poor, with an overall mortality rate of more than 90% for an average period varying between 8-10 years after infection

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14
Q

Which are the target cells for HIV?

A

Cells, which express on their surface CD4 receptor:

Immune cells: 60% of T-lymphocytes /CD4 lymphocytes or so called T-helpers mainly/, monocytes, macrophages

Cells of the nervous system: astrocytes, glyocytes, dendritic cells

Organ cells: kidneys, hepatocytes, enterocytes, cardiocytes, Langerhans cells in the skin

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15
Q

What is the pathogenesis of HIV?

A
  • Adherence between viral protein gp120 and different cells, which express CD4
  • Penetration of the virus in the target cells mediated by fusion between gp-41 and cell membrane
  • Viral replication in the target cells
  • Integration of the provirus into the cells’ genome by integrases and replication together with cell’s DNA, producing new virions
  • The new synthesized viruses are separated by proteases to new HIV viruses
  • Death of the infected cells by lysis, syncytium formation, apoptosis
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16
Q

How does HIV cause immunosuppression?

A

Progressive death of CD4 leads to progression of immunosuppression and viral load increases again

/highest level at the end stage of the disease/=AIDS
development when patients are susceptible to opportunistic infections and malignancies

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17
Q

What is the mechanism of immunosuppression in HIV?

A

Damage and death of TCD4 mainly /referent range about 500/mm3

Depressed function of monocytes and macrophages – ineffective phagocytosis

TCD8 /T-suppressors/ - increased level in the beginning of the disease, leading to CD4:CD8<0,5. In the late stages – decreasing of CD8 number and CD4:CD8 becomes false normal but severe immunosuppression is presented at that time

B cells – production of anti HIV antibodies, which does not have protective functions, just important for the diagnosis

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18
Q

What are the different phases seen in AIDS?

A
  • Early phase (acute retroviral syndrome, primary clinical complex)
  • Asymptomatic phase (latent, chronic)
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19
Q

What is involved in the early phase?

A

3-6 weeks after infection

50-70% of patients – flu like symptoms: fever, weakness, muscle pain, sore throat, lymphadenopathy

/DD with inf. mononucleosis/, hepatomegaly, splenomegaly, rash, encephalopathy

WBC: leucocytosis, lymphocytosis,

High viral load with normal TCD4, positive p24 antigen, negative ELISA /’serological window’/

Infected person is contagious

Duration: 2-4 weeks and self-limiting course
At the end of this period - appearance of antibodies in the serum together with decreasing of viral load to the set point

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20
Q

What is involved in the asymptomatic/ latent/ chronic phase?

A

Duration: 7-16 years and it depends on:
Co-occurrence of another sexual-transmitted diseases
Pregnancy
Co-infection with EBV/HHV6
Iv drug users
Smokers/chronic alcocholism
HLA predilection:
B11, 27, 51, 57, 58 – slow progression
A23, B37 – fast progression

Lack of any symptoms

Progressive: decreasing of TCD4 count <500/mm3 and increasing of viral load

Patients are seropositive

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21
Q

What is the clinical presentation of AIDS?

A

At the end of second stage
First indicators: persistent enlarged lymph nodes

Low-grade fever

Sweating

Chronic diarrhea

Oropharyngeal candidiasis (thrush)

Vulvovaginal candidiasis, persistent or resistant
Hairy leukoplakia

Herpes zoster (shingles), involving two or more episodes or at least one dermatome

Peripheral neuropathy, Aseptic meningitis

Kaposi’s sarcoma

Ca coli uteri

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22
Q

When is Kaposi’s sarcoma observed in AIDS patients?

A

In 20% of patients with AIDS
Caused by HHV8
Observed mostly in homosexuals and its relative incidence is declining

23
Q

What are some AIDS-defining clinical conditions?

A
  • Opportunistic infections
  • Malignancies
  • HIV associated encephalopathy
24
Q

What is an opportunistic pathogen?

A
  • An opportunistic infection is an infection caused by pathogens (bacteria, viruses, fungi, or protozoa) that take advantage of an opportunity not normally available
  • such as a host with a weakened immune system, an altered microbiota (such as a disrupted gut flora), or breached integumentary barriers.
  • Many of these pathogens do not cause disease in a healthy host that has a normal immune system
25
Q

What are some parasite-caused AIDS-defining clinical conditions?

A

PCP – severe pneumonia
T. gondii – encephalitis; myocarditis, generalized lymphadenitis
T. gondii – encephalitis; myocarditis, generalized lymphadenitis

26
Q

What are some mycosis-caused AIDS-defining clinical conditions?

A

C. albicans – oropharyngeal, eosophageal, sepsis
C. neoformans – meningitis
H. capsulatum – sepsis, pneumonia

27
Q

What are some virus-caused AIDS-defining clinical conditions?

A

CMV – pneumonia, hepatitis, encephalitis, retinitis

HSV – encephalitis, oral and anal vesicles

VZV – chickenpox or shingles with hemorrhagic fluid

EBV – leucoencephalopathy, hepatitis, Burkitt - lymphoma

28
Q

What are some bacteria-caused AIDS-defining clinical conditions?

A

TB

MAC – disseminated form, gastrointestinal inflammation, pulmonary inflammation, skin changes

Staph, Str, and other coccus

T. pallidum

29
Q

What are some malignancies that are AIDS-defining conditions?

A

Kaposi’s Sarcoma
Non – Hodgkin lymphoma
Carcinoma spinocellulare
Carcinoma basocellulare
Melanoma malignum

30
Q

What are the criteria for AIDS?

A

HIV /+/ plus: CD4<200/mm3 or CD4<14% of total lymphocyte count or 1 or occurrence of one or more of the AIDS-defining clinical conditions

31
Q

Which test is used to screen for HIV?

A

HIV enzyme-linked immunosorbent assay (ELISA)
> 99.9% sensitivity

32
Q

Which test is used as a confirmatory test for HIV?

A

Western blot test
> 99.9% specificity (when combined with ELISA)

33
Q

Which test is a predictor of HIV progression?

A

Absolute CD4 lymphocyte count
risk for opportunistic infections and AIDS when <200

34
Q

Which is the best diagnosis method for acute HIV infection?

A

HIV viral load tests
correlates with disease progression and corresponds to HAART

35
Q

What are the aims of treatment?

A

To provide longer and qualitative life

To delay the progression of the disease

To ‘recover’ the patients’ immune system

To reduce the HIV transmission

36
Q

What are the general principles of treatment?

A

Complex therapy
HAART
Immunostimulation
Treatment of opportunistic infections and malignancies

37
Q

What does HAART stand for?

A

highly active antiretroviral therapy

38
Q

What is HAART?

A

Using ART makes AIDS chronic disease

Treatment to the end of the patient’s life

Reduces the mortality with 49%

Starts when the diagnosis is proved

Associated with immune reconstitution inflammatory syndrome (IRIS) in some patients - paradoxical worsening of an existing infection or disease process or appearance of a new infection/disease process soon after initiation of therapy

Combined therapy – min two drugs

39
Q

What are the different classes of drugs used in HAART?

A

Reverse Transcriptase inhibitors

Protease inhibitors

Integrase inhibitors

Fusion inhibitors

40
Q

What are the different classes of drugs used in HAART?

A

Reverse Transcriptase inhibitors

Protease inhibitors

Integrase inhibitors

Fusion inhibitors

41
Q

What are some examples of reverse transcriptase inhibitors?

A

Nucleoside analogue /NRTI/:
Zidovudine, Lamivudine, Stavudine, Abacavir, Tenofovir

Non-Nucleoside Transcriptase inhibitors /NNRTI/:
Nevirapine, Delavirdine, Efavirenz

42
Q

What are some examples of protease inhibitors?

A

Ritonavir, Atazanavir, Lopinavir /+Ritonavir=Caletra/, Indinavir, Darunavir

42
Q

What are some examples of protease inhibitors?

A

Ritonavir, Atazanavir, Lopinavir /+Ritonavir=Caletra/, Indinavir, Darunavir

43
Q

What are some examples of integrase inhibitors?

A

Raltegravir

44
Q

What are some examples of integrase inhibitors?

A

Raltegravir

45
Q

What are some examples of fusion inhibitors?

A

Enfuviritide, Maraviroc

46
Q

What are some health care follow up measures that must be followed for patients infected with HIV?

A

CD4 counts every 3–6 months

Viral load tests every 3–6 months and 1 month following a change in therapy

PPD

Izoniazide for those with positive PPD and normal chest radiograph

VDRL/TPHL for syphilis

Toxoplasma IgG serology

CMV IgG serology

Pneumococcal vaccine

Influenza vaccine in season

Hepatitis B vaccine for those who are HBsAg-negative

Haemophilus influenzae type b vaccination

Papanicolaou smears every 6 months for women

47
Q

What infection are HIV-patients with CD4 < 200 cells/mm3 at risk for? and what is the prophylaxis?

A

Pneumocystis jiroveci prophylaxis – TMP/SMZ

48
Q

What infection are HIV-patients with CD4 < 75 cells/mm3 at risk for? and what is the prophylaxis?

A

Mycobacterium avium complex prophylaxis – macrolides

49
Q

What infection are HIV-patients with CD4 < 50 cells/mm3 at risk for? and what is the prophylaxis?

A

Consider CMV prophylaxis - ganciclovir

50
Q

What prophylactic measures can be taken against HIV infection?

A

Avoidance of risk sexual contacts

Stopping the use of iv. drugs or using sterile needles

Circumcision in men reduces the risk for HIV infection with 50%

Screening of the blood banks

Perinatal prophylaxis

51
Q

What is Pre-exposure prophylaxis (PrEP) ?

A

reduces the risk of getting HIV from sex by more than 90%; combination of two HIV medicines (tenofovir and emtricitabine), sold under the name Truvada®

52
Q

What is Post-exposure prophylaxis (PEP) ?

A

must be started within 72 hours after a recent possible exposure to HIV, 28 days, Tenofovir combined with either lamivudine (3TC) or emtricitabine (FTC)