HIV Flashcards

(26 cards)

1
Q

Describe the characteristics of retroviruses

A
  1. Subfamilies of retroviruses
    a) Oncoviruses (HTLV-1, HTLV-2)
    b) Lentiviruses (HIV-1, HIV-2)
  2. AIDS
    a) HIV positive, less than 200 CD4 cells, or an AIDS indicator disease
  3. Enveloped, positive-strand RNA virus that encodes reverse transcriptase
  4. Replicate through a DNA intermediate
  5. The DNA copy is integrated into the host chromosome to become a cellular gene
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2
Q

What are the charateristics of retroviruseswhere and who discovered retrovirus

A
  1. HIV-1 discovered in 1981 by Gallo and Montagnier
  2. Subsequently, HIV-2 was isolated in West Africa
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3
Q

Describe the epidemiology of Retrovirus (HIV)

A
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4
Q

Where is HIV present

A
  1. In blood (or fluids contaminated by blood and serum)
  2. semen
  3. vaginal fluids
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5
Q

Describe the host related factors that can increases the infectiousness of HIV

A
  1. primary infection – high viral load
  2. late-stage infection – high viral load
  3. genital tract infections – mucosal breech and recruitment of inflammatory cells
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6
Q

What is the percentage of people who do not know they have HIV

A

approx 15%

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7
Q

what is the percentage of children who obtain HIV from their mother

A

1 in 4 = 25%

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8
Q

what is the percentage of children who obtain HIV from their mother with older Tx

A

4%

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9
Q

what is the percentage of children who obtain HIV from their mother with HAART Tx

A

less than o.5%

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10
Q

How does HIV replicate

A
  1. gp120 interacts with the CD4 surface molecule expressed on helper T lymphocytes and cells of macrophage lineage = macrophages, dendritic cells, and microglial cells (brain cells)
  2. HIV enters the cell by fusion with the cellular envelope
  3. After release, the reverse transcriptase
    synthesizes a complementary DNA strand
  4. A copy of the DNA strand is then produced
  5. Integrated into our genome by Integrase; Once integrated, viral DNA is transcribed like
    other host genes
  6. Each copy contains approximately five errors
    or mutations
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11
Q

What does HIV infection of CD$ lymphocytes result in and how

A
  1. results in cell death by a direct effect or by apoptosis (programmed cell death)
  2. loss of cell mediates immunity and in opportunistic and malignancies occur
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12
Q

when does aids develop

A

when any number of signs of CD4 depletion occur

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13
Q

describe the signs of CD4 depletion for opportunistic infections

A
  1. oral candidiasis
  2. toxoplasmosis
  3. cryptococcal meningitis
  4. severe herpes infections
  5. cytomegalovirus infections
  6. tuberculosis
  7. Pneumocystis pneumonia
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14
Q

describe the signs of CD4 depletion for Maligancies

A
  1. Kaposi’s sarcoma
  2. Lymphoma
  3. Cervical cancer
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15
Q

Besides opportunistic infections and malignancies what are other signs of signs of CD4 depletion

A
  1. Aids related dementia
  2. wasting syndrome
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16
Q

what is the window period for HIV mean

A

time between infection and lab detection

17
Q

what does seroconversion mean

A

HIV-infected patients will eventually generate anti-HIV antibodies

18
Q

How do you test for HIV

A
  1. If testing occurs too early, the result will be falsely negative …test over time
  2. If HIV screen is positive …confirm the result to avoid false positives
  3. Two-tiered serologic testing
19
Q

How do you screen for HIV

A
  1. By using Enzyme immunoassay (EIA) or chemiluminescent microparticle immunoassay (CMIA)
    a) 4th generation assays detect both HIV antigen and antibodies
  2. Serology
    a) tests for antibodies to viral antigens by enzyme immunoassays
  3. Immunologic studies
    a) CD4 counts
  4. Viral load testing
    a) PCR quantification of RNA in plasma
  5. Resistance genotyping
    a) looking at the sequences of the genes in the
    HIV to see if there are mutations that cause resistance
20
Q

What are the advantages of HIV-1 / HIV-2 immunoblot (confirmatory)

A
  1. Rapid – 30 min.
  2. More specific
  3. Confirmation of both HIV-1 and HIV-2
21
Q

what are the goals of HIV therapy

A
  1. Maximal and durable suppression viral load
  2. Restoration or preservation of immune function
  3. Improvement in quality of life
  4. Reduction of HIV morbidity & mortality
  5. Preservation of future treatment options
22
Q

wjhat is Quantitative RT-PCR (“viral load”) used for in HIV

A

Used to monitor antiretroviral therapy over time

23
Q

During a needle stick exposure of HIV what does the risk of infectiondepend on

A
  1. Stage of the patient’s disease
  2. How much blood (hollow vs solid, gauge of needle, aspiration vs injection)
24
Q

what do you do if you have a needle stick exposure of HIV

A
  1. Confirm patient’s status
  2. Document your status
  3. Begin antiviral prophylaxis
25
To be effective PPE must begin within how many hours
72 hours of exposure 2hrs of exposure best
26