immune dysfunction

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primary cells are -

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1

primary cells are -

leukocytes

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2

where are leukocytes stored?

thymus, spleen, bone marrow

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3

what are the two types of immune cells?

phagocytes (eat) and lymphocytes (develop antibodies)

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4

B cells -

produce antibodies

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5

T cells -

destroy antibodies

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6

when is IgG at mature levels?

8 years

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7

when is IgM at mature levels?

1 year

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8

when is IgA and IgE at mature levels?

6 years

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9

what are changes to the lifestyle made by immunosuppressed children?

no live vaccines, no plants/flowers, neutropenic diet followed

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10

a group of rare congenital disorders characterized by absence of both T and B cells

severe combined immunodeficiency (SCID)

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11

what increases an individuals risk for SCID?

consanguineous marriage (intermarriage)

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12

a child presents with constant infections, failure to thrive, and small thymus, minimal tonsils and lymph nodes - what do suspect?

SCID

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13

what is the primary treatment for SCID?

hematopoietic stem cell transplant within the first 3 months of life

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14

what is some additional treatment for SCID?

gene therapy, thymus transplant, enzyme replacement

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15

retrovirus that attacks the immune system by destroying T lymphocytes

HIV

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16

what labs will you monitor in a child with HIV?

low WBCs and low T cell counts

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17

when a HIV positive woman is pregnant and give birth, what do you assume about the fetus?

they they also have HIV until proven otherwise

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18

what interventions have prevented transmission of HIV during pregnancy?

taking antiretroviral medications throughout pregnancy, elective C sections

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19

an infant commonly getting candidiasis is a sign of -

HIV

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20

what is a common sign of HIV in older children?

recurrent bacterial infections

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21

how is HIV treated?

a combination of at least 3 antiretroviral drugs from at least 2 categories

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22

joint inflammation lasting longer than 6 weeks with no identifiable cause with an onset occurring at younger than 16 years of age indicates -

juvenile idiopathic arthritis (JIA)

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23

when are the two peaks of JIA?

preschool aged, adolescence

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24

what are the two studies used to diagnosed JIA?

ESR and CRP

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25

what is a non pharmalogical treatment of JIA?

physical therapy and range-of-motion exercises

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26

what are common medications used to treat JIA?

NSAIDs, methotrexate, steroids, biologic response modifiers

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27

the immune system identifies body tissue as foreign -

systemic lupus erythematosus

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28

butterfly rash, fever, fatigue, hypertension, and abdominal pain are all common symptoms of -

lupus

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29

what is a serious complication associated with lupus?

multiorgan failure

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30

what is a common trigger of lupus?

the dark/ultraviolet light

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31

what are diagnostic studies used for lupus?

ANA and LE

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32

what is the goal of lupus treatment?

preventing outbreaks, treating outbreaks when they do happen, and preventing organ damage

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33

what drugs are given to treat lupus initially?

NSAIDS and antimalarial drugs

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34

what drugs are given later on in lupus treatment?

steroids and methotrexate

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35

what medications are given to treat the neurologic symptoms of lupus?

immunosuppressive medications, antidepressants, antiepileptics

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36

what does skin testing for allergies measure?

allergen specific IgE

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37

what are some recommendations for treating insect stings and allergies?

cold compress, antipruritic (antihistamines), corticosteroids

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